SP50548 AND nstd71 - dbVar - NCBI

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Items: 9

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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
nsv886250	copy number variation	523	nstd71	human		NCBI36 chr6: 79,022,244-79,098,352 , GRCh37.p13 chr6: 78,965,525-79,041,633 , GRCh38.p12 chr6: 78,255,808-78,331,916	LOC105377865
nsv906988	copy number variation	1	nstd71	human		NCBI36 chr16: 77,557,145-77,573,909 , GRCh37.p13 chr16: 78,999,644-79,016,408 , GRCh38.p12 chr16: 78,965,747-78,982,511	WWOX
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
nsv900169	copy number variation	1	nstd71	human		NCBI36 chr13: 56,654,503-56,722,157 , GRCh37.p13 chr13: 57,756,502-57,824,156 , GRCh38.p12 chr13: 57,182,368-57,250,022	LOC105370216, MTCO2P3
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
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
nsv884814	copy number variation	27	nstd71	human		NCBI36 chr6: 32,560,168-32,576,147 , GRCh37.p13 chr6: 32,452,190-32,468,169 , GRCh38.p12 chr6: 32,484,413-32,500,392	0
nsv896361	copy number variation	17	nstd71	human		NCBI36 chr10: 135,106,317-135,235,772 , GRCh37.p13 chr10: 135,256,327-135,385,782 , GRCh38.p12 chr10: 133,442,823-133,572,278	CYP2E1, , 6 more genes

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