gosr1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3919950	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 24,298,969-27,841,151 , GRCh37 chr17: 27,274,843-30,817,038 , GRCh38 chr17: 28,947,825-32,490,020	GOSR1, MIR365B, 105 more genes
nsv7095086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139	GOSR1, LOC107984990, 59 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	GOSR1, MIR3185, 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	GOSR1, P4HB, 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	GOSR1, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	GOSR1, SMURF2, 2366 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	GOSR1, LOC105371922, 1855 more genes
nsv4457831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395	GOSR1, LOC105371753, 474 more genes
nsv3972367	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 25,403,446-31,685,464 , GRCh38.p12 chr17: 27,076,420-33,358,446	GOSR1, ASIC2, 190 more genes
nsv3903658	copy number variation	1	nstd102	human	drug response	GRCh37 chr17: 25,248,166-30,645,676 , GRCh38.p12 chr17: 26,935,981-32,318,657	GOSR1, KRT18P55, 179 more genes
nsv7095084	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155	GOSR1, RNU6-1267P, 114 more genes
nsv3912501	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 25,695,019-25,965,168 , GRCh37.p13 chr17: 28,670,893-28,941,042 , GRCh38.p12 chr17: 30,343,875-30,614,024	GOSR1, KRT17P3, 8 more genes

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