dbVar for Gene (Select 100533181) - 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
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
nsv5500379	copy number variation	1	nstd206	human		GRCh38 chr11: 117,867,187-117,872,813 , GRCh37.p13 chr11: 117,737,902-117,743,528	FXYD6-FXYD2, FXYD6
nsv5495719	copy number variation	1	nstd206	human		GRCh38 chr11: 117,857,859-117,857,925 , GRCh37.p13 chr11: 117,728,574-117,728,640	FXYD6, FXYD6-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
nsv4989346	copy number variation	1	nstd200	human		GRCh38 chr11: 117,857,085-117,947,830 , GRCh37.p13 chr11: 117,727,800-117,818,545	FXYD6, FXYD6-FXYD2, 1 more genes
nsv4989345	copy number variation	1	nstd200	human		GRCh38 chr11: 117,843,046-117,920,750 , GRCh37.p13 chr11: 117,713,761-117,791,465	FXYD6-FXYD2, TMPRSS13, 1 more genes
nsv4847673	copy number variation	1	nstd200	human		GRCh37 chr11: 117,713,761-117,791,465 , GRCh38.p12 chr11: 117,843,046-117,920,750	FXYD6, TMPRSS13, 1 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
nsv4349045	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169	MPZL3, ADAMTS8, 393 more genes
nsv4211035	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 117,729,470-117,729,524 , GRCh38.p12 chr11: 117,858,755-117,858,809	FXYD6-FXYD2, FXYD6
nsv4209248	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 117,686,656-117,689,243 , GRCh38.p12 chr11: 117,815,941-117,818,528	FXYD6-FXYD2, FXYD2, 1 more genes
nsv4209165	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 117,713,666-117,714,030 , GRCh38.p12 chr11: 117,842,951-117,843,315	FXYD6-FXYD2, FXYD6
nsv3962404	copy number variation	1	nstd168	human		GRCh38 chr11: 117,772,582-117,818,891 , GRCh37.p13 chr11: 117,643,297-117,689,606	, FXYD2, 2 more genes
nsv3960881	copy number variation	1	nstd168	human		GRCh38 chr11: 117,867,827-117,903,272 , GRCh37.p13 chr11: 117,738,542-117,773,987	FXYD6-FXYD2, TMPRSS13, 1 more genes
nsv3923375	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,722,088-134,868,420 , NCBI36 chr11: 116,227,298-134,373,630 , GRCh38 chr11: 116,851,372-134,998,526	VPS26B, LOC105369531, 390 more genes
nsv3922253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246	RPS27P19, UBASH3B, 655 more genes
nsv3916857	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr11: 116,227,321-134,373,617 , GRCh37 chr11: 116,722,111-134,868,407 , GRCh38 chr11: 116,851,395-134,998,513	RPUSD4, ELOCP22, 390 more genes
nsv3914316	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 115,812,352-117,422,156 , GRCh38 chr11: 116,436,425-118,046,231 , GRCh37 chr11: 116,307,142-117,916,946	LOC653303, BUD13, 31 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 180

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Number of Variants: 20

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