dbVar for Gene (Select 399814) - 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
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	EXOC6, VCL, 1906 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	RNU7-12P, RNU1-65P, 1876 more genes
nsv7137208	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 123,477,898-135,427,143 , GRCh38.p12 chr10: 121,718,384-133,613,639	ZRANB1, LOC105378544, 182 more genes
nsv7098893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306	LOC105378571, DOCK1, 196 more genes
nsv7093623	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 123,239,371-124,813,281 , GRCh38.p12 chr10: 121,479,857-123,053,765	TACC2, BTBD16, 25 more genes
nsv7068192	inversion	1	nstd229	human		GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347	CTBP2, RPS26P39, 114 more genes
nsv6892887	copy number variation	1	nstd229	human		GRCh38 chr10: 122,696,101-122,830,400 , GRCh37.p13 chr10: 124,455,617-124,589,916	C10orf120, FAM24B-CUZD1, 2 more genes
nsv6892577	copy number variation	1	nstd229	human		GRCh38 chr10: 121,685,649-124,297,191 , GRCh37.p13 chr10: 123,445,163-125,985,760	LOC107984128, ATE1-AS1, 39 more genes
nsv6891715	copy number variation	1	nstd229	human		GRCh38 chr10: 122,663,022-122,718,677 , GRCh37.p13 chr10: 124,422,538-124,478,193	SPADH, C10orf120
nsv6888118	copy number variation	1	nstd229	human		GRCh38 chr10: 122,696,048-122,830,392 , GRCh37.p13 chr10: 124,455,564-124,589,908	DMBT1L1, C10orf120, 2 more genes
nsv6884703	copy number variation	1	nstd229	human		GRCh38 chr10: 121,934,615-128,427,106 , GRCh37.p13 chr10: 123,694,130-130,225,370	OAT, C10orf88, 98 more genes
nsv6884641	copy number variation	1	nstd229	human		GRCh38 chr10: 122,675,962-122,845,684 , GRCh37.p13 chr10: 124,435,478-124,605,200	C10orf120, FAM24B-CUZD1, 3 more genes
nsv6638052	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 124,252,660-125,447,562 , GRCh38.p12 chr10: 122,493,144-123,688,046	C10orf88B, IKZF5, 20 more genes
nsv6637491	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 123,964,214-124,477,580 , GRCh38.p12 chr10: 122,204,699-122,718,064	TACC2, PLEKHA1, 9 more genes
nsv6585886	inversion	1	nstd223	human		GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347	LOC105378520, SPADH, 114 more genes
nsv6314129	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550	PDZD8, MIR3663HG, 122 more genes
nsv6314085	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639	LOC107984268, DPYSL4, 379 more genes
nsv6131932	copy number variation	1	nstd213	human		GRCh37 chr10: 115,960,000-125,870,001 , GRCh38.p12 chr10: 114,200,241-124,109,956	ACADSB, DMBT1, 148 more genes
nsv6131766	copy number variation	1	nstd213	human		GRCh37 chr10: 116,010,000-125,870,001 , GRCh38.p12 chr10: 114,250,241-124,109,956	ACADSB, DMBT1, 146 more genes
nsv6112765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815	STK32C, LOC105378542, 266 more genes

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Organism

Variant Type

Method Type

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 156

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Number of Variants: 20

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