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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979328inversion1nstd209human GRCh38 chr19: 32,019,307-33,218,671 , GRCh37.p13 chr19: 32,510,213-33,709,577 , LRP3, 28 more genes
    nsv5944157copy number variation1nstd209human GRCh38 chr19: 32,858,843-32,859,153 , GRCh37.p13 chr19: 33,349,749-33,350,059 SLC7A9
    nsv5939271copy number variation1nstd209human GRCh38 chr19: 32,847,982-32,848,098 , GRCh37.p13 chr19: 33,338,888-33,339,004 SLC7A9
    nsv5532723copy number variation1nstd206human GRCh38 chr19: 32,847,982-32,848,116 , GRCh37.p13 chr19: 33,338,888-33,339,022 SLC7A9
    nsv5527279copy number variation1nstd206human GRCh38 chr19: 32,839,314-32,841,454 , GRCh37.p13 chr19: 33,330,220-33,332,360 SLC7A9
    nsv5525920copy number variation1nstd206human GRCh38 chr19: 32,855,677-32,857,174 , GRCh37.p13 chr19: 33,346,583-33,348,080 SLC7A9
    nsv5518016copy number variation1nstd206human GRCh38 chr19: 32,854,815-32,856,502 , GRCh37.p13 chr19: 33,345,721-33,347,408 SLC7A9
    nsv5514931copy number variation1nstd206human GRCh38 chr19: 32,831,914-32,832,036 , GRCh37.p13 chr19: 33,322,820-33,322,942 SLC7A9
    nsv5325065copy number variation1nstd204human GRCh38.p13 chr19: 32,853,757-32,855,525 , GRCh37.p13 chr19: 33,344,663-33,346,431 SLC7A9
    nsv5287271copy number variation1nstd204human GRCh38.p13 chr19: 32,853,928-32,855,427 , GRCh37.p13 chr19: 33,344,834-33,346,333 SLC7A9
    nsv5020348copy number variation1nstd200human GRCh38 chr19: 32,854,698-32,855,692 , GRCh37.p13 chr19: 33,345,604-33,346,598 SLC7A9
    nsv5020347copy number variation1nstd200human GRCh38 chr19: 32,839,314-32,841,454 , GRCh37.p13 chr19: 33,330,220-33,332,360 SLC7A9
    nsv5020346copy number variation1nstd200human GRCh38 chr19: 32,833,165-32,838,067 , GRCh37.p13 chr19: 33,324,071-33,328,973 SLC7A9
    nsv4861254copy number variation1nstd200human GRCh37 chr19: 33,346,598-33,347,996 , GRCh38.p12 chr19: 32,855,692-32,857,090 SLC7A9
    nsv4861253copy number variation1nstd200human GRCh37 chr19: 33,344,672-33,346,423 , GRCh38.p12 chr19: 32,853,766-32,855,517 SLC7A9
    nsv4861252copy number variation1nstd200human GRCh37 chr19: 33,330,220-33,332,360 , GRCh38.p12 chr19: 32,839,314-32,841,454 SLC7A9
    nsv4861251copy number variation1nstd200human GRCh37 chr19: 33,324,071-33,328,973 , GRCh38.p12 chr19: 32,833,165-32,838,067 SLC7A9
    nsv4681430copy number variation1nstd102humanPathogenic GRCh37 chr19: 33,324,035-33,324,249 , GRCh38.p12 chr19: 32,833,129-32,833,343 SLC7A9
    nsv4679951copy number variation1nstd189human GRCh37.p13 chr19: 33,011,549-33,386,125 , GRCh38.p12 chr19: 32,520,643-32,895,219 , PDCD5, 11 more genes
    nsv4630664copy number variation1nstd183human GRCh37 chr19: 33,345,838-33,491,120 , GRCh38.p12 chr19: 32,854,932-33,000,214 SLC7A9, CEP89, 4 more genes
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