dbVar for Gene (Select 145946) - 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
nsv6112780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538	LOC105371009, ST8SIA2, 149 more genes
nsv5531067	copy number variation	1	nstd206	human		GRCh38 chr15: 92,402,520-97,547,707 , GRCh37.p13 chr15: 92,945,750-98,090,937	, LOC105371004, 71 more genes
nsv5530569	copy number variation	1	nstd206	human		GRCh38 chr15: 96,785,839-96,789,808 , GRCh37.p13 chr15: 97,329,069-97,333,038	SPATA8
nsv5002607	copy number variation	1	nstd200	human		GRCh38 chr15: 96,782,598-96,783,226 , GRCh37.p13 chr15: 97,325,828-97,326,456	SPATA8, SPATA8-AS1
nsv4729092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189	CHD2, MIR11181, 272 more genes
nsv4675988	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 97,026,327-97,345,287 , GRCh38.p12 chr15: 96,483,097-96,802,057	LOC105371002, RN7SKP254, 4 more genes
nsv4675839	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 97,242,441-98,823,437 , GRCh38.p12 chr15: 96,699,211-98,280,208	SPATA8-AS1, LOC105371002, 19 more genes
nsv4675149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909	TTLL13, LINC00052, 264 more genes
nsv4578637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,878,099-102,397,836 , GRCh38.p12 chr15: 96,334,870-101,857,633	SYNM-AS1, LINC02253, 94 more genes
nsv4456430	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909	IQGAP1, LOC400464, 210 more genes
nsv4350607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,873,212-102,389,423 , GRCh38.p12 chr15: 96,329,983-101,849,220	LOC105371010, SELENOS, 95 more genes
nsv4251559	copy number variation	1	nstd166	human		GRCh37.p13 chr15: 97,296,409-97,336,929 , GRCh38.p12 chr15: 96,753,179-96,793,699	FAM149B1P1, SPATA8, 1 more genes
nsv4246966	copy number variation	1	nstd166	human		GRCh37.p13 chr15: 97,322,483-97,336,846 , GRCh38.p12 chr15: 96,779,253-96,793,616	SPATA8, SPATA8-AS1
nsv3924639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 94,576,237-102,383,473 , NCBI36 chr15: 92,377,241-100,200,996 , GRCh38 chr15: 94,033,008-101,843,270	RNU6-807P, LETR1, 119 more genes
nsv3923265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,567,356-102,461,201 , NCBI36 chr15: 94,368,360-100,278,724 , GRCh38 chr15: 96,024,127-101,920,998	LOC107987228, ARRDC4, 104 more genes
nsv3922914	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 92,814,458-100,338,915 , GRCh37.p13 chr15: 95,013,454-102,521,392 , GRCh38.p12 chr15: 94,470,225-101,981,189	OR4F14P, RNA5SP401, 124 more genes
nsv3922157	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189	GCHFR, SPPL2A, 1382 more genes
nsv3921313	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,313,856-102,351,195 , NCBI36 chr15: 94,114,860-100,168,718 , GRCh38 chr15: 95,770,627-101,810,992	SELENOS, SPATA8-AS1, 97 more genes
nsv3920352	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 83,711,377-101,843,270 , NCBI36 chr15: 82,171,133-100,200,996 , GRCh37 chr15: 84,380,129-102,383,473	LOC102724465, SNRPA1, 333 more genes
nsv3920248	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 87,618,716-100,262,146 , GRCh37.p13 chr15: 89,817,712-102,444,623 , GRCh38.p12 chr15: 89,274,481-101,904,420	FAM149B1P1, MIR9-3HG, 229 more genes

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Number of Variants: 20

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Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 137

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Number of Variants: 20

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