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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123775copy number variation1nstd186human GRCh37 chr19: 49,958,329-49,958,719 , GRCh38.p12 chr19: 49,455,072-49,455,462 ALDH16A1
    nsv5940492copy number variation1nstd209human GRCh38 chr19: 49,455,020-49,455,317 , GRCh37.p13 chr19: 49,958,277-49,958,574 ALDH16A1
    nsv5936794copy number variation1nstd209human GRCh38 chr19: 49,456,918-49,458,023 , GRCh37.p13 chr19: 49,960,175-49,961,280 ALDH16A1
    nsv5929683copy number variation1nstd209human GRCh38 chr19: 49,465,497-49,465,596 , GRCh37.p13 chr19: 49,968,754-49,968,853 ALDH16A1
    nsv5884354copy number variation1nstd209human GRCh38 chr19: 49,456,876-49,458,001 , GRCh37.p13 chr19: 49,960,133-49,961,258 ALDH16A1
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5660146insertion1nstd207human GRCh38 chr19: 49,461,541-49,461,541 , GRCh37.p13 chr19: 49,964,798-49,964,798 ALDH16A1
    nsv5655938insertion1nstd207human GRCh38 chr19: 49,455,070-49,455,070 , GRCh37.p13 chr19: 49,958,327-49,958,327 ALDH16A1
    nsv5654353insertion2nstd207human GRCh38 chr19: 49,461,540-49,461,540 , GRCh37.p13 chr19: 49,964,797-49,964,797 ALDH16A1
    nsv5652954insertion1nstd207human GRCh38 chr19: 49,461,298-49,461,298 , GRCh37.p13 chr19: 49,964,555-49,964,555 ALDH16A1
    nsv5594506copy number variation1nstd207human GRCh38 chr19: 49,463,208-49,463,425 , GRCh37.p13 chr19: 49,966,465-49,966,682 ALDH16A1
    nsv5590078copy number variation1nstd207human GRCh38 chr19: 49,463,462-49,463,679 , GRCh37.p13 chr19: 49,966,719-49,966,936 ALDH16A1
    nsv5523155copy number variation1nstd206human GRCh38 chr19: 49,455,072-49,455,462 , GRCh37.p13 chr19: 49,958,329-49,958,719 ALDH16A1
    nsv5389568copy number variation1nstd186human GRCh37 chr19: 49,964,324-49,964,852 , GRCh38.p12 chr19: 49,461,067-49,461,595 ALDH16A1
    nsv5166787mobile element insertion1nstd203human GRCh38 chr19: 49,462,233-49,462,244 , GRCh37.p13 chr19: 49,965,490-49,965,501 ALDH16A1
    nsv4865259copy number variation1nstd200human GRCh37 chr19: 49,964,317-49,964,946 , GRCh38.p12 chr19: 49,461,060-49,461,689 ALDH16A1
    nsv4731479copy number variation1nstd199human GRCh37 chr19: 49,966,115-49,966,690 , GRCh38.p12 chr19: 49,462,858-49,463,433 ALDH16A1
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4726124insertion1nstd186human GRCh37 chr19: 49,958,305-49,958,305 , GRCh38.p12 chr19: 49,455,048-49,455,048 ALDH16A1
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
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