dbVar for Gene (Select 399815) - 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
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
nsv5980446	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718	LINC02641, CFAP46, 194 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
nsv5512526	copy number variation	1	nstd206	human		GRCh38 chr10: 122,878,779-122,878,865 , GRCh37.p13 chr10: 124,638,295-124,638,381	FAM24B, C10orf88B, 1 more genes
nsv5500267	copy number variation	1	nstd206	human		GRCh38 chr10: 122,863,033-122,904,137 , GRCh37.p13 chr10: 124,622,549-124,663,653	FAM24B, C10orf88B, 1 more genes
nsv4977325	copy number variation	1	nstd200	human		GRCh38 chr10: 122,890,578-122,892,502 , GRCh37.p13 chr10: 124,650,094-124,652,018	C10orf88B
nsv4848228	copy number variation	1	nstd200	human		GRCh37 chr10: 124,650,094-124,652,018 , GRCh38.p12 chr10: 122,890,578-122,892,502	C10orf88B
nsv4679699	copy number variation	1	nstd189	human		GRCh37.p13 chr10: 124,478,359-125,318,025 , GRCh38.p12 chr10: 122,718,843-123,558,509	ACADSB, HMX2, 15 more genes
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
nsv4675857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 123,232,922-124,638,514 , GRCh38.p12 chr10: 121,473,408-122,878,998	LOC105378525, HTRA1, 20 more genes
nsv4609738	copy number variation	1	nstd183	human		GRCh37 chr10: 124,654,073-124,654,197 , GRCh38.p12 chr10: 122,894,557-122,894,681	C10orf88B
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
nsv4208989	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 123,721,898-126,209,916 , GRCh38.p12 chr10: 121,962,383-124,521,347	, CHST15, 44 more genes
nsv4205050	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 124,638,295-124,638,381 , GRCh38.p12 chr10: 122,878,779-122,878,865	FAM24B, C10orf88B, 1 more genes
nsv3924720	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 119,707,856-133,613,639 , GRCh37 chr10: 121,467,368-135,427,143 , NCBI36 chr10: 121,457,358-135,277,133	OR6L2P, RPL19P16, 208 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
nsv3922547	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 124,576,249-128,409,507 , GRCh37 chr10: 124,586,259-128,419,517 , GRCh38 chr10: 122,826,743-126,730,948	FAM53B, LOC107984184, 70 more genes

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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 139

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Number of Variants: 20

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