FRG2[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58042	GRCh38/hg38 4q26-35.2(chr4:118065569-190042639)x3	LOC123493236, LOC123493237 +1310 more	Copy number gain	See cases	GPathogenic
Select item 58043	GRCh38/hg38 4q27-35.2(chr4:121518223-190062270)x3	LOC132089056, LOC132089057 +1245 more	Copy number gain	See cases	GPathogenic
Select item 148653	GRCh38/hg38 4q28.3-35.2(chr4:131985253-190095391)x3	LOC129993256, LOC129993257 +1068 more	Copy number gain	See cases	GPathogenic
Select item 155492	GRCh38/hg38 4q28.3-35.2(chr4:134935616-190036318)x3	NDUFC1, NEIL3 +1051 more	Copy number gain	See cases	GPathogenic
Select item 152441	GRCh38/hg38 4q32.1-35.2(chr4:160757699-190091407)x3	AADAT, ACSL1 +553 more	Copy number gain	See cases	GPathogenic
Select item 148458	GRCh38/hg38 4q32.3-35.2(chr4:166317587-190095391)x1	LOC129993480, LOC129993481 +466 more	Copy number loss	See cases	GPathogenic
Select item 153653	GRCh38/hg38 4q32.3-35.2(chr4:167373716-190036318)x1	LOC129993505, LOC129993506 +455 more	Copy number loss	See cases	GPathogenic
Select item 155264	GRCh38/hg38 4q32.3-35.2(chr4:168119317-190095391)x3	AADAT, ACSL1 +451 more	Copy number gain	See cases	GPathogenic
Select item 149543	GRCh38/hg38 4q33-35.2(chr4:169901205-190095391)x3	AADAT, ACSL1 +401 more	Copy number gain	See cases	GUncertain significance
Select item 155165	GRCh38/hg38 4q33-35.2(chr4:170899124-190036318)x1	LINC02500, LINC02504 +383 more	Copy number loss	See cases	GPathogenic
Select item 155012	GRCh38/hg38 4q34.1-35.2(chr4:172501374-190095332)x1	FAM149A, FAT1 +372 more	Copy number loss	See cases	GPathogenic
Select item 59532	GRCh38/hg38 4q34.3-35.2(chr4:177442769-190042639)x1	LOC129993464, LOC129993465 +293 more	Copy number loss	See cases	GPathogenic
Select item 148268	GRCh38/hg38 4q34.3-35.2(chr4:178014570-190095391)x1	LOC129993443, LOC129993444 +287 more	Copy number loss	See cases	GPathogenic
Select item 148187	GRCh38/hg38 4q34.3-35.2(chr4:178549472-190095391)x1	LOC126807246, LOC126807247 +286 more	Copy number loss	See cases	GPathogenic
Select item 151757	GRCh38/hg38 4q34.3-35.2(chr4:179295511-190036318)x3	ACSL1, ANKRD37 +282 more	Copy number gain	See cases	GPathogenic
Select item 146393	GRCh38/hg38 4q34.3-35.2(chr4:180451652-190095391)x3	ACSL1, ANKRD37 +275 more	Copy number gain	See cases	GLikely pathogenic
Select item 148270	GRCh38/hg38 4q34.3-35.2(chr4:180574962-190095391)x1	LOC129993452, LOC129993453 +275 more	Copy number loss	See cases	GPathogenic
Select item 154943	GRCh38/hg38 4q34.3-35.2(chr4:180717850-190095391)x3	ACSL1, ANKRD37 +274 more	Copy number gain	See cases	GPathogenic
Select item 149694	GRCh38/hg38 4q35.1-35.2(chr4:183072743-190095391)x1	ACSL1, ANKRD37 +241 more	Copy number loss	See cases	GPathogenic
Select item 59536	GRCh38/hg38 4q35.1-35.2(chr4:183354112-190042639)x1	ACSL1, ANKRD37 +228 more	Copy number loss	See cases	GPathogenic
Select item 148762	GRCh38/hg38 4q35.1-35.2(chr4:186129390-190095391)x1	CYP4V2, DBET +72 more	Copy number loss	See cases	GUncertain significance
Select item 1703259	Single allele	DBET, DUX4 +67 more	Deletion	Hereditary factor XI deficiency disease	GLikely pathogenic
Select item 60220	GRCh38/hg38 4q35.2(chr4:187347785-190042639)x1	FRG1, FRG1-DT +42 more	Copy number loss	See cases	GUncertain significance
Select item 57916	GRCh38/hg38 4q35.2(chr4:188165012-190042639)x3	FRG1, FRG1-DT +25 more	Copy number gain	See cases	GUncertain significance
Select item 148378	GRCh38/hg38 4q35.2(chr4:188957851-190095391)x1	DBET, FRG1 +14 more	Copy number loss	See cases	GLikely benign
Select item 150025	GRCh38/hg38 4q35.2(chr4:189047095-190095391)x3	DBET, FRG1 +14 more	Copy number gain	See cases	GUncertain significance
Select item 153599	GRCh38/hg38 4q35.2(chr4:189102173-190036318)x1	FRG1, FRG1-DT +12 more	Copy number loss	See cases	GLikely benign
Select item 154240	GRCh38/hg38 4q35.2(chr4:189102550-190036318)x1	LOC123493255, LOC126088085 +12 more	Copy number loss	See cases	GUncertain significance
Select item 150844	GRCh38/hg38 4q35.2(chr4:189106871-190095391)x1	DBET, FRG1 +13 more	Copy number loss	See cases	GLikely benign
Select item 153448	GRCh38/hg38 4q35.2(chr4:189328689-190036318)x3	FRG1, FRG1-DT +10 more	Copy number gain	See cases	GUncertain significance
Select item 149327	GRCh38/hg38 4q35.2(chr4:189476888-190095391)x1	DBET, FRG1 +11 more	Copy number loss	See cases	GLikely benign
Select item 155542	GRCh38/hg38 4q35.2(chr4:189513541-190036318)x3	FRG1, FRG1-DT +10 more	Copy number gain	See cases	GUncertain significance
Select item 153176	GRCh38/hg38 4q35.2(chr4:189588653-190036318)	FRG1, FRG1-DT +9 more	Copy number loss	See cases	GPathogenic
Select item 145261	GRCh38/hg38 4q35.2(chr4:190022219-190091407)x3	DBET, FRG2	Copy number gain	See cases	GBenign
Select item 2263573	NM_001286820.2(FRG2):c.770G>C (p.Arg257Thr)	FRG2 (R256T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2350030	NM_001286820.2(FRG2):c.731C>T (p.Pro244Leu)	FRG2 (P243L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2486838	NM_001286820.2(FRG2):c.695C>A (p.Ala232Glu)	FRG2 (A232E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2484643	NM_001286820.2(FRG2):c.695C>T (p.Ala232Val)	FRG2 (A231V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2220367	NM_001286820.2(FRG2):c.669G>T (p.Gln223His)	FRG2 (Q223H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2381629	NM_001286820.2(FRG2):c.643C>T (p.Arg215Trp)	FRG2 (R214W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2318737	NM_001286820.2(FRG2):c.638G>A (p.Arg213Gln)	FRG2 (R212Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2379231	NM_001286820.2(FRG2):c.637C>T (p.Arg213Trp)	FRG2 (R213W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2299330	NM_001286820.2(FRG2):c.621G>T (p.Gln207His)	FRG2 (Q206H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2484750	NM_001286820.2(FRG2):c.547A>G (p.Met183Val)	FRG2 (M182V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2371546	NM_001286820.2(FRG2):c.509C>T (p.Pro170Leu)	FRG2 (P169L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351011	NM_001286820.2(FRG2):c.487C>T (p.Arg163Trp)	FRG2 (R162W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232176	NM_001286820.2(FRG2):c.476G>A (p.Arg159Gln)	FRG2 (R159Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2344073	NM_001286820.2(FRG2):c.449C>T (p.Ser150Phe)	FRG2 (S150F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2530054	NM_001286820.2(FRG2):c.445C>T (p.His149Tyr)	FRG2 (H148Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2270450	NM_001286820.2(FRG2):c.278G>A (p.Arg93Gln)	FRG2 (R92Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2295423	NM_001286820.2(FRG2):c.161A>C (p.Lys54Thr)	FRG2 (K54T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2226207	NM_001286820.2(FRG2):c.14A>C (p.Asn5Thr)	FRG2 (N5T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3062804	GRCh37/hg19 4q27-35.2(chr4:123399154-190957473)x3	FAM149A, FAM218A +197 more	Copy number gain	not specified	GPathogenic
Select item 3062803	GRCh37/hg19 4q32.1-35.2(chr4:161589441-190957473)x1	AADAT, ACSL1 +85 more	Copy number loss	not specified	GPathogenic
Select item 3062767	GRCh37/hg19 4q24-35.2(chr4:101203509-190957473)x3	AADAT, ABCE1 +286 more	Copy number gain	not specified	GPathogenic
Select item 3024634	GRCh37/hg19 4q32.3-35.2(chr4:169060637-191154276)x1	AADAT, ACSL1 +68 more	Copy number loss	not provided	GPathogenic
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	TMA16, CXCL1 +537 more	Copy number gain	not provided	GPathogenic
Select item 2685138	GRCh37/hg19 4q35.1-35.2(chr4:187040986-190957473)x1	CYP4V2, F11 +9 more	Copy number loss	not provided	GUncertain significance
Select item 2684399	GRCh37/hg19 4q32.3-35.2(chr4:167409608-190957473)x3	AADAT, ACSL1 +69 more	Copy number gain	not provided	GPathogenic
Select item 2583028	GRCh37/hg19 4q35.2(chr4:188923962-190948359)x1	FRG1, FRG2 +3 more	Copy number loss	not provided	GUncertain significance
Select item 1808963	GRCh37/hg19 4q35.2(chr4:187853428-190957473)x3	FRG1, FRG2 +3 more	Copy number gain	not provided	GUncertain significance
Select item 1807820	GRCh37/hg19 4q35.1-35.2(chr4:183694501-190957473)x1	ACSL1, ANKRD37 +37 more	Copy number loss	not provided	GPathogenic
Select item 1711166	GRCh37/hg19 4q32.3-35.2(chr4:167779888-190957473)x1	AADAT, ACSL1 +69 more	Copy number loss	See cases	GPathogenic
Select item 1711100	GRCh37/hg19 4q32.1-35.2(chr4:159174483-190957473)x1	AADAT, ACSL1 +93 more	Copy number loss	See cases	GPathogenic
Select item 1710924	GRCh37/hg19 4q35.1-35.2(chr4:185211271-190957473)x1	ACSL1, ANKRD37 +26 more	Copy number loss	See cases	GPathogenic
Select item 1704649	GRCh37/hg19 4q34.1-35.2(chr4:174944132-190957473)x1	ACSL1, ADAM29 +50 more	Copy number loss	FETAL DEMISE	GPathogenic
Select item 1527143	GRCh37/hg19 4q35.1-35.2(chr4:185381293-190957473)	CFAP96, ANKRD37 +26 more	Copy number loss	not specified	GPathogenic
Select item 1527141	GRCh37/hg19 4q35.1-35.2(chr4:183221828-190957473)	ACSL1, ANKRD37 +37 more	Copy number loss	not specified	GPathogenic
Select item 1527139	GRCh37/hg19 4q34.1-35.2(chr4:175855408-190957473)	ACSL1, ADAM29 +46 more	Copy number gain	not specified	GPathogenic
Select item 1340954	GRCh37/hg19 4q35.2(chr4:189828191-190957473)x1	FRG1, FRG2	Copy number loss	not provided	GUncertain significance
Select item 1340519	GRCh37/hg19 4q35.2(chr4:189351336-190957473)x1	FRG1, FRG2	Copy number loss	not provided	GUncertain significance
Select item 979496	GRCh37/hg19 4q35.2(chr4:187391214-190957473)x1	ZFP42, FAT1 +5 more	Copy number loss	not provided	GPathogenic
Select item 814636	GRCh37/hg19 4q34.3-35.2(chr4:178566256-190957473)x1	ACSL1, ANKRD37 +37 more	Copy number loss	not provided	GPathogenic
Select item 814622	GRCh37/hg19 4q32.3-35.2(chr4:165010461-190957473)x1	AADAT, ACSL1 +79 more	Copy number loss	not provided	GPathogenic
Select item 809725	GRCh37/hg19 4q35.1-35.2(chr4:183245174-190948359)x1	ACSL1, ANKRD37 +37 more	Copy number loss	not provided	GLikely pathogenic
Select item 689174	GRCh37/hg19 4q34.3-35.2(chr4:179996712-190957473)x1	ACSL1, ANKRD37 +37 more	Copy number loss	not provided	GPathogenic
Select item 688798	GRCh37/hg19 4q35.2(chr4:190023312-190957473)x1	FRG1, FRG2	Copy number loss	not provided	GUncertain significance
Select item 688407	GRCh37/hg19 4q31.3-35.2(chr4:151174061-190957473)x3	AADAT, ACSL1 +131 more	Copy number gain	not provided	GPathogenic
Select item 687025	GRCh37/hg19 4q35.2(chr4:190021956-190957473)x1	FRG1, FRG2	Copy number loss	not provided	GUncertain significance
Select item 686652	GRCh37/hg19 4q32.3-35.2(chr4:169607746-190957473)x3	AGA, ANKRD37 +65 more	Copy number gain	not provided	GPathogenic
Select item 685477	GRCh37/hg19 4q35.1-35.2(chr4:184648532-190957473)x1	FAT1, FRG1 +28 more	Copy number loss	not provided	GPathogenic
Select item 685186	GRCh37/hg19 4q35.2(chr4:189779845-190957473)x1	FRG1, FRG2	Copy number loss	not provided	GUncertain significance
Select item 685118	GRCh37/hg19 4q35.2(chr4:189632857-190957473)x1	FRG1, FRG2	Copy number loss	not provided	GUncertain significance
Select item 685014	GRCh37/hg19 4q32.3-35.2(chr4:166623890-190957473)x1	AADAT, ACSL1 +70 more	Copy number loss	not provided	GPathogenic
Select item 635958	Single allele	FRG1, FRG2	Duplication	Neurodevelopmental disorder	GPathogenic
Select item 563018	GRCh37/hg19 4q35.2(chr4:190023704-190957473)x1	FRG1, FRG2	Copy number loss	not provided	GUncertain significance
Select item 563016	GRCh37/hg19 4q35.2(chr4:188478516-190957473)x1	TRIML2, FRG2 +3 more	Copy number loss	not provided	GPathogenic
Select item 563008	GRCh37/hg19 4q35.1-35.2(chr4:185017749-190957473)x3	ACSL1, ANKRD37 +27 more	Copy number gain	not provided	GPathogenic
Select item 563006	GRCh37/hg19 4q34.3-35.2(chr4:178771936-190957473)x3	ACSL1, ANKRD37 +37 more	Copy number gain	not provided	GPathogenic
Select item 563004	GRCh37/hg19 4q34.2-35.2(chr4:176493246-190957473)x1	ACSL1, AGA +45 more	Copy number loss	not provided	GPathogenic
Select item 563003	GRCh37/hg19 4q34.1-35.2(chr4:175709188-190957473)x1	ACSL1, ADAM29 +47 more	Copy number loss	not provided	GPathogenic
Select item 562995	GRCh37/hg19 4q32.3-35.2(chr4:169969014-190957473)x1	AADAT, ACSL1 +63 more	Copy number loss	not provided	GPathogenic
Select item 562989	GRCh37/hg19 4q32.1-35.2(chr4:159492464-190957473)x3	CFAP96, CFAP97 +92 more	Copy number gain	not provided	GPathogenic
Select item 446364	GRCh37/hg19 4q35.2(chr4:190028469-190963766)x1	FRG1, FRG2	Copy number loss	See cases	GUncertain significance
Select item 443800	GRCh37/hg19 4q32.1-35.2(chr4:156465633-190957473)x3	AADAT, ACSL1 +102 more	Copy number gain	See cases	GPathogenic
Select item 443483	GRCh37/hg19 4q22.1-35.2(chr4:93071152-190957473)x3	AADAT, ABCE1 +314 more	Copy number gain	See cases	GPathogenic
Select item 443385	GRCh37/hg19 4q32.3-35.2(chr4:166436844-190957473)x3	AADAT, ACSL1 +70 more	Copy number gain	See cases	GPathogenic
Select item 443369	GRCh37/hg19 4q34.2-35.2(chr4:176306103-190957473)x3	ACSL1, AGA +45 more	Copy number gain	See cases	GPathogenic
Select item 443064	GRCh37/hg19 4q35.1-35.2(chr4:184852835-190957473)x1	ACSL1, ANKRD37 +28 more	Copy number loss	See cases	GLikely pathogenic
Select item 442869	GRCh37/hg19 4q34.3-35.2(chr4:180702769-190957473)x3	CENPU, ACSL1 +37 more	Copy number gain	See cases	GPathogenic

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