dbVar for Gene (Select 2018) - 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
nsv6443595	copy number variation	1	nstd223	human		GRCh38 chr10: 117,535,309-117,887,959 , GRCh37.p13 chr10: 119,294,820-119,647,470	LINC02674, EMX2, 2 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
nsv4977133	copy number variation	1	nstd200	human		GRCh38 chr10: 117,547,836-117,547,941 , GRCh37.p13 chr10: 119,307,347-119,307,452	EMX2
nsv4974087	copy number variation	1	nstd200	human		GRCh38 chr10: 117,535,309-117,887,959 , GRCh37.p13 chr10: 119,294,820-119,647,470	LINC02674, LOC107984274, 2 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
nsv4348764	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591	LOC105378492, VENTX, 373 more genes
nsv4342336	sequence alteration	1	nstd166	human		GRCh37.p13 chr10: 118,638,442-121,163,255 , GRCh38.p12 chr10: 116,878,931-119,403,743	EIF3A, VAX1, 38 more genes
nsv3923859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674	AS-PTPRE, SFXN4, 330 more genes
nsv3923769	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291	LOC105378493, LINC02627, 477 more genes

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 124

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Number of Variants: 20

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