dbVar for Gene (Select 9899) - 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
nsv7148092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689	RPL9P8, COMMD4P1, 547 more genes
nsv7137910	insertion	1	nstd232	human		GRCh37.p13 chr15: 91,814,321-91,814,321 , GRCh38.p12 chr15: 91,271,091-91,271,091	SV2B
nsv7098897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098	LINC00933, DNM1P9, 540 more genes
nsv7098892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387	CIB1, RPS12P26, 326 more genes
nsv7069101	inversion	1	nstd229	human		GRCh38 chr15: 91,190,330-91,200,946 , GRCh37.p13 chr15: 91,733,560-91,744,176	SV2B
nsv7067417	inversion	1	nstd229	human		GRCh38 chr15: 91,190,560-91,194,972 , GRCh37.p13 chr15: 91,733,790-91,738,202	SV2B
nsv7065612	inversion	1	nstd229	human		GRCh38 chr15: 89,041,442-91,616,740 , GRCh37.p13 chr15: 89,584,673-92,159,970	ZNF774, CRAT37, 77 more genes
nsv6977143	copy number variation	1	nstd229	human		GRCh38 chr15: 91,270,801-91,280,200 , GRCh37.p13 chr15: 91,814,031-91,823,430	SV2B
nsv6976510	copy number variation	1	nstd229	human		GRCh38 chr15: 86,730,503-91,149,191 , GRCh37.p13 chr15: 87,273,734-91,692,421	, IQGAP1, 105 more genes
nsv6975364	copy number variation	1	nstd229	human		GRCh38 chr15: 91,232,318-91,865,076 , GRCh37.p13 chr15: 91,775,548-92,408,306	LOC105370972, THRAP3P2, 7 more genes
nsv6973886	copy number variation	1	nstd229	human		GRCh38 chr15: 91,278,375-91,282,096 , GRCh37.p13 chr15: 91,821,605-91,825,326	SV2B
nsv6972359	copy number variation	1	nstd229	human		GRCh38 chr15: 91,238,985-91,239,010 , GRCh37.p13 chr15: 91,782,215-91,782,240	SV2B, LOC105370972
nsv6972048	copy number variation	1	nstd229	human		GRCh38 chr15: 91,291,805-91,291,946 , GRCh37.p13 chr15: 91,835,035-91,835,176	SV2B
nsv6970149	copy number variation	1	nstd229	human		GRCh38 chr15: 91,212,245-91,212,846 , GRCh37.p13 chr15: 91,755,475-91,756,076	SV2B
nsv6969217	copy number variation	1	nstd229	human		GRCh38 chr15: 91,254,350-91,254,485 , GRCh37.p13 chr15: 91,797,580-91,797,715	LOC105370972, SV2B
nsv6968634	copy number variation	1	nstd229	human		GRCh38 chr15: 91,148,582-91,151,889 , GRCh37.p13 chr15: 91,691,812-91,695,119	SV2B
nsv6967444	copy number variation	1	nstd229	human		GRCh38 chr15: 91,259,832-91,267,233 , GRCh37.p13 chr15: 91,803,062-91,810,463	SV2B
nsv6967171	copy number variation	1	nstd229	human		GRCh38 chr15: 91,228,174-91,234,577 , GRCh37.p13 chr15: 91,771,404-91,777,807	SV2B, LOC105370972
nsv6965317	copy number variation	1	nstd229	human		GRCh38 chr15: 91,216,295-91,223,348 , GRCh37.p13 chr15: 91,759,525-91,766,578	SV2B
nsv6961826	copy number variation	1	nstd229	human		GRCh38 chr15: 91,234,501-91,252,200 , GRCh37.p13 chr15: 91,777,731-91,795,430	LOC105370972, SV2B

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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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Subject Phenotype Status

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Items: 1 to 20 of 507

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Number of Variants: 20

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