SP52409 AND nstd71 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv898084	copy number variation	1	nstd71	human		NCBI36 chr11: 88,117,210-88,159,225 , GRCh37.p13 chr11: 88,477,562-88,519,577 , GRCh38.p12 chr11: 88,744,394-88,786,409	GRM5
nsv884852	copy number variation	234	nstd71	human		NCBI36 chr6: 32,561,832-32,593,470 , GRCh37.p13 chr6: 32,453,854-32,485,492 , GRCh38.p12 chr6: 32,486,077-32,517,715	HLA-DRB5
nsv899455	copy number variation	1	nstd71	human		NCBI36 chr12: 94,442,741-94,469,612 , GRCh37.p13 chr12: 95,918,610-95,945,481 , GRCh38.p12 chr12: 95,524,834-95,551,705	USP44
nsv897527	copy number variation	1	nstd71	human		NCBI36 chr11: 50,282,317-50,332,876 , GRCh37.p13 chr11: 50,325,741-50,376,300 , GRCh38.p12 chr11: 50,366,570-50,417,129	LOC646813
nsv887074	copy number variation	23	nstd71	human		NCBI36 chr7: 136,005-166,359 , GRCh37.p13 chr7: 40,922-71,276 , GRCh38.p12 chr7\|NT_187653.1: 36,223-63,597 , GRCh38.p12 chr7: 43,902-71,276 , GRCh38.p12 chr7\|NT_187558.1: 1-27,375	LOC105375113
nsv879345	copy number variation	351	nstd71	human		NCBI36 chr4: 69,117,497-69,179,871 , GRCh37.p13 chr4: 69,434,902-69,497,276 , GRCh38.p12 chr4: 68,569,184-68,631,558	UGT2B17, LOC100132651, 2 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
nsv870928	copy number variation	2	nstd71	human		NCBI36 chr1: 17,081,038-17,135,964 , GRCh37.p13 chr1: 17,208,451-17,263,377 , GRCh38.p12 chr1: 16,881,956-16,936,882	RNU1-2, LOC107985101, 3 more genes
nsv883820	copy number variation	14	nstd71	human		NCBI36 chr6: 29,978,470-30,001,440 , GRCh37.p13 chr6\|NT_167246.1: 1,164,662-1,187,711 , GRCh37.p13 chr6: 29,870,491-29,893,461 , GRCh38.p12 chr6\|NT_167246.2: 1,159,042-1,182,091 , GRCh38.p12 chr6: 29,902,714-29,925,684	HLA-K, HCG4B, 4 more genes
nsv903214	copy number variation	8	nstd71	human		NCBI36 chr15: 19,635,853-19,933,866 , GRCh37.p13 chr15: 21,371,194-22,432,502 , GRCh38.p12 chr15: 21,165,865-22,144,551	VN1R62P, MIR3118-3, 46 more genes
nsv890006	copy number variation	35	nstd71	human		NCBI36 chr8: 5,581,540-5,594,564 , GRCh37.p13 chr8: 5,594,132-5,607,156 , GRCh38.p12 chr8: 5,736,610-5,749,634	0
nsv884258	copy number variation	146	nstd71	human		NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,625,230	0
nsv875979	copy number variation	1	nstd71	human		NCBI36 chr2: 232,909,572-232,987,979 , GRCh37.p13 chr2: 233,201,328-233,279,735 , GRCh38.p12 chr2: 232,336,618-232,415,025	ECEL1P1, DIS3L2, 6 more genes
nsv901226	copy number variation	7	nstd71	human		NCBI36 chr14: 19,207,427-19,494,891 , GRCh37.p13 chr14: 20,137,587-20,425,051 , GRCh38.p12 chr14: 19,669,428-19,956,892	OR4M1, LOC100422528, 18 more genes
nsv890314	copy number variation	4	nstd71	human		NCBI36 chr8: 7,741,510-7,828,037 , GRCh37.p13 chr8: 7,704,100-7,790,627 , GRCh38.p12 chr8\|NW_018654717.1: 5,443,871-5,513,617 , GRCh38.p12 chr8: 7,846,578-7,933,105	DEFB4A, HSPD1P2, 7 more genes
nsv880984	copy number variation	2	nstd71	human		NCBI36 chr4: 179,636,517-179,657,951 , GRCh37.p13 chr4: 179,399,523-179,420,957 , GRCh38.p12 chr4: 178,478,369-178,499,803	0

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