MS21477 AND nstd71 - dbVar - NCBI

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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
nsv872108	copy number variation	59	nstd71	human		NCBI36 chr1: 105,833,927-106,065,063 , GRCh37.p13 chr1: 106,032,404-106,263,540 , GRCh38.p12 chr1: 105,489,782-105,720,918	LOC105378881, SEPTIN2P1, 2 more genes
nsv876413	copy number variation	4	nstd71	human		NCBI36 chr3: 3,878,887-4,076,356 , GRCh37.p13 chr3: 3,903,887-4,101,356 , GRCh38.p12 chr3: 3,862,203-4,059,672	PNPT1P1, SUMF1, 2 more genes
nsv893207	copy number variation	32	nstd71	human		NCBI36 chr9: 43,532,092-43,730,292 , GRCh37.p13 chr9: 43,592,096-43,790,296 , GRCh38.p12 chr9: 42,024,093-42,222,293	PTS-P1, CNTNAP3B, 3 more genes
nsv889165	copy number variation	13	nstd71	human		NCBI36 chr7: 125,395,114-125,579,136 , GRCh37.p13 chr7: 125,607,878-125,791,900 , GRCh38.p12 chr7: 125,967,824-126,151,846	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
nsv873943	copy number variation	269	nstd71	human		NCBI36 chr2: 41,083,802-41,109,046 , GRCh37.p13 chr2: 41,230,298-41,255,542 , GRCh38.p12 chr2: 41,003,158-41,028,402	0
nsv904280	copy number variation	1	nstd71	human		NCBI36 chr15: 57,830,014-58,311,317 , GRCh37.p13 chr15: 60,042,722-60,524,025 , GRCh38.p12 chr15: 59,750,523-60,231,826	LOC105370838, , 7 more genes
nsv904254	copy number variation	1	nstd71	human		NCBI36 chr15: 55,490,245-57,808,929 , GRCh37.p13 chr15: 57,702,953-60,021,637 , GRCh38.p12 chr15: 57,410,755-59,729,438	ALDH1A2, RNU4-80P, 46 more genes

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