SP51290 AND nstd71 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv898220	copy number variation	20	nstd71	human		NCBI36 chr11: 97,321,440-97,396,117 , GRCh37.p13 chr11: 97,816,230-97,890,907 , GRCh38.p12 chr11: 97,945,230-98,020,179	LINC02713
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
nsv886922	copy number variation	6	nstd71	human		NCBI36 chr6: 165,037,385-165,128,459 , GRCh37.p13 chr6: 165,117,395-165,208,469 , GRCh38.p12 chr6: 164,696,362-164,794,980	MEAT6
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
nsv905993	copy number variation	10	nstd71	human		NCBI36 chr16: 32,410,369-32,579,320 , GRCh37.p13 chr16: 32,502,868-32,671,819 , GRCh38.p12 chr16: 32,491,547-32,660,498	LOC107984013, FAM153DP
nsv885398	copy number variation	7	nstd71	human		NCBI36 chr6: 32,638,176-32,664,508 , GRCh37.p13 chr6: 32,530,198-32,556,530 , GRCh38.p12 chr6: 32,562,421-32,588,753	HLA-DRB1, RNU1-152P
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 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
nsv876893	copy number variation	298	nstd71	human		NCBI36 chr3: 65,159,939-65,190,844 , GRCh37.p13 chr3: 65,184,899-65,215,804 , GRCh38.p12 chr3: 65,199,224-65,230,129	0
nsv901150	copy number variation	5	nstd71	human		NCBI36 chr14: 19,093,120-19,226,775 , GRCh37.p13 chr14: 20,023,120-20,156,935 , GRCh38.p12 chr14: 19,611,715-19,688,776	LOC100420171, USP10P1, 5 more genes
nsv901263	copy number variation	14	nstd71	human		NCBI36 chr14: 19,249,891-19,494,891 , GRCh37.p13 chr14: 20,180,051-20,425,051 , GRCh38.p12 chr14: 19,711,892-19,956,892	OR4K5, OR4K2, 13 more genes
nsv906993	copy number variation	1	nstd71	human		NCBI36 chr16: 78,441,351-78,480,811 , GRCh37.p13 chr16: 79,883,850-79,923,310 , GRCh38.p12 chr16: 79,849,953-79,889,413	0

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