ClinVar for Gene (Select 79153) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063436	GRCh37/hg19 16p11.2(chr16:29427215-30177240)x1	ALDOA, ASPHD1 +27 more	Copy number loss	not specified	GPathogenic
Select item 3063430	GRCh37/hg19 16p11.2(chr16:29383808-30191848)x1	ALDOA, ASPHD1 +27 more	Copy number loss	not specified	GPathogenic
Select item 3063416	GRCh37/hg19 16p11.2(chr16:29432212-30178406)x1	ALDOA, ASPHD1 +27 more	Copy number loss	not specified	GPathogenic
Select item 3062345	GRCh38/hg38 16p11.2(chr16:29642391-30204353)	LOC121587541, LOC121847976 +105 more	Copy number loss	Epilepsy syndrome	GPathogenic, low penetrance
Select item 3024604	GRCh37/hg19 16p11.2(chr16:29495010-30200397)x1	ALDOA, ASPHD1 +25 more	Copy number loss	not provided	GPathogenic
Select item 3024603	GRCh37/hg19 16p11.2(chr16:29472703-30256894)x1	ALDOA, ASPHD1 +29 more	Copy number loss	not provided	GPathogenic
Select item 3024180	GRCh38/hg38 16p11.2(chr16:29329272-30178707)x1	LOC130058763, LOC130058764 +107 more	Copy number loss	Proximal 16p11.2 microdeletion syndrome	GPathogenic
Select item 2685573	GRCh37/hg19 16p11.2(chr16:29589674-30226930)x1	ALDOA, ASPHD1 +28 more	Copy number loss	not provided	GPathogenic
Select item 2685572	GRCh37/hg19 16p11.2(chr16:29517698-30191848)x1	ALDOA, ASPHD1 +24 more	Copy number loss	not provided	GPathogenic
Select item 2685571	GRCh37/hg19 16p11.2(chr16:29432213-30226930)x1	ALDOA, ASPHD1 +31 more	Copy number loss	not provided	GPathogenic
Select item 2685568	GRCh37/hg19 16p11.2(chr16:29343245-30240227)x1	ALDOA, ASPHD1 +31 more	Copy number loss	not provided	GPathogenic
Select item 2684804	GRCh37/hg19 16p11.2(chr16:29654589-30177240)x3	ALDOA, ASPHD1 +24 more	Copy number gain	not provided	GPathogenic
Select item 2684803	GRCh37/hg19 16p11.2(chr16:29597823-30321320)x3	ALDOA, ASPHD1 +28 more	Copy number gain	not provided	GPathogenic
Select item 2672674	GRCh37/hg19 16p11.2(chr16:29495010-30212427)x1	SLX1A, SULT1A3 +28 more	Copy number loss	not provided	GPathogenic
Select item 2671579	Single allele	ALDOA, ASPHD1 +25 more	Duplication	not provided	GPathogenic
Select item 2618765	NM_024307.3(GDPD3):c.490G>A (p.Gly164Ser)	GDPD3 (G164S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2582950	GRCh37/hg19 16p11.2(chr16:29674568-30199897)x3	QPRT, SEZ6L2 +25 more	Copy number gain	not provided	GPathogenic
Select item 2580337	GRCh37/hg19 16p11.2(chr16:29517464-30200058)x1	ALDOA, ASPHD1 +25 more	Copy number loss	Distal 16p11.2 microdeletion syndrome	GPathogenic
Select item 2580331	GRCh37/hg19 16p11.2(chr16:29517464-30199839)x1	ALDOA, ASPHD1 +25 more	Copy number loss	Distal 16p11.2 microdeletion syndrome	GPathogenic
Select item 2580320	GRCh37/hg19 16p11.2(chr16:29517464-30200058)x3	ALDOA, ASPHD1 +25 more	Copy number gain	Distal 16p11.2 microdeletion syndrome	GPathogenic
Select item 2580312	GRCh37/hg19 16p11.2(chr16:29511270-30243006)x1	ALDOA, ASPHD1 +28 more	Copy number loss	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20	GPathogenic
Select item 2576522	GRCh37/hg19 16p11.2(chr16:29656684-30197341)x1	ALDOA, ASPHD1 +28 more	Copy number loss	Proximal 16p11.2 microdeletion syndrome	GPathogenic
Select item 2570962	GRCh37/hg19 16p11.2(chr16:29675050-30218384)x1	C16orf92, KIF22 +28 more	Copy number loss	not provided	GPathogenic
Select item 2561319	NM_024307.3(GDPD3):c.893C>T (p.Thr298Met)	GDPD3, YPEL3-DT (T298M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2514022	NM_024307.3(GDPD3):c.392G>A (p.Arg131His)	GDPD3 (R73H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2506560	GRCh37/hg19 16p11.2(chr16:29495011-30206548)	ALDOA, ASPHD1 +27 more	Copy number loss	Infantile convulsions and choreoathetosis	GPathogenic
Select item 2499634	GRCh38/hg38 16p11.2(chr16:29653297-30181026)	ALDOA, ASPHD1 +90 more	Copy number loss	See cases	GPathogenic
Select item 2492363	NM_024307.3(GDPD3):c.619G>T (p.Val207Leu)	GDPD3 (V149L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2485302	NM_024307.3(GDPD3):c.806A>C (p.Glu269Ala)	GDPD3 (E269A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2454813	NM_024307.3(GDPD3):c.757G>C (p.Val253Leu)	GDPD3 (V195L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2388717	NM_024307.3(GDPD3):c.811G>A (p.Gly271Arg)	GDPD3 (G213R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377832	NM_024307.3(GDPD3):c.74G>A (p.Arg25Gln)	GDPD3 (R25Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2376380	NM_024307.3(GDPD3):c.580G>A (p.Glu194Lys)	GDPD3 (E136K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2372298	NM_024307.3(GDPD3):c.275G>A (p.Arg92His)	GDPD3 (R34H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2370851	NM_024307.3(GDPD3):c.391C>T (p.Arg131Cys)	GDPD3 (R131C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2366969	NM_024307.3(GDPD3):c.913C>T (p.Arg305Trp)	GDPD3, YPEL3-DT (R247W +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2365025	NM_024307.3(GDPD3):c.503G>A (p.Arg168His)	GDPD3 (R110H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2277706	NM_024307.3(GDPD3):c.625C>T (p.Leu209Phe)	GDPD3 (L151F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2258466	NM_024307.3(GDPD3):c.16T>C (p.Tyr6His)	GDPD3 (Y6H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2206754	NM_024307.3(GDPD3):c.511C>T (p.Arg171Cys)	GDPD3 (R113C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1810304	GRCh37/hg19 16p11.2(chr16:29670770-30207956)x3	MVP, YPEL3 +27 more	Copy number gain	Chromosome 16p11.2 duplication syndrome	Gnot provided
Select item 1810288	GRCh37/hg19 16p11.2(chr16:29651706-30193525)x1	C16orf92, CDIPT +24 more	Copy number loss	Proximal 16p11.2 microdeletion syndrome	Gnot provided
Select item 1808696	GRCh37/hg19 16p12.2-11.2(chr16:21576803-30177240)x3	ALDOA, APOBR +93 more	Copy number gain	not provided	GPathogenic
Select item 1808476	GRCh37/hg19 16p11.2(chr16:29567296-30240227)x1	ALDOA, ASPHD1 +28 more	Copy number loss	not provided	GPathogenic
Select item 1808472	GRCh37/hg19 16p11.2(chr16:29567296-30240227)x3	ALDOA, ASPHD1 +28 more	Copy number gain	not provided	GPathogenic
Select item 1808204	GRCh37/hg19 16p11.2(chr16:29432213-30240227)x1	YPEL3, ZG16 +31 more	Copy number loss	not provided	GPathogenic
Select item 1807842	GRCh37/hg19 16p11.2(chr16:29622758-30240227)x3	ALDOA, ASPHD1 +28 more	Copy number gain	not provided	GPathogenic
Select item 1807828	GRCh37/hg19 16p11.2(chr16:28466731-30321320)x1	ALDOA, APOBR +48 more	Copy number loss	not provided	GPathogenic
Select item 1807793	GRCh37/hg19 16p13.3-11.2(chr16:4380767-30445350)x3	ABAT, ABCC1 +226 more	Copy number gain	not provided	GPathogenic
Select item 1706497	GRCh37/hg19 16p11.2(chr16:29432212-30177807)x1	HIRIP3, INO80E +27 more	Copy number loss	See cases	GPathogenic
Select item 1704350	GRCh37/hg19 16p11.2(chr16:29567296-30177807)x1	ALDOA, ASPHD1 +24 more	Copy number loss	Dysmorphic features	GUncertain significance
Select item 1703603	GRCh37/hg19 16p11.2(chr16:29591078-30177240)	ALDOA, ASPHD1 +24 more	Copy number gain	Chromosome 16p11.2 duplication syndrome	GPathogenic
Select item 1703600	GRCh37/hg19 16p11.2(chr16:29628661-30306955)	ALDOA, ASPHD1 +28 more	Copy number gain	Chromosome 16p11.2 duplication syndrome	GPathogenic
Select item 1703578	GRCh37/hg19 16p11.2(chr16:29567295-30178406)	ALDOA, ASPHD1 +24 more	Copy number loss	Proximal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1703556	GRCh37/hg19 16p11.2(chr16:29580020-30177916)	ALDOA, ASPHD1 +24 more	Copy number loss	Proximal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1703545	GRCh37/hg19 16p11.2(chr16:29580020-30177999)	ALDOA, ASPHD1 +24 more	Copy number loss	Proximal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1703541	GRCh37/hg19 16p11.2(chr16:29567295-30177916)	MVP, PAGR1 +24 more	Copy number loss	Rokitansky sequence	GPathogenic
Select item 1703233	Single allele	LOC130058781, MAZ +92 more	Deletion	Chromosome 16p11.2 duplication syndrome	GPathogenic
Select item 1694809	GRCh37/hg19 16p11.2(chr16:29674300-30200008)x1	CORO1A, DOC2A +25 more	Copy number loss	not provided	GPathogenic
Select item 1684661	NC_000016.10:g.29640592_30187862del	GDPD3, LOC130058793 +101 more	Deletion	Proximal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1684552	GRCh37/hg19 16p11.2(chr16:29601322-30201321)x1	GDPD3, KCTD13 +25 more	Copy number loss	See cases	GPathogenic
Select item 1679413	NC_000016.10:g.(29449194_29595531)_(30188533_30335547)del	LOC130058767, LOC130058768 +119 more	Deletion	See cases	GLikely pathogenic, low penetrance
Select item 1339950	GRCh37/hg19 16p11.2(chr16:29567295-30320307)x1	ALDOA, ASPHD1 +28 more	Copy number loss	Chromosome 16p11.2 duplication syndrome	Gnot provided
Select item 1339949	GRCh37/hg19 16p11.2(chr16:29591078-30177240)x3	ALDOA, ASPHD1 +24 more	Copy number gain	Chromosome 16p11.2 duplication syndrome	Gnot provided
Select item 1339776	GRCh37/hg19 16p11.2(chr16:29678569-30198121)x1	ALDOA, ASPHD1 +25 more	Copy number loss	not provided	Gnot provided
Select item 1330307	GRCh37/hg19 16p11.2(chr16:29590554-30197341)x3	PPP4C, PRRT2 +25 more	Copy number gain	16p11.2 duplication syndrome	GPathogenic
Select item 1330208	GRCh37/hg19 16p11.2(chr16:29675000-30200335)x3	ALDOA, ASPHD1 +25 more	Copy number gain	Distal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1330201	GRCh37/hg19 16p11.2(chr16:29808153-30750270)x3	ALDOA, ASPHD1 +42 more	Copy number gain	Chromosome 16p11.2 duplication syndrome	GPathogenic
Select item 1330191	GRCh37/hg19 16p11.2(chr16:29675000-30200058)x3	ALDOA, ASPHD1 +25 more	Copy number gain	16p11.2p12.2 microduplication syndrome	GPathogenic
Select item 1330182	GRCh37/hg19 16p11.2(chr16:29511270-30199844)x1	ALDOA, ASPHD1 +25 more	Copy number loss	Distal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1330167	GRCh37/hg19 16p11.2(chr16:29464904-30233799)x3	ALDOA, ASPHD1 +31 more	Copy number gain	Distal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1330166	GRCh37/hg19 16p11.2(chr16:29511270-30200335)x1	ALDOA, ASPHD1 +25 more	Copy number loss	Distal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1330158	GRCh37/hg19 16p11.2(chr16:29675000-30199844)x1	ALDOA, ASPHD1 +25 more	Copy number loss	Distal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1330157	GRCh37/hg19 16p11.2(chr16:29974415-30596982)x1	ALDOA, BOLA2B +29 more	Copy number loss	Distal 16p11.2 microdeletion syndrome	GLikely pathogenic
Select item 1328112	GRCh37/hg19 16p11.2(chr16:29606372-30199622)x1	ALDOA, ASPHD1 +25 more	Copy number loss	not provided	GPathogenic
Select item 1199403	GRCh37/hg19 16p11.2(chr16:29565626-30221925)x1	YPEL3, MAZ +28 more	Copy number loss	See cases	GPathogenic
Select item 1180509	GRCh37/hg19 16p11.2(chr16:29615859-30199454)x1	ALDOA, ASPHD1 +25 more	Copy number loss	not provided	GPathogenic
Select item 1176677	GRCh37/hg19 16p11.2(chr16:29675050-30218221)x1	SEZ6L2, SLX1A +28 more	Copy number loss	not provided	GPathogenic
Select item 1176676	GRCh37/hg19 16p11.2(chr16:29675050-30200008)x1	ALDOA, ASPHD1 +25 more	Copy number loss	not provided	GPathogenic
Select item 1172563	GRCh37/hg19 16p11.2(chr16:29545794-30307472)x1	ALDOA, ASPHD1 +28 more	Copy number loss	See cases	GPathogenic
Select item 1077186	Single allele	GDPD3, ALDOA +28 more	Deletion	Proximal 16p11.2 microdeletion syndrome	GPathogenic
Select item 1075384	NC_000016.9:g.(?_29802081)_(30200285_?)del	ALDOA, ASPHD1 +21 more	Deletion	Episodic kinesigenic dyskinesia	GPathogenic
Select item 1063963	NC_000016.9:g.(?_29802081)_(30199917_?)dup	TMEM219, YPEL3 +21 more	Duplication	HNSHA due to aldolase A deficiency +2 more	GUncertain significance
Select item 1054446	NC_000016.9:g.(?_29802081)_(30199917_?)del	KIF22, MAPK3 +21 more	Deletion	Episodic kinesigenic dyskinesia	GPathogenic
Select item 1025477	NC_000016.9:g.(?_29802081)_(30200285_?)dup	KCTD13, MVP +21 more	Duplication	Episodic kinesigenic dyskinesia	GUncertain significance
Select item 997089	GRCh37/hg19 16p11.2(chr16:29673954-30198600)	C16orf92, CDIPT +25 more	Copy number gain	Autism	GPathogenic
Select item 997070	GRCh37/hg19 16p11.2(chr16:29652999-30198600)	ALDOA, ASPHD1 +25 more	Copy number loss	Abnormal fetal cardiovascular morphology	GPathogenic
Select item 997050	GRCh37/hg19 16p11.2(chr16:29652999-30197341)	HIRIP3, INO80E +25 more	Copy number gain	Severe sensorineural hearing impairment +2 more	GPathogenic
Select item 992652	GRCh37/hg19 16p11.2(chr16:29443322-30320321)x3	MAPK3, SLX1A +31 more	Copy number gain	not provided	GPathogenic
Select item 983281	GRCh37/hg19 16p13.3-11.2(chr16:2959279-30190593)x3	ABAT, ABCC1 +252 more	Copy number gain	See cases	GPathogenic
Select item 983192	GRCh37/hg19 16p11.2(chr16:29592797-30190593)x3	DOC2A, MVP +24 more	Copy number gain	See cases	GPathogenic
Select item 983165	GRCh37/hg19 16p11.2(chr16:29448001-30302100)	KIF22, TBX6 +31 more	Copy number gain	See cases	GPathogenic
Select item 979441	GRCh37/hg19 16p11.2(chr16:29383808-30177240)x3	MAZ, SLX1B +27 more	Copy number gain	not provided	GPathogenic
Select item 979440	GRCh37/hg19 16p11.2(chr16:28488319-30178406)x1	ATXN2L, PAGR1 +44 more	Copy number loss	not provided	GPathogenic
Select item 974579	Single allele	DOC2A, GDPD3 +31 more	Deletion	Proximal 16p11.2 microdeletion syndrome	Grisk factor
Select item 929398	GRCh37/hg19 16p11.2(chr16:29595483-30215621)x1	ALDOA, ASPHD1 +28 more	Copy number loss	See cases	GPathogenic
Select item 815818	GRCh37/hg19 16p11.2(chr16:29432212-30178406)x1	CDIPT, DOC2A +27 more	Copy number loss	not provided	GPathogenic
Select item 815817	GRCh37/hg19 16p11.2(chr16:29432212-30177240)x1	SULT1A4, KIF22 +27 more	Copy number loss	not provided	GPathogenic
Select item 815815	GRCh37/hg19 16p11.2(chr16:28466730-30178406)x1	ZG16, QPRT +44 more	Copy number loss	not provided	GPathogenic
Select item 813717	GRCh37/hg19 16p13.3-11.2(chr16:5805001-34230001)	ABAT, ABCC1 +250 more	Copy number gain	Microcephaly	GPathogenic

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