ClinVar for Gene (Select 6003) - ClinVar

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Links from Gene

Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3153828	NM_002927.5(RGS13):c.47C>A (p.Ser16Tyr)	RGS13 (S16Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153827	NM_002927.5(RGS13):c.302T>C (p.Ile101Thr)	RGS13 (I101T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153826	NM_002927.5(RGS13):c.192G>T (p.Trp64Cys)	RGS13 (W64C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529521	NM_002927.5(RGS13):c.451A>G (p.Lys151Glu)	RGS13 (K151E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512233	NM_002927.5(RGS13):c.436T>C (p.Tyr146His)	RGS13 (Y146H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461556	NM_002927.5(RGS13):c.311C>T (p.Ser104Leu)	RGS13 (S104L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460762	NM_002927.5(RGS13):c.8G>A (p.Arg3Lys)	RGS13 (R3K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412329	NM_002927.5(RGS13):c.389T>C (p.Met130Thr)	RGS13 (M130T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373716	NM_002927.5(RGS13):c.58C>T (p.Pro20Ser)	RGS13 (P20S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335386	NM_002927.5(RGS13):c.10C>T (p.Arg4Trp)	RGS13 (R4W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809264	GRCh37/hg19 1q25.3-32.3(chr1:181453460-213107248)x3	IGFN1, IKBKE +211 more	Copy number gain	not provided	GPathogenic
Select item 1807694	GRCh37/hg19 1q31.1-32.1(chr1:189633885-199854163)x1	ASPM, ATP6V1G3 +28 more	Copy number loss	not provided	GLikely pathogenic
Select item 1527448	GRCh37/hg19 1q25.2-32.1(chr1:179413479-201764737)	ACBD6, APOBEC4 +98 more	Copy number loss	not specified	GPathogenic
Select item 1527437	GRCh37/hg19 1q25.2-32.1(chr1:179073386-200192265)	ABL2, ACBD6 +82 more	Copy number loss	not specified	GPathogenic
Select item 1527404	GRCh37/hg19 1q24.3-31.3(chr1:171990029-195086758)	BRINP2, BRINP3 +101 more	Copy number loss	not specified	GPathogenic
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	KLHL12, LNCATV +956 more	Duplication	Paragangliomas 3 +2 more	GUncertain significance
Select item 814145	GRCh37/hg19 1q25.2-32.1(chr1:177551193-199599056)x1	ABL2, ACBD6 +88 more	Copy number loss	not provided	GPathogenic
Select item 685144	GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3	CAPN9, CATSPERE +433 more	Copy number gain	not provided	GPathogenic
Select item 560081	Single allele	B3GALT2, CDC73 +53 more	Deletion	Parathyroid carcinoma +2 more	GPathogenic
Select item 442387	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	PADI1, PADI2 +2014 more	Copy number gain	See cases	GPathogenic
Select item 442386	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	NID1, NIPAL3 +2014 more	Copy number gain	See cases	GPathogenic
Select item 442042	GRCh37/hg19 1q25.2-32.1(chr1:179011314-199022759)x1	NIBAN1, NMNAT2 +83 more	Copy number loss	See cases	GPathogenic
Select item 146285	GRCh38/hg38 1q31.1-32.1(chr1:189034483-199615866)x1	ASPM, ATP6V1G3 +173 more	Copy number loss	See cases	GPathogenic
Select item 144717	GRCh38/hg38 1q25.2-31.3(chr1:176595962-196301688)x1	LOC126805952, LOC126805953 +455 more	Copy number loss	See cases	GPathogenic
Select item 60078	GRCh38/hg38 1q31.2(chr1:192567876-193180049)x1	B3GALT2, CDC73 +21 more	Copy number loss	See cases	GPathogenic
Select item 60076	GRCh38/hg38 1q25.2-32.1(chr1:179032905-199724897)x1	LOC129388668, LOC129388669 +477 more	Copy number loss	See cases	GPathogenic
Select item 58112	GRCh38/hg38 1q31.1-42.11(chr1:187143981-224299417)x3	LOC129932244, LOC129932245 +1147 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 27