dbVar for Gene (Select 486) - 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
nsv7093918	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr11: 116,660,844-117,870,356 , GRCh38.p12 chr11: 116,790,128-117,999,641	PAFAH1B2, FXYD2, 26 more genes
nsv7093833	copy number variation	6	nstd102	human	Uncertain significance	GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563	RN7SL688P, MIR4492, 131 more genes
nsv7093753	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786	TMEM25, HYOU1, 93 more genes
nsv7062420	inversion	1	nstd229	human		GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444	RN7SL688P, MIR4492, 72 more genes
nsv6913051	copy number variation	1	nstd229	human		GRCh38 chr11: 117,816,019-117,818,525 , GRCh37.p13 chr11: 117,686,734-117,689,240	FXYD2, DSCAML1, 1 more genes
nsv6908595	copy number variation	1	nstd229	human		GRCh38 chr11: 117,823,347-117,826,291 , GRCh37.p13 chr11: 117,694,062-117,697,006	FXYD6-FXYD2, FXYD2
nsv6904371	copy number variation	1	nstd229	human		GRCh38 chr11: 117,798,101-117,821,832 , GRCh37.p13 chr11: 117,668,816-117,692,547	DSCAML1, FXYD6-FXYD2, 1 more genes
nsv6902051	copy number variation	1	nstd229	human		GRCh38 chr11: 117,622,062-117,860,669 , GRCh37.p13 chr11: 117,492,777-117,731,384	FXYD2, DSCAML1, 3 more genes
nsv6899779	copy number variation	1	nstd229	human		GRCh38 chr11: 117,824,625-117,854,524 , GRCh37.p13 chr11: 117,695,340-117,725,239	FXYD2, FXYD6, 1 more genes
nsv6455930	copy number variation	1	nstd223	human		GRCh38 chr11: 117,824,778-117,826,942 , GRCh37.p13 chr11: 117,695,493-117,697,657	FXYD2, FXYD6-FXYD2
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	PYGM, ATL3, 2125 more genes
nsv6308962	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563	LOC107984399, PCSK7, 132 more genes
nsv6291074	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847	ZW10, MPZL2, 378 more genes
nsv6290834	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956	CARD17P, RNA5SP350, 480 more genes
nsv6289927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522	IGSF9B, MIR10526, 592 more genes
nsv5505749	copy number variation	1	nstd206	human		GRCh38 chr11: 117,820,861-117,820,969 , GRCh37.p13 chr11: 117,691,576-117,691,684	FXYD6-FXYD2, FXYD2
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv4732750	copy number variation	1	nstd199	human		GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572	, LINC02702, 392 more genes
nsv4674572	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571	ACRV1, APLP2, 382 more genes
nsv4349506	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591	LOC107984407, DCPS, 394 more genes

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Items: 1 to 20 of 114

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Number of Variants: 20

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