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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
    nsv5906978copy number variation1nstd209human GRCh38 chr2: 160,194,288-160,194,933 , GRCh37.p13 chr2: 161,050,799-161,051,444 ITGB6
    nsv5831900copy number variation1nstd209human GRCh38 chr2: 160,194,264-160,195,263 , GRCh37.p13 chr2: 161,050,775-161,051,774 ITGB6
    nsv5831702copy number variation1nstd209human GRCh38 chr2: 160,146,042-160,147,463 , GRCh37.p13 chr2: 161,002,553-161,003,974 ITGB6
    nsv5690819mobile element insertion1nstd211human GRCh38 chr2: 160,174,783-160,174,783 , GRCh37.p13 chr2: 161,031,294-161,031,294 ITGB6
    nsv5685851mobile element insertion1nstd211human GRCh38 chr2: 160,191,210-160,191,210 , GRCh37.p13 chr2: 161,047,721-161,047,721 ITGB6
    nsv5568627copy number variation1nstd207human GRCh38 chr2: 160,120,294-160,120,687 , GRCh37.p13 chr2: 160,976,805-160,977,198 ITGB6
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5451576copy number variation1nstd206human GRCh38 chr2: 160,134,907-160,152,532 , GRCh37.p13 chr2: 160,991,418-161,009,043 ITGB6
    nsv5449594copy number variation1nstd206human GRCh38 chr2: 160,192,360-160,194,791 , GRCh37.p13 chr2: 161,048,871-161,051,302 ITGB6
    nsv5442612copy number variation1nstd206human GRCh38 chr2: 160,119,000-160,135,618 , GRCh37.p13 chr2: 160,975,511-160,992,129 ITGB6
    nsv5441006copy number variation1nstd206human GRCh38 chr2: 160,120,274-160,120,777 , GRCh37.p13 chr2: 160,976,785-160,977,288 ITGB6
    nsv5439256copy number variation1nstd206human GRCh38 chr2: 160,165,919-160,165,977 , GRCh37.p13 chr2: 161,022,430-161,022,488 ITGB6
    nsv5439152copy number variation1nstd206human GRCh38 chr2: 160,194,295-160,194,934 , GRCh37.p13 chr2: 161,050,806-161,051,445 ITGB6
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5396461mobile element insertion1nstd206human GRCh38 chr2: 160,174,783-160,174,834 , GRCh37.p13 chr2: 161,031,294-161,031,345 ITGB6
    nsv5393981mobile element insertion1nstd206human GRCh38 chr2: 160,191,210-160,191,261 , GRCh37.p13 chr2: 161,047,721-161,047,772 ITGB6
    nsv5382445copy number variation1nstd186human GRCh37 chr2: 160,976,845-160,977,241 , GRCh38.p12 chr2: 160,120,334-160,120,730 ITGB6
    nsv5350913translocation1nstd200human GRCh38 chr2: 160,194,295-160,194,295 , GRCh38 chr2: 160,194,934-160,194,934 , GRCh37.p13 chr2: 161,050,806-161,050,806 , GRCh37.p13 chr2: 161,051,445-161,051,445 ITGB6
    nsv5343326translocation1nstd200human GRCh37 chr2: 161,050,806-161,050,806 , GRCh37 chr2: 161,051,445-161,051,445 , GRCh38.p12 chr2: 160,194,934-160,194,934 , GRCh38.p12 chr2: 160,194,295-160,194,295 ITGB6
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