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Items: 1 to 20 of 3753

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114528copy number variation1nstd186human GRCh37 chr15: 21,139,723-21,183,082 , GRCh38.p12 chr15: 20,934,394-20,977,753 OR11J2P, LINC01193, 3 more genes
    nsv5935377copy number variation1nstd209human GRCh38 chr15: 20,058,428-21,065,075 , GRCh37.p13 chr15: 20,263,681-21,270,404 , VN1R60P, 33 more genes
    nsv5380974copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,612,840-23,272,733 , GRCh38.p12 chr15: 20,407,587-22,308,242 OR11J2P, LOC105379205, 82 more genes
    nsv5279828copy number variation1nstd204human GRCh38.p13 chr15: 20,914,101-20,934,300 , GRCh37.p13 chr15: 21,119,430-21,139,629 NF1P1
    nsv5277643copy number variation1nstd204human GRCh38.p13 chr15: 20,928,101-20,929,300 , GRCh37.p13 chr15: 21,133,430-21,134,629 NF1P1
    nsv5277507copy number variation1nstd204human GRCh38.p13 chr15: 20,934,501-20,937,300 , GRCh37.p13 chr15: 21,139,830-21,142,629 NF1P1
    nsv5275337copy number variation1nstd204human GRCh38.p13 chr15: 20,935,401-20,939,100 , GRCh37.p13 chr15: 21,140,730-21,144,429 LINC01193, NF1P1, 1 more genes
    nsv5275330copy number variation1nstd204human GRCh38.p13 chr15: 20,929,801-20,932,200 , GRCh37.p13 chr15: 21,135,130-21,137,529 NF1P1
    nsv5273034copy number variation1nstd204human GRCh38.p13 chr15: 20,933,601-20,936,200 , GRCh37.p13 chr15: 21,138,930-21,141,529 NF1P1
    nsv5272680copy number variation1nstd204human GRCh38.p13 chr15: 20,914,101-20,928,200 , GRCh37.p13 chr15: 21,119,430-21,133,529 NF1P1
    nsv5271801copy number variation1nstd204human GRCh38.p13 chr15: 20,923,501-20,925,400 , GRCh37.p13 chr15: 21,128,830-21,130,729 NF1P1
    nsv5270527copy number variation1nstd204human GRCh38.p13 chr15: 20,924,801-20,925,400 , GRCh37.p13 chr15: 21,130,130-21,130,729 NF1P1
    nsv5270295copy number variation1nstd204human GRCh38.p13 chr15: 20,915,101-20,915,500 , GRCh37.p13 chr15: 21,120,430-21,120,829 NF1P1
    nsv5270222copy number variation1nstd204human GRCh38.p13 chr15: 20,926,101-20,931,500 , GRCh37.p13 chr15: 21,131,430-21,136,829 NF1P1
    nsv5268326copy number variation1nstd204human GRCh37.p13 chr15: 21,026,530-21,139,929 , GRCh38.p13 chr15: 20,821,201-20,934,600 POTEB2, ZNF519P2, 5 more genes
    nsv5268212copy number variation1nstd204human GRCh38.p13 chr15: 20,933,001-20,934,200 , GRCh37.p13 chr15: 21,138,330-21,139,529 NF1P1
    nsv5266466copy number variation1nstd204human GRCh38.p13 chr15: 20,893,701-20,926,900 , GRCh37.p13 chr15: 21,099,030-21,132,229 NF1P1, VN1R61P, 1 more genes
    nsv5266243copy number variation1nstd204human GRCh38.p13 chr15: 20,916,001-20,916,700 , GRCh37.p13 chr15: 21,121,330-21,122,029 NF1P1
    nsv5264755copy number variation1nstd204human GRCh38.p13 chr15: 20,929,801-20,934,300 , GRCh37.p13 chr15: 21,135,130-21,139,629 NF1P1
    nsv5262306copy number variation1nstd204human GRCh38.p13 chr15: 20,931,101-20,932,200 , GRCh37.p13 chr15: 21,136,430-21,137,529 NF1P1
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