MS25589 AND nstd71 - dbVar - NCBI

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Items: 13

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Number of Variants: 13

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
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
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
nsv888231	copy number variation	61	nstd71	human		NCBI36 chr7: 62,366,659-62,440,767 , GRCh37.p13 chr7: 62,729,224-62,803,332 , GRCh38.p12 chr7: 63,268,846-63,342,954	ZNF733P, ARAFP3
nsv879318	copy number variation	371	nstd71	human		NCBI36 chr4: 69,085,989-69,179,871 , GRCh37.p13 chr4: 69,403,394-69,497,276 , GRCh38.p12 chr4: 68,537,676-68,631,558	LOC728807, UGT2B17, 2 more genes
nsv888239	copy number variation	20	nstd71	human		NCBI36 chr7: 62,499,511-62,572,772 , GRCh37.p13 chr7: 62,862,076-62,935,337 , GRCh38.p12 chr7: 63,401,698-63,474,959	VN1R33P, ARAFP2, 1 more genes
nsv883932	copy number variation	140	nstd71	human		NCBI36 chr6: 29,989,443-30,004,400 , GRCh37.p13 chr6: 29,881,464-29,896,421 , GRCh37.p13 chr6\|NT_167246.1: 1,175,640-1,190,626 , GRCh38.p12 chr6: 29,913,687-29,928,644 , GRCh38.p12 chr6\|NT_167246.2: 1,170,020-1,185,006	HLA-K, HCG4B, 1 more genes
nsv883580	copy number variation	22	nstd71	human		NCBI36 chr6: 29,957,666-29,988,619 , GRCh37.p13 chr6\|NT_167246.1: 1,157,859-1,174,816 , GRCh37.p13 chr6: 29,849,687-29,880,640 , GRCh38.p12 chr6: 29,881,910-29,912,863 , GRCh38.p12 chr6\|NT_167246.2: 1,152,239-1,169,196	HCG4P7, HLA-T, 5 more genes
nsv874634	copy number variation	114	nstd71	human		NCBI36 chr2: 89,721,421-89,911,010 , GRCh37.p13 chr2: 90,084,116-90,273,705 , GRCh38.p12 chr2: 90,045,284-90,234,838	IGKV3D-15, IGKV1D-16, 14 more genes
nsv905949	copy number variation	55	nstd71	human		NCBI36 chr16: 32,406,646-32,511,911 , GRCh37.p13 chr16: 32,499,145-32,604,410 , GRCh38.p12 chr16: 32,487,824-32,593,089	0
nsv885874	copy number variation	10	nstd71	human		NCBI36 chr6: 47,245,694-47,302,576 , GRCh37.p13 chr6: 47,137,735-47,194,617 , GRCh38.p12 chr6: 47,169,999-47,226,881	0
nsv878628	copy number variation	13	nstd71	human		NCBI36 chr4: 8,780,538-9,095,677 , GRCh37.p13 chr4: 8,729,638-9,486,579 , GRCh38.p12 chr4: 8,727,912-9,484,932	FAM86KP, DEFB108F, 42 more genes
nsv896324	copy number variation	16	nstd71	human		NCBI36 chr10: 135,075,656-135,252,190 , GRCh37.p13 chr10: 135,225,666-135,402,200 , GRCh38.p12 chr10: 133,412,162-133,588,696	SPRN, SPRNP1, 10 more genes

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