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Items: 1 to 20 of 1530

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978424inversion1nstd209human GRCh38 chr2: 143,416,508-143,417,040 , GRCh37.p13 chr2: 144,174,077-144,174,609 ARHGAP15
    nsv5968086inversion1nstd209human GRCh38 chr2: 143,315,905-143,317,048 , GRCh37.p13 chr2: 144,073,474-144,074,617 ARHGAP15
    nsv5968034inversion1nstd209human GRCh38 chr2: 143,314,127-143,314,256 , GRCh37.p13 chr2: 144,071,696-144,071,825 ARHGAP15
    nsv5963955insertion1nstd209human GRCh38 chr2: 143,673,747-143,673,747 , GRCh37.p13 chr2: 144,431,316-144,431,316 ARHGAP15, ARHGAP15-AS1
    nsv5957204insertion1nstd209human GRCh38 chr2: 143,253,209-143,253,209 , GRCh37.p13 chr2: 144,010,778-144,010,778 ARHGAP15
    nsv5906725copy number variation1nstd209human GRCh38 chr2: 143,210,262-143,210,961 , GRCh37.p13 chr2: 143,967,831-143,968,530 ARHGAP15
    nsv5902749copy number variation1nstd209human GRCh38 chr2: 143,102,884-143,103,146 , GRCh37.p13 chr2: 143,860,453-143,860,715 ARHGAP15
    nsv5902380copy number variation1nstd209human GRCh38 chr2: 143,320,866-143,321,128 , GRCh37.p13 chr2: 144,078,435-144,078,697 ARHGAP15
    nsv5900608copy number variation1nstd209human GRCh38 chr2: 143,087,121-143,087,202 , GRCh37.p13 chr2: 143,844,690-143,844,771 ARHGAP15
    nsv5900576copy number variation1nstd209human GRCh38 chr2: 143,654,247-143,658,268 , GRCh37.p13 chr2: 144,411,816-144,415,837 ARHGAP15, ARHGAP15-AS1
    nsv5899939copy number variation1nstd209human GRCh38 chr2: 143,194,861-143,194,923 , GRCh37.p13 chr2: 143,952,430-143,952,492 ARHGAP15
    nsv5898949copy number variation1nstd209human GRCh38 chr2: 143,555,860-143,555,909 , GRCh37.p13 chr2: 144,313,429-144,313,478 ARHGAP15
    nsv5896011copy number variation1nstd209human GRCh38 chr2: 143,264,439-143,264,498 , GRCh37.p13 chr2: 144,022,008-144,022,067 ARHGAP15
    nsv5895444copy number variation1nstd209human GRCh38 chr2: 143,123,054-143,129,105 , GRCh37.p13 chr2: 143,880,623-143,886,674 ARHGAP15
    nsv5895146copy number variation1nstd209human GRCh38 chr2: 143,756,885-143,759,858 , GRCh37.p13 chr2: 144,514,454-144,517,427 ARHGAP15
    nsv5893234copy number variation1nstd209human GRCh38 chr2: 143,526,104-143,526,425 , GRCh37.p13 chr2: 144,283,673-144,283,994 ARHGAP15
    nsv5893025copy number variation1nstd209human GRCh38 chr2: 143,168,570-143,170,144 , GRCh37.p13 chr2: 143,926,139-143,927,713 ARHGAP15, LOC107985949
    nsv5891397copy number variation1nstd209human GRCh38 chr2: 143,165,990-143,166,040 , GRCh37.p13 chr2: 143,923,559-143,923,609 ARHGAP15
    nsv5891110copy number variation1nstd209human GRCh38 chr2: 143,169,703-143,169,762 , GRCh37.p13 chr2: 143,927,272-143,927,331 ARHGAP15, LOC107985949
    nsv5890852copy number variation1nstd209human GRCh38 chr2: 143,471,180-143,471,229 , GRCh37.p13 chr2: 144,228,749-144,228,798 ARHGAP15
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