dbVar for Gene (Select 2302) - 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
nsv5328587	copy number variation	1	nstd204	human		GRCh38.p13 chr17: 76,133,059-76,134,651 , GRCh37.p13 chr17: 74,129,140-74,130,732	FOXJ1
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
nsv4680180	copy number variation	1	nstd189	human		GRCh37.p13 chr17: 74,053,616-74,648,486 , GRCh38.p12 chr17: 76,057,535-76,652,404	, AANAT, 30 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
nsv4632532	copy number variation	1	nstd183	human		GRCh37 chr17: 74,115,882-74,143,047 , GRCh38.p12 chr17: 76,119,801-76,146,966	RNF157, LOC101928447, 2 more genes
nsv4551528	insertion	1	nstd166	human		GRCh37.p13 chr17: 74,135,164-74,135,164 , GRCh38.p12 chr17: 76,139,083-76,139,083	FOXJ1, RNF157-AS1
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
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
nsv3958027	insertion	1	nstd168	human		GRCh38 chr17: 76,140,809-76,162,081 , GRCh37.p13 chr17: 74,136,890-74,158,162	FOXJ1, RNF157, 1 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
nsv3906075	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 67,002,415-81,041,938 , GRCh38.p12 chr17: 69,006,274-83,084,062	CEP131, RPTOR, 374 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	MIR3185, YWHAEP6, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	P4HB, LOC105371808, 2366 more genes

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Items: 1 to 20 of 131

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Number of Variants: 20

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