dbVar for Gene (Select 283989) - 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
nsv5967778	inversion	1	nstd209	human		GRCh37.p13 chr17: 73,502,206-73,606,416 , GRCh38 chr17: 75,506,125-75,610,335	, LLGL2, 3 more genes
nsv5293343	copy number variation	1	nstd204	human		GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782	, RNU6-24P, 92 more genes
nsv4854394	copy number variation	1	nstd200	human		GRCh37 chr17: 73,511,580-73,714,116 , GRCh38.p12 chr17: 75,515,499-75,718,036	, CASKIN2, 8 more genes
nsv4676104	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963	LLGL2, TSEN54, 165 more genes
nsv4628995	copy number variation	1	nstd183	human		GRCh37 chr17: 73,217,773-73,774,243 , GRCh38.p12 chr17: 75,221,678-75,778,162	, LOC107985013, 23 more genes
nsv4623150	copy number variation	1	nstd183	human		GRCh37 chr17: 73,512,441-73,512,938 , GRCh38.p12 chr17: 75,516,360-75,516,857	TSEN54
nsv4457646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062	LOC107985089, ARSG, 448 more genes
nsv4457598	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 73,413,448-73,568,196 , GRCh38.p12 chr17: 75,417,367-75,572,115	MIR6785, LLGL2, 3 more genes
nsv4413616	copy number variation	1	nstd174	human		GRCh37 chr17: 73,513,262-73,542,824 , GRCh38.p12 chr17: 75,517,181-75,546,743	, LLGL2, 1 more genes
nsv4368627	copy number variation	2	nstd173	human		GRCh37 chr17: 73,514,076-73,713,995 , GRCh38.p12 chr17: 75,517,995-75,717,915	, MYO15B, 7 more genes
nsv4257584	copy number variation	1	nstd166	human		GRCh37.p13 chr17: 73,511,580-73,714,159 , GRCh38.p12 chr17: 75,515,499-75,718,079	, SMIM6, 8 more genes
nsv3972399	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942	AANAT, ACOX1, 243 more genes
nsv3919156	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717	CD300A, RNF213, 359 more genes
nsv3917654	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677	LOC101928447, GRB2, 368 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	LOC105371922, GJD3, 1855 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	PRPSAP1, CACNG1, 1350 more genes
nsv3909523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062	RPL38, RNF157-AS1, 428 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	FOXK2, SOCS3-DT, 958 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	SMURF2, LOC112268199, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	MIR21, LOC105371899, 2366 more genes

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Organism

Variant Type

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 198

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Number of Variants: 20

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