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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067785inversion1nstd229human GRCh38 chr15: 48,330,359-48,330,445 , GRCh37.p13 chr15: 48,622,556-48,622,642 DUT
    nsv6972444copy number variation1nstd229human GRCh38 chr15: 48,310,948-48,333,561 , GRCh37.p13 chr15: 48,603,145-48,625,758 , DUT, 1 more genes
    nsv6970682copy number variation1nstd229human GRCh38 chr15: 48,308,949-48,436,880 , GRCh37.p13 chr15: 48,601,146-48,729,077 , DUT, 2 more genes
    nsv6970623copy number variation1nstd229human GRCh38 chr15: 48,343,805-48,347,589 , GRCh37.p13 chr15: 48,636,002-48,639,786 DUT
    nsv6969399copy number variation1nstd229human GRCh38 chr15: 48,334,055-48,335,636 , GRCh37.p13 chr15: 48,626,252-48,627,833 DUT
    nsv6969277copy number variation1nstd229human GRCh38 chr15: 48,292,501-48,333,000 , GRCh37.p13 chr15: 48,584,698-48,625,197 , DUT-AS1, 2 more genes
    nsv6959771copy number variation1nstd229human GRCh38 chr15: 48,330,411-48,330,457 , GRCh37.p13 chr15: 48,622,608-48,622,654 DUT
    nsv6959571copy number variation1nstd229human GRCh38 chr15: 48,338,114-48,341,416 , GRCh37.p13 chr15: 48,630,311-48,633,613 DUT
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6586820inversion1nstd223human GRCh38 chr15: 48,329,363-48,329,512 , GRCh37.p13 chr15: 48,621,560-48,621,709 DUT
    nsv6502580copy number variation1nstd223human GRCh38 chr15: 48,321,974-48,347,244 , GRCh37.p13 chr15: 48,614,171-48,639,441 DUT-AS1, DUT
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 PYGO1, RNU6-449P, 125 more genes
    nsv6309791copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,426,485-48,730,124 , GRCh38.p12 chr15: 48,134,288-48,437,927 DUT, FBN1, 6 more genes
    nsv6291615copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,179,968-48,727,846 , GRCh38.p12 chr15: 47,887,771-48,435,649 LOC102724553, CTXN2-AS1, 9 more genes
    nsv6132954copy number variation1nstd213human GRCh37 chr15: 48,580,000-48,770,001 , GRCh38.p12 chr15: 48,287,803-48,477,804 , DUT, 3 more genes
    nsv6039306copy number variation1nstd212human GRCh38 chr15: 48,329,010-48,329,314 , GRCh37.p13 chr15: 48,621,207-48,621,511 DUT
    nsv5694516mobile element insertion2nstd211human GRCh38 chr15: 48,340,637-48,340,637 , GRCh37.p13 chr15: 48,632,834-48,632,834 DUT
    nsv5529901copy number variation1nstd206human GRCh38 chr15: 48,321,985-48,347,244 , GRCh37.p13 chr15: 48,614,182-48,639,441 DUT, DUT-AS1
    nsv5523913copy number variation1nstd206human GRCh38 chr15: 48,343,252-48,344,599 , GRCh37.p13 chr15: 48,635,449-48,636,796 DUT
    nsv5432069mobile element insertion1nstd206human GRCh38 chr15: 48,340,637-48,340,688 , GRCh37.p13 chr15: 48,632,834-48,632,885 DUT
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