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Items: 1 to 20 of 448

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961293insertion1nstd209human GRCh38 chr6: 40,583,212-40,583,212 , GRCh37.p13 chr6: 40,550,951-40,550,951 LRFN2
    nsv5901808copy number variation1nstd209human GRCh38 chr6: 40,466,431-40,468,693 , GRCh37.p13 chr6: 40,434,170-40,436,432 LRFN2
    nsv5900795copy number variation1nstd209human GRCh38 chr6: 40,549,683-40,550,721 , GRCh37.p13 chr6: 40,517,422-40,518,460 LRFN2
    nsv5900569copy number variation1nstd209human GRCh38 chr6: 40,397,763-40,401,105 , GRCh37.p13 chr6: 40,365,502-40,368,844 LRFN2
    nsv5899127copy number variation1nstd209human GRCh38 chr6: 40,430,804-40,431,228 , GRCh37.p13 chr6: 40,398,543-40,398,967 LRFN2
    nsv5893536copy number variation1nstd209human GRCh38 chr6: 40,575,238-40,575,288 , GRCh37.p13 chr6: 40,542,977-40,543,027 LRFN2
    nsv5845603copy number variation1nstd209human GRCh38 chr6: 40,549,687-40,550,986 , GRCh37.p13 chr6: 40,517,426-40,518,725 LRFN2
    nsv5845602copy number variation1nstd209human GRCh38 chr6: 40,466,363-40,468,709 , GRCh37.p13 chr6: 40,434,102-40,436,448 LRFN2
    nsv5845503copy number variation1nstd209human GRCh38 chr6: 40,397,722-40,401,121 , GRCh37.p13 chr6: 40,365,461-40,368,860 LRFN2
    nsv5729621mobile element insertion2nstd211human GRCh38 chr6: 40,440,006-40,440,006 , GRCh37.p13 chr6: 40,407,745-40,407,745 LRFN2
    nsv5721434mobile element insertion2nstd211human GRCh38 chr6: 40,577,838-40,577,838 , GRCh37.p13 chr6: 40,545,577-40,545,577 LRFN2
    nsv5684519mobile element insertion1nstd211human GRCh38 chr6: 40,435,014-40,435,014 , GRCh37.p13 chr6: 40,402,753-40,402,753 LRFN2
    nsv5684209mobile element insertion1nstd211human GRCh38 chr6: 40,577,838-40,577,838 , GRCh37.p13 chr6: 40,545,577-40,545,577 LRFN2
    nsv5675833mobile element insertion1nstd211human GRCh38 chr6: 40,548,953-40,548,953 , GRCh37.p13 chr6: 40,516,692-40,516,692 LRFN2
    nsv5640368insertion1nstd207human GRCh38 chr6: 40,577,103-40,577,103 , GRCh37.p13 chr6: 40,544,842-40,544,842 LRFN2
    nsv5636661insertion1nstd207human GRCh38 chr6: 40,491,463-40,491,463 , GRCh37.p13 chr6: 40,459,202-40,459,202 LRFN2
    nsv5633493insertion1nstd207human GRCh38 chr6: 40,491,719-40,491,719 , GRCh37.p13 chr6: 40,459,458-40,459,458 LRFN2
    nsv5626583insertion1nstd207human GRCh38 chr6: 40,491,696-40,491,696 , GRCh37.p13 chr6: 40,459,435-40,459,435 LRFN2
    nsv5576482copy number variation1nstd207human GRCh38 chr6: 40,397,763-40,401,105 , GRCh37.p13 chr6: 40,365,502-40,368,844 LRFN2
    nsv5561846mobile element insertion1nstd206human GRCh38 chr6: 40,440,006-40,440,057 , GRCh37.p13 chr6: 40,407,745-40,407,796 LRFN2
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