SP55302 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
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
nsv893272	copy number variation	8	nstd71	human		NCBI36 chr9: 43,614,077-43,730,292 , GRCh37.p13 chr9: 43,674,081-43,790,296 , GRCh38.p12 chr9: 42,024,093-42,140,308	CNTNAP3B, LOC100420440
nsv897049	copy number variation	2	nstd71	human		NCBI36 chr11: 21,848,419-22,250,522 , GRCh37.p13 chr11: 21,891,843-22,293,946 , GRCh38.p12 chr11: 21,870,297-22,272,400	ANO5, LOC105376587, 1 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
nsv907907	copy number variation	2	nstd71	human		NCBI36 chr17: 21,319,218-21,480,206 , GRCh37.p13 chr17\|NW_003315950.2: 127,678-288,723 , GRCh37.p13 chr17: 21,381,527-21,529,632 , GRCh38.p12 chr17: 21,475,313-21,636,358	LOC105371589, LOC100533653, 3 more genes
nsv882131	copy number variation	3	nstd71	human		NCBI36 chr5: 70,311,476-70,443,650 , GRCh37.p13 chr5: 70,275,720-70,407,894 , GRCh38.p12 chr5: 70,979,893-71,112,067	NAIPP4, OCLNP1, 4 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
nsv906475	copy number variation	8	nstd71	human		NCBI36 chr16: 32,475,644-32,511,911 , GRCh37.p13 chr16: 32,568,143-32,604,410 , GRCh38.p12 chr16: 32,556,822-32,593,089	0

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