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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5930898copy number variation1nstd209human GRCh38 chr19: 3,491,039-3,491,107 , GRCh37.p13 chr19: 3,491,037-3,491,105 LOC105372246, DOHH
    nsv5294162copy number variation1nstd204human GRCh38.p13 chr19: 3,332,801-3,820,800 , GRCh37.p13 chr19: 3,332,799-3,820,798 LOC105372245, LOC105372248, 19 more genes
    nsv5292408copy number variation1nstd204human GRCh38.p13 chr19: 2,552,101-4,875,100 , GRCh37.p13 chr19: 2,552,099-4,875,112 , S1PR4, 93 more genes
    nsv5290007copy number variation1nstd204human GRCh38.p13 chr19: 3,474,131-3,505,105 , GRCh37.p13 chr19: 3,474,129-3,505,103 LOC105372245, FZR1, 3 more genes
    nsv5288914copy number variation1nstd204human GRCh38.p13 chr19: 2,928,901-3,530,500 , GRCh37.p13 chr19: 2,928,899-3,530,498 LOC105372244, DOHH, 17 more genes
    nsv5163614mobile element insertion1nstd203human GRCh38 chr19: 3,489,855-3,489,868 , GRCh37.p13 chr19: 3,489,853-3,489,866 LOC105372246, DOHH
    nsv5019292copy number variation1nstd200human GRCh38 chr19: 3,494,032-3,495,265 , GRCh37.p13 chr19: 3,494,030-3,495,263 LOC105372245, DOHH
    nsv5019285copy number variation1nstd200human GRCh38 chr19: 3,412,536-3,513,755 , GRCh37.p13 chr19: 3,412,534-3,513,753 NFIC, FZR1, 4 more genes
    nsv5014346copy number variation1nstd200human GRCh38 chr19: 3,490,763-3,500,484 , GRCh37.p13 chr19: 3,490,761-3,500,482 LOC105372245, DOHH, 1 more genes
    nsv4852602copy number variation1nstd200human GRCh37 chr19: 3,488,775-3,489,217 , GRCh38.p12 chr19: 3,488,777-3,489,219 DOHH, LOC105372246
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4619086copy number variation1nstd183human GRCh37 chr19: 3,500,776-3,506,118 , GRCh38.p12 chr19: 3,500,778-3,506,120 DOHH, LOC105372245, 1 more genes
    nsv4457843copy number variation1nstd102humanUncertain significance GRCh37 chr19: 3,132,909-3,907,470 , GRCh38.p12 chr19: 3,132,911-3,907,472 LOC105372244, TEKTIP1, 27 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4457466copy number variation1nstd102humanUncertain significance GRCh37 chr19: 3,134,686-3,501,127 , GRCh38.p12 chr19: 3,134,688-3,501,129 NCLN, CELF5, 9 more genes
    nsv4452268copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,406,030-3,597,207 , GRCh38.p12 chr19: 1,406,031-3,597,209 C19orf25, MIR7108, 92 more genes
    nsv4436611copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,229,488-4,004,142 , GRCh38.p12 chr19: 2,229,489-4,004,144 LMNB2, SF3A2, 76 more genes
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