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Items: 1 to 20 of 288

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950739insertion1nstd209human GRCh38 chr4: 31,203,675-31,203,675 , GRCh37.p13 chr4: 31,205,297-31,205,297 LINC02497
    nsv5900162copy number variation1nstd209human GRCh38 chr4: 31,202,234-31,202,336 , GRCh37.p13 chr4: 31,203,856-31,203,958 LINC02497
    nsv5897491copy number variation1nstd209human GRCh38 chr4: 31,181,843-31,185,352 , GRCh37.p13 chr4: 31,183,465-31,186,974 LINC02497
    nsv5890827copy number variation1nstd209human GRCh38 chr4: 31,203,682-31,203,735 , GRCh37.p13 chr4: 31,205,304-31,205,357 LINC02497
    nsv5888824copy number variation1nstd209human GRCh38 chr4: 31,204,193-31,204,511 , GRCh37.p13 chr4: 31,205,815-31,206,133 LINC02497
    nsv5838982copy number variation1nstd209human GRCh38 chr4: 31,184,042-31,186,274 , GRCh37.p13 chr4: 31,185,664-31,187,896 LINC02497
    nsv5838933copy number variation1nstd209human GRCh38 chr4: 31,181,842-31,185,474 , GRCh37.p13 chr4: 31,183,464-31,187,096 LINC02497
    nsv5693961mobile element insertion1nstd211human GRCh38 chr4: 31,177,640-31,177,640 , GRCh37.p13 chr4: 31,179,262-31,179,262 LINC02497
    nsv5623456insertion1nstd207human GRCh38 chr4: 31,203,674-31,203,674 , GRCh37.p13 chr4: 31,205,296-31,205,296 LINC02497
    nsv5607665insertion1nstd207human GRCh38 chr4: 31,203,675-31,203,675 , GRCh37.p13 chr4: 31,205,297-31,205,297 LINC02497
    nsv5578124copy number variation1nstd207human GRCh38 chr4: 31,202,234-31,202,336 , GRCh37.p13 chr4: 31,203,856-31,203,958 LINC02497
    nsv5565493copy number variation1nstd207human GRCh38 chr4: 31,204,193-31,204,511 , GRCh37.p13 chr4: 31,205,815-31,206,133 LINC02497
    nsv5439408copy number variation1nstd206human GRCh38 chr4: 31,204,205-31,204,512 , GRCh37.p13 chr4: 31,205,827-31,206,134 LINC02497
    nsv5385369mobile element deletion2nstd186human GRCh37 chr4: 31,205,827-31,206,134 , GRCh38.p12 chr4: 31,204,205-31,204,512 LINC02497
    nsv5236029copy number variation1nstd204human GRCh38.p13 chr4: 31,204,201-31,204,500 , GRCh37.p13 chr4: 31,205,823-31,206,122 LINC02497
    nsv5210460mobile element deletion1nstd204human GRCh38.p13 chr4: 31,204,205-31,204,512 , GRCh37.p13 chr4: 31,205,827-31,206,134 LINC02497
    nsv5084421mobile element insertion1nstd203human GRCh38 chr4: 31,189,902-31,189,920 , GRCh37.p13 chr4: 31,191,524-31,191,542 LINC02497
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4889301mobile element deletion1nstd200human GRCh38 chr4: 31,204,205-31,204,512 , GRCh37.p13 chr4: 31,205,827-31,206,134 LINC02497
    nsv4778023mobile element deletion1nstd200human GRCh37 chr4: 31,205,827-31,206,134 , GRCh38.p12 chr4: 31,204,205-31,204,512 LINC02497
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