MS19466 AND nstd71 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv905671	copy number variation	20	nstd71	human		NCBI36 chr16: 22,635,346-22,696,351 , GRCh37.p13 chr16: 22,727,845-22,788,850 , GRCh38.p12 chr16\|NW_017852933.1: 1,882,665-1,927,115 , GRCh38.p12 chr16: 22,716,524-22,777,529	LOC112268374
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv895761	copy number variation	319	nstd71	human		NCBI36 chr10: 81,462,715-81,497,813 , GRCh37.p13 chr10: 81,472,521-81,507,631 , GRCh38.p12 chr10: 79,712,765-79,747,875	NUTM2B, NUTM2B-AS1
nsv878549	copy number variation	2	nstd71	human		NCBI36 chr4: 7,346,055-7,427,595 , GRCh37.p13 chr4: 7,295,154-7,376,694 , GRCh38.p12 chr4: 7,293,427-7,374,967	SORCS2, MIR4798, 1 more genes
nsv915403	copy number variation	1	nstd71	human		NCBI36 chr22: 46,637,346-46,721,405 , GRCh37.p13 chr22: 48,258,682-48,342,741 , GRCh38.p12 chr22: 47,862,933-47,946,992	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
nsv872320	copy number variation	3	nstd71	human		NCBI36 chr1: 147,292,384-147,655,013 , GRCh37.p13 chr1: 149,025,760-149,388,389 , GRCh38.p12 chr1: 143,531,138-143,893,810	TRN-GTT12-1, PDE4DIPP3, 23 more genes
nsv901296	copy number variation	150	nstd71	human		NCBI36 chr14: 19,261,709-19,494,891 , GRCh37.p13 chr14: 20,191,869-20,425,051 , GRCh38.p12 chr14: 19,723,710-19,956,892	OR4K16P, OR4K2, 12 more genes

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