dbVar for Gene (Select 257364) - 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
nsv5933606	copy number variation	1	nstd209	human		GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573	, STRA6, 229 more genes
nsv5928357	copy number variation	1	nstd209	human		GRCh38 chr15: 75,270,339-75,786,969 , GRCh37.p13 chr15: 75,562,680-76,079,310	LOC101929408, RN7SL319P, 23 more genes
nsv5380975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 75,596,353-76,103,430 , GRCh38.p12 chr15: 75,304,012-75,811,089	RPL13P4, PTPN9, 20 more genes
nsv5380758	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289	LOC105370794, HNRNPA1P45, 1173 more genes
nsv4992298	copy number variation	1	nstd200	human		GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519	, SNUPN, 215 more genes
nsv4729733	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 75,920,400-76,632,051 , GRCh38.p12 chr15: 75,628,059-76,339,710	ISL2, TYRO3P, 18 more genes
nsv4729106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753	FAM219B, MIR4513, 62 more genes
nsv4728988	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 75,440,382-76,133,553 , GRCh38.p12 chr15: 75,148,041-75,841,212	RPL13P4, PTPN9, 30 more genes
nsv4456751	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 75,508,057-76,128,091 , GRCh38.p12 chr15: 75,215,716-75,835,750	GOLGA6C, COMMD4, 27 more genes
nsv4455912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,963,271-76,064,900 , GRCh38.p12 chr15: 72,670,930-75,772,559	MIR6881, ARID3B, 94 more genes
nsv4382078	copy number variation	1	nstd173	human		GRCh37 chr15: 75,877,215-75,991,451 , GRCh38.p12 chr15: 75,584,874-75,699,110	SNUPN, CSPG4, 2 more genes
nsv4370284	copy number variation	2	nstd173	human		GRCh37 chr15: 75,877,357-75,974,622 , GRCh38.p12 chr15: 75,585,016-75,682,281	SNUPN, CSPG4, 2 more genes
nsv4349273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 75,648,132-76,102,251 , GRCh38.p12 chr15: 75,355,791-75,809,910	SNUPN, GOLGA6EP, 17 more genes
nsv4247829	copy number variation	1	nstd166	human		GRCh37.p13 chr15: 75,831,948-75,952,401 , GRCh38.p12 chr15: 75,539,607-75,660,060	SNUPN, SNX33, 2 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
nsv3920020	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 72,685,231-75,727,625 , NCBI36 chr15: 70,764,625-73,807,021 , GRCh37 chr15: 72,977,572-76,019,966	STRA6, LOC105370891, 91 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	RNU6-18P, GOLGA8K, 1442 more genes
nsv3918770	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	SNRPCP18, SNORD116-30, 1622 more genes
nsv3918644	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	SNORD116-23, UBE2Q2P6, 1622 more genes
nsv3917589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724	GAPDHP61, SNORD18B, 840 more genes

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Number of Variants: 20

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dbVar

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

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Items: 1 to 20 of 149

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Number of Variants: 20

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