dbVar for Gene (Select 100506126) - 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
nsv6892830	copy number variation	1	nstd229	human		GRCh38 chr10: 117,664,803-118,402,207 , GRCh37.p13 chr10: 119,424,314-120,161,719	RAB11FIP2, FAM204A, 6 more genes
nsv6885821	copy number variation	1	nstd229	human		GRCh38 chr10: 118,355,386-118,357,123 , GRCh37.p13 chr10: 120,114,898-120,116,635	LINC00867
nsv6620317	copy number variation	1	nstd224	human		GRCh37 chr10: 119,424,467-120,159,880 , GRCh38.p12 chr10: 117,664,956-118,400,368	RAB11FIP2, FAM204A, 6 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
nsv6290269	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 118,891,670-122,349,064 , GRCh38.p12 chr10: 117,132,159-120,589,552	MCMBP, PDZD8, 54 more genes
nsv6131937	copy number variation	1	nstd213	human		GRCh37 chr10: 119,240,000-120,730,001 , GRCh38.p12 chr10: 117,480,489-118,970,489	EMX2, PRLHR, 16 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
nsv5974801	inversion	1	nstd209	human		GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953	EMX2, PRLHR, 48 more genes
nsv5672603	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789	ACADSB, DMBT1, 84 more genes
nsv5507095	copy number variation	1	nstd206	human		GRCh38 chr10: 118,358,530-118,358,600 , GRCh37.p13 chr10: 120,118,042-120,118,112	LINC00867
nsv5500799	copy number variation	1	nstd206	human		GRCh38 chr10: 118,346,368-118,602,368 , GRCh37.p13 chr10: 120,105,880-120,361,880	PRLHR, SLC25A18P1, 2 more genes
nsv5354502	translocation	1	nstd200	human		GRCh38 chr10: 118,358,461-118,358,461 , GRCh38 chr10: 118,358,518-118,358,518 , GRCh37.p13 chr10: 120,117,973-120,117,973 , GRCh37.p13 chr10: 120,118,030-120,118,030	LINC00867
nsv4675991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639	STK32C, LOC105378542, 237 more genes
nsv4456626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639	LOC105378521, ZRANB1, 317 more genes
nsv4349508	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 117,024,753-124,942,806 , GRCh38.p12 chr10: 115,265,276-123,183,290	PRLHR, LOC105378513, 121 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 96

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Number of Variants: 20

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