MS21465 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
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
nsv882827	copy number variation	1	nstd71	human		NCBI36 chr5: 124,895,722-124,971,800 , GRCh37.p13 chr5: 124,867,823-124,943,901 , GRCh38.p12 chr5: 125,532,130-125,608,208	LINC02240
nsv898426	copy number variation	1	nstd71	human		NCBI36 chr11: 120,641,814-120,711,564 , GRCh37.p13 chr11: 121,136,604-121,206,354 , GRCh38.p12 chr11: 121,265,895-121,335,645	SC5D
nsv881588	copy number variation	3	nstd71	human		NCBI36 chr4: 162,058,162-162,102,577 , GRCh37.p13 chr4: 161,838,712-161,883,127 , GRCh38.p12 chr4: 160,917,560-160,961,975	LOC105377513
nsv898791	copy number variation	12	nstd71	human		NCBI36 chr12: 11,367,992-11,457,533 , GRCh37.p13 chr12: 11,476,725-11,566,266 , GRCh38.p12 chr12: 11,323,791-11,413,332 , GRCh38.p12 chr12\|NT_187658.1: 518,754-572,349	PRB2, PRB1
nsv905278	copy number variation	1	nstd71	human		NCBI36 chr16: 6,778,399-7,038,654 , GRCh37.p13 chr16: 6,838,398-7,098,653 , GRCh38.p12 chr16: 6,788,397-7,048,652	LOC105371068, RNU6-328P, 2 more genes
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
nsv885536	copy number variation	17	nstd71	human		NCBI36 chr6: 32,708,781-32,732,638 , GRCh37.p13 chr6\|NT_167249.1: 4,034,248-4,046,862 , GRCh37.p13 chr6\|NT_167246.1: 4,056,958-4,069,536 , GRCh37.p13 chr6: 32,600,803-32,624,660 , GRCh37.p13 chr6\|NT_167247.1: 3,939,666-3,952,277 , GRCh37.p13 chr6\|NT_167245.1: 3,882,525-3,895,103 , GRCh38.p12 chr6\|NT_167247.2: 3,934,081-3,946,695 , GRCh38.p12 chr6\|NT_167245.2: 3,876,940-3,889,518 , GRCh38.p12 chr6: 32,633,026-32,656,883 , GRCh38.p12 chr6\|NT_167249.2: 4,034,950-4,047,564 , GRCh38.p12 chr6\|NT_167246.2: 4,051,338-4,063,916	, , 2 more genes
nsv871302	copy number variation	40	nstd71	human		NCBI36 chr1: 12,771,679-12,810,136 , GRCh37.p13 chr1: 12,849,092-12,887,549 , GRCh38.p12 chr1: 12,788,951-12,827,690	LINC01784, PRAMEF11, 1 more genes
nsv886057	copy number variation	200	nstd71	human		NCBI36 chr6: 67,065,007-67,111,682 , GRCh37.p13 chr6: 67,008,286-67,054,961 , GRCh38.p12 chr6: 66,298,393-66,345,068	0
nsv895538	copy number variation	101	nstd71	human		NCBI36 chr10: 58,562,281-58,608,558 , GRCh37.p13 chr10: 58,892,275-58,938,552 , GRCh38.p12 chr10: 57,132,515-57,178,792	0
nsv901386	copy number variation	15	nstd71	human		NCBI36 chr14: 19,317,620-19,486,339 , GRCh37.p13 chr14: 20,247,780-20,416,499 , GRCh38.p12 chr14: 19,779,621-19,948,340	LOC100421751, OR4N1P, 8 more genes
nsv905911	copy number variation	5	nstd71	human		NCBI36 chr16: 32,405,464-32,511,911 , GRCh37.p13 chr16: 32,497,963-32,604,410 , GRCh38.p12 chr16: 32,486,642-32,593,089	0

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