dbVar for Gene (Select 26355) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7148201	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857	NECTIN3, H2BP3, 418 more genes
nsv7144758	insertion	1	nstd232	human		GRCh37.p13 chr3: 122,103,147-122,103,147 , GRCh38.p12 chr3: 122,384,300-122,384,300	FAM162A
nsv7137461	insertion	1	nstd232	human		GRCh37.p13 chr3: 122,123,215-122,123,215 , GRCh38.p12 chr3: 122,404,368-122,404,368	FAM162A
nsv7096531	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 121,489,192-125,313,644 , GRCh38.p12 chr3: 121,770,345-125,594,800	MEMO1P6, HACD2, 62 more genes
nsv6712243	copy number variation	1	nstd229	human		GRCh38 chr3: 122,388,274-122,393,248 , GRCh37.p13 chr3: 122,107,121-122,112,095	FAM162A
nsv6708723	copy number variation	1	nstd229	human		GRCh38 chr3: 122,399,707-122,402,788 , GRCh37.p13 chr3: 122,118,554-122,121,635	FAM162A
nsv6707907	copy number variation	1	nstd229	human		GRCh38 chr3: 113,856,250-122,791,940 , GRCh37.p13 chr3: 113,575,097-122,510,787	COX17, LOC105374052, 133 more genes
nsv6707470	copy number variation	1	nstd229	human		GRCh38 chr3: 122,399,101-122,630,700 , GRCh37.p13 chr3: 122,117,948-122,349,547	WDR5B, WDR5B-DT, 8 more genes
nsv6703931	copy number variation	1	nstd229	human		GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124	RPS24P9, LOC105374064, 149 more genes
nsv6699259	copy number variation	1	nstd229	human		GRCh38 chr3: 122,386,523-122,394,381 , GRCh37.p13 chr3: 122,105,370-122,113,228	FAM162A
nsv6698407	copy number variation	1	nstd229	human		GRCh38 chr3: 122,157,201-122,395,100 , GRCh37.p13 chr3: 121,876,048-122,113,947	CSTA, MIX23, 3 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	H1-10, AADACL2-AS1, 846 more genes
nsv6370959	copy number variation	1	nstd223	human		GRCh38 chr3: 122,381,201-122,389,000 , GRCh37.p13 chr3: 122,100,048-122,107,847	MIX23, FAM162A
nsv6315285	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr3: 122,157,406-123,113,479 , GRCh37.p13 chr3: 121,876,253-122,832,326	SEMA5B, EIF4BP8, 19 more genes
nsv6311770	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203	HNRNPA1P23, MIX23, 278 more genes
nsv6299167	copy number variation	1	nstd186	human		GRCh37 chr3: 122,107,117-122,112,094 , GRCh38.p12 chr3: 122,388,270-122,393,247	FAM162A
nsv6134575	copy number variation	1	nstd213	human		GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157	ACP3, ADCY5, 308 more genes
nsv6112688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144	RNU4-62P, MTCO1P29, 169 more genes
nsv5973212	inversion	1	nstd209	human		GRCh38 chr3: 121,858,185-122,522,926 , GRCh37.p13 chr3: 121,577,032-122,241,773	CASR, CD86, 12 more genes
nsv5889621	copy number variation	1	nstd209	human		GRCh38 chr3: 122,394,282-122,394,520 , GRCh37.p13 chr3: 122,113,129-122,113,367	FAM162A

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Items: 1 to 20 of 144

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Number of Variants: 20

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