IS33651 AND nstd71 - dbVar - NCBI

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Items: 10

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv886250	copy number variation	523	nstd71	human		NCBI36 chr6: 79,022,244-79,098,352 , GRCh37.p13 chr6: 78,965,525-79,041,633 , GRCh38.p12 chr6: 78,255,808-78,331,916	LOC105377865
nsv890751	copy number variation	169	nstd71	human		NCBI36 chr8: 39,350,791-39,497,557 , GRCh37.p13 chr8: 39,231,634-39,378,400 , GRCh38.p12 chr8: 39,374,115-39,520,881	ADAM5, ADAM3A
nsv881673	copy number variation	95	nstd71	human		NCBI36 chr5: 9,953,083-9,981,862 , GRCh37.p13 chr5: 9,900,083-9,928,862 , GRCh38.p12 chr5: 9,899,971-9,928,750	LOC107986405, LINC02112
nsv899837	copy number variation	61	nstd71	human		NCBI36 chr13: 18,427,644-18,524,818 , GRCh37.p13 chr13: 19,529,644-19,626,818 , GRCh38.p12 chr13: 18,955,504-19,052,678	USP24P1, PHF2P2, 3 more genes
nsv890340	copy number variation	6	nstd71	human		NCBI36 chr8: 9,066,823-9,158,808 , GRCh37.p13 chr8: 9,029,413-9,121,398 , GRCh38.p12 chr8: 9,171,903-9,263,888 , GRCh38.p12 chr8\|NW_018654717.1: 4,087,774-4,179,678	LOC101929128, LOC112268404, 1 more genes
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv884251	copy number variation	5	nstd71	human		NCBI36 chr6: 31,388,175-31,396,472 , GRCh37.p13 chr6: 31,280,196-31,288,493 , GRCh37.p13 chr6\|NT_167249.1: 2,613,906-2,622,207 , GRCh37.p13 chr6\|NT_167246.1: 2,627,015-2,631,393 , GRCh38.p12 chr6\|NT_167249.2: 2,614,608-2,622,909 , GRCh38.p12 chr6\|NT_167246.2: 2,621,395-2,625,775 , GRCh38.p12 chr6: 31,312,419-31,320,716	0
nsv871388	copy number variation	3	nstd71	human		NCBI36 chr1: 103,911,245-104,070,228 , GRCh37.p13 chr1: 104,109,722-104,268,705 , GRCh38.p12 chr1: 103,567,100-103,726,083	AMY1B, AMY2B, 5 more genes
nsv910218	copy number variation	2	nstd71	human		NCBI36 chr19: 539,860-612,080 , GRCh37.p13 chr19: 588,860-661,080 , GRCh38.p12 chr19: 588,860-661,080	HCN2, POLRMT, 5 more genes
nsv901292	copy number variation	51	nstd71	human		NCBI36 chr14: 19,261,709-19,486,339 , GRCh37.p13 chr14: 20,191,869-20,416,499 , GRCh38.p12 chr14: 19,723,710-19,948,340	OR4N2, OR4Q3, 11 more genes

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