dbVar for Gene (Select 119437) - 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
nsv7148086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 124,895,517-135,440,296 , GRCh38.p12 chr10: 123,136,001-133,626,792	FANK1, LOC105378534, 159 more genes
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
nsv7060863	inversion	1	nstd229	human		GRCh38 chr10: 127,697,992-132,467,329 , GRCh37.p13 chr10: 129,496,256-134,280,833	EBF3-AS1, GLRX3, 47 more genes
nsv6893691	copy number variation	1	nstd229	human		GRCh38 chr10: 129,843,967-130,644,647 , GRCh37.p13 chr10: 131,642,231-132,442,911	EBF3, LOC105378561, 7 more genes
nsv6891951	copy number variation	1	nstd229	human		GRCh38 chr10: 130,086,301-130,120,900 , GRCh37.p13 chr10: 131,884,565-131,919,164	LOC102724883, C10orf143, 1 more genes
nsv6888209	copy number variation	1	nstd229	human		GRCh38 chr10: 130,100,001-130,118,000 , GRCh37.p13 chr10: 131,898,265-131,916,264	C10orf143, LOC102724883, 1 more genes
nsv6885479	copy number variation	1	nstd229	human		GRCh38 chr10: 129,920,201-130,157,600 , GRCh37.p13 chr10: 131,718,465-131,955,864	CTAGE7P, LOC102724883, 4 more genes
nsv6883379	copy number variation	1	nstd229	human		GRCh38 chr10: 130,001,001-130,157,600 , GRCh37.p13 chr10: 131,799,265-131,955,864	LOC105378561, GLRX3, 3 more genes
nsv6637456	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 126,662,496-133,985,966 , GRCh38.p12 chr10: 124,973,927-132,172,462	LOC107984186, LOC105378550, 82 more genes
nsv6637243	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 130,043,370-135,345,340 , GRCh38.p12 chr10: 128,245,106-133,531,836	DPYSL4, LINC02667, 79 more genes
nsv6634415	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 126,914,469-135,427,143 , GRCh38.p12 chr10: 125,225,900-133,613,639	MGMT, LINC01168, 127 more genes
nsv6634408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 127,198,625-135,427,143 , GRCh38.p12 chr10: 125,510,056-133,613,639	MIR202HG, LOC105378563, 123 more genes
nsv6450947	copy number variation	1	nstd223	human		GRCh38 chr10: 130,086,363-130,120,911 , GRCh37.p13 chr10: 131,884,627-131,919,175	CTAGE7P, LOC102724883, 1 more genes
nsv6315498	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 129,605,105-135,427,143 , GRCh38.p12 chr10: 127,806,841-133,613,639	LINC02646, GLRX3, 87 more genes
nsv6314191	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 131,324,081-132,362,298 , GRCh38.p12 chr10: 129,525,817-130,564,034	LINC02666, LOC105378561, 12 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
nsv6314079	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 129,914,228-135,427,143 , GRCh38.p12 chr10: 128,115,964-133,613,639	UTF1, RPL5P28, 83 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 219

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Number of Variants: 20

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