dbVar for Gene (Select 55334) - 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
nsv5980451	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321	ACTN1, ACYP1, 400 more genes
nsv5939901	copy number variation	1	nstd209	human		GRCh38 chr14: 69,413,167-69,423,709 , GRCh37.p13 chr14: 69,879,884-69,890,426	SLC39A9
nsv5852198	copy number variation	1	nstd209	human		GRCh38 chr14: 69,413,055-69,423,652 , GRCh37.p13 chr14: 69,879,772-69,890,369	SLC39A9
nsv5537136	insertion	1	nstd206	human		GRCh38 chr14: 69,411,792-69,411,792 , GRCh37.p13 chr14: 69,878,509-69,878,509	SLC39A9
nsv5494815	copy number variation	1	nstd206	human		GRCh38 chr14: 69,388,434-69,422,608 , GRCh37.p13 chr14: 69,855,151-69,889,325	SLC39A9, ERH
nsv5357366	translocation	1	nstd200	human		GRCh38 chr14: 69,433,778-69,433,778 , GRCh38 chr14: 69,433,861-69,433,861 , GRCh37.p13 chr14: 69,900,495-69,900,495 , GRCh37.p13 chr14: 69,900,578-69,900,578	SLC39A9
nsv5032025	inversion	1	nstd200	human		GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221	, IFT43, 578 more genes
nsv5004739	copy number variation	1	nstd200	human		GRCh38 chr14: 69,455,117-69,512,736 , GRCh37.p13 chr14: 69,921,834-69,979,453	SLC39A9, PLEKHD1
nsv4999875	copy number variation	1	nstd200	human		GRCh38 chr14: 69,460,876-69,470,111 , GRCh37.p13 chr14: 69,927,593-69,936,828	SLC39A9, PLEKHD1
nsv4999874	copy number variation	1	nstd200	human		GRCh38 chr14: 69,431,155-69,434,200 , GRCh37.p13 chr14: 69,897,872-69,900,917	SLC39A9
nsv4625461	copy number variation	1	nstd183	human		GRCh37 chr14: 69,918,377-69,976,706 , GRCh38.p12 chr14: 69,451,660-69,509,989	PLEKHD1, SLC39A9
nsv4503595	mobile element insertion	1	nstd166	human		GRCh37.p13 chr14: 69,900,016-69,900,016 , GRCh38.p12 chr14: 69,433,299-69,433,299	SLC39A9
nsv4499189	mobile element insertion	1	nstd166	human		GRCh37.p13 chr14: 69,881,793-69,881,793 , GRCh38.p12 chr14: 69,415,076-69,415,076	SLC39A9
nsv4456840	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr14: 69,921,280-69,976,359 , GRCh38.p12 chr14: 69,454,563-69,509,642	SLC39A9, PLEKHD1
nsv4378057	copy number variation	1	nstd173	human		GRCh37 chr14: 69,922,860-69,976,328 , GRCh38.p12 chr14: 69,456,143-69,509,611	SLC39A9, PLEKHD1
nsv4323072	inversion	1	nstd166	human		GRCh37.p13 chr14: 66,260,597-70,789,330 , GRCh38.p12 chr14: 65,793,879-70,322,613	, ACTN1, 81 more genes
nsv4219730	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 69,873,736-69,875,982 , GRCh38.p12 chr14: 69,407,019-69,409,265	SLC39A9
nsv4213811	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 69,870,738-69,879,061 , GRCh38.p12 chr14: 69,404,021-69,412,344	SLC39A9
nsv4213404	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 69,921,874-69,979,482 , GRCh38.p12 chr14: 69,455,157-69,512,765	SLC39A9, PLEKHD1
nsv3969921	copy number variation	1	nstd168	human		GRCh38 chr14: 69,391,231-69,420,484 , GRCh37.p13 chr14: 69,857,948-69,887,201	ERH, SLC39A9

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Number of Variants: 20

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Items: 1 to 20 of 184

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Number of Variants: 20

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