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Items: 1 to 20 of 317

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975397insertion1nstd209human GRCh38 chr16: 80,971,505-80,971,505 , GRCh37.p13 chr16: 81,005,402-81,005,402 CMC2
    nsv5968371insertion1nstd209human GRCh38 chr16: 80,990,172-80,990,172 , GRCh37.p13 chr16: 81,023,777-81,023,777 CMC2
    nsv5938793copy number variation1nstd209human GRCh38 chr16: 80,920,239-80,965,653 , GRCh37.p13 chr16: 80,954,136-80,999,550 CMC2
    nsv5927981copy number variation1nstd209human GRCh38 chr16: 81,001,903-81,003,042 , GRCh37.p13 chr16: 81,035,508-81,036,647 CMC2
    nsv5877101copy number variation1nstd209human GRCh38 chr16: 80,948,864-80,965,682 , GRCh37.p13 chr16: 80,982,761-80,999,579 CMC2
    nsv5730085mobile element insertion1nstd211human GRCh38 chr16: 80,993,717-80,993,717 , GRCh37.p13 chr16: 81,027,322-81,027,322 CMC2
    nsv5722616mobile element insertion1nstd211human GRCh38 chr16: 80,996,352-80,996,352 , GRCh37.p13 chr16: 81,029,957-81,029,957 CMC2
    nsv5591903copy number variation1nstd207human GRCh38 chr16: 80,980,230-80,980,521 , GRCh37.p13 chr16: 81,014,127-81,014,273 CMC2
    nsv5558109mobile element insertion1nstd206human GRCh38 chr16: 80,993,717-80,993,768 , GRCh37.p13 chr16: 81,027,322-81,027,373 CMC2
    nsv5548748insertion1nstd206human GRCh38 chr16: 80,990,188-80,990,215 , GRCh37.p13 chr16: 81,023,793-81,023,820 CMC2
    nsv5526349copy number variation1nstd206human GRCh38 chr16: 80,994,508-80,994,573 , GRCh37.p13 chr16: 81,028,113-81,028,178 CMC2
    nsv5525910copy number variation1nstd206human GRCh38 chr16: 80,981,252-80,981,340 , GRCh37.p13 chr16: 81,014,857-81,014,945 CMC2
    nsv5519936copy number variation1nstd206human GRCh38 chr16: 80,963,584-80,995,518 , GRCh37.p13 chr16: 80,997,481-81,029,123 CMC2
    nsv5518867copy number variation1nstd206human GRCh38 chr16: 80,287,955-81,045,090 , GRCh37.p13 chr16: 80,321,852-81,078,695 , DYNLRB2-AS1, 8 more genes
    nsv5518431copy number variation1nstd206human GRCh38 chr16: 80,920,262-80,965,654 , GRCh37.p13 chr16: 80,954,159-80,999,551 CMC2
    nsv5374726translocation1nstd200human GRCh38 chr16: 80,920,325-80,920,325 , GRCh38 chr16: 80,965,629-80,965,629 , GRCh37.p13 chr16: 80,954,222-80,954,222 , GRCh37.p13 chr16: 80,999,526-80,999,526 CMC2
    nsv5358422translocation1nstd200human GRCh38 chr16: 80,982,854-80,982,854 , GRCh38 chr16: 80,982,959-80,982,959 , GRCh37.p13 chr16: 81,016,564-81,016,564 , GRCh37.p13 chr16: 81,016,459-81,016,459 CMC2
    nsv5354199translocation1nstd200human GRCh38 chr10: 12,737,230-12,737,230 , GRCh38 chr16: 80,965,139-80,965,139 , GRCh37.p13 chr16: 80,999,036-80,999,036 , GRCh37.p13 chr10: 12,779,229-12,779,229 CMC2, CAMK1D
    nsv5336081translocation1nstd200human GRCh37 chr16: 81,016,564-81,016,564 , GRCh37 chr16: 81,016,459-81,016,459 , GRCh38.p12 chr16: 80,982,854-80,982,854 , GRCh38.p12 chr16: 80,982,959-80,982,959 CMC2
    nsv5297335copy number variation1nstd204human GRCh38.p13 chr16: 80,980,301-80,980,600 , GRCh37.p13 chr: NaN-NaN CMC2
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