SP57037 AND nstd71 - dbVar - NCBI

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Number of Variants: 8

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
nsv908425	copy number variation	235	nstd71	human		NCBI36 chr17: 41,785,962-41,922,658 , GRCh37.p13 chr17: 44,430,206-44,566,775 , GRCh38.p12 chr17: 46,352,840-46,489,976	NSFP1, ARL17B
nsv906279	copy number variation	1	nstd71	human		NCBI36 chr16: 32,445,732-32,579,320 , GRCh37.p13 chr16: 32,538,231-32,671,819 , GRCh38.p12 chr16: 32,526,910-32,660,498	FAM153DP, LOC107984013
nsv908541	copy number variation	15	nstd71	human		NCBI36 chr17: 41,990,116-42,143,493 , GRCh37.p13 chr17: 44,634,800-44,788,310 , GRCh38.p12 chr17: 46,557,434-46,710,944	NSF, LRRC37A2, 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
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
nsv893230	copy number variation	100	nstd71	human		NCBI36 chr9: 43,570,503-44,683,090 , GRCh37.p13 chr9: 43,630,507-44,743,094 , GRCh38.p12 chr9: 41,912,139-42,974,549	CYP4F60P, RBPJP6, 30 more genes
nsv897299	copy number variation	1	nstd71	human		NCBI36 chr11: 42,400,487-42,479,942 , GRCh37.p13 chr11: 42,443,911-42,523,366 , GRCh38.p12 chr11: 42,422,361-42,501,816	0

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