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Items: 1 to 20 of 683

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921323copy number variation1nstd209human GRCh38 chr9: 130,876,782-130,877,851 , GRCh37.p13 chr9: 133,752,169-133,753,238 ABL1
    nsv5916037copy number variation1nstd209human GRCh38 chr9: 130,876,717-130,877,896 , GRCh37.p13 chr9: 133,752,104-133,753,283 ABL1
    nsv5913226copy number variation1nstd209human GRCh38 chr9: 130,813,098-130,813,443 , GRCh37.p13 chr9: 133,688,485-133,688,830 ABL1
    nsv5911826copy number variation1nstd209human GRCh38 chr9: 130,731,173-130,735,195 , GRCh37.p13 chr9: 133,606,560-133,610,582 ABL1
    nsv5911134copy number variation1nstd209human GRCh38 chr9: 130,717,763-130,718,066 , GRCh37.p13 chr9: 133,593,150-133,593,453 ABL1
    nsv5865376copy number variation1nstd209human GRCh38 chr9: 130,731,788-130,733,887 , GRCh37.p13 chr9: 133,607,175-133,609,274 ABL1
    nsv5857677copy number variation1nstd209human GRCh38 chr9: 130,813,990-130,816,589 , GRCh37.p13 chr9: 133,689,377-133,691,976 ABL1
    nsv5857600copy number variation1nstd209human GRCh38 chr9: 130,730,588-130,732,487 , GRCh37.p13 chr9: 133,605,975-133,607,874 ABL1
    nsv5849082copy number variation1nstd209human GRCh38 chr9: 130,876,726-130,877,825 , GRCh37.p13 chr9: 133,752,113-133,753,212 ABL1
    nsv5704717mobile element insertion1nstd211human GRCh38 chr9: 130,834,123-130,834,123 , GRCh37.p13 chr9: 133,709,510-133,709,510 ABL1
    nsv5634895insertion1nstd207human GRCh38 chr9: 130,777,807-130,777,807 , GRCh37.p13 chr9: 133,653,194-133,653,194 ABL1
    nsv5629426insertion1nstd207human GRCh38 chr9: 130,778,048-130,778,048 , GRCh37.p13 chr9: 133,653,435-133,653,435 ABL1
    nsv5603407copy number variation1nstd207human GRCh38 chr9: 130,777,774-130,777,849 , GRCh37.p13 chr9: 133,653,161-133,653,236 ABL1
    nsv5601336copy number variation1nstd207human GRCh38 chr9: 130,777,546-130,777,849 , GRCh37.p13 chr9: 133,652,933-133,653,236 ABL1
    nsv5587830copy number variation1nstd207human GRCh38 chr9: 130,876,745-130,877,807 , GRCh37.p13 chr9: 133,752,132-133,753,194 ABL1
    nsv5493580copy number variation1nstd206human GRCh38 chr9: 130,811,891-130,813,221 , GRCh37.p13 chr9: 133,687,278-133,688,608 ABL1
    nsv5491103copy number variation1nstd206human GRCh38 chr9: 130,777,444-130,778,334 , GRCh37.p13 chr9: 133,652,831-133,653,721 ABL1
    nsv5490451copy number variation1nstd206human GRCh38 chr9: 130,749,728-130,750,266 , GRCh37.p13 chr9: 133,625,115-133,625,653 ABL1
    nsv5488612copy number variation1nstd206human GRCh38 chr9: 130,744,177-130,745,096 , GRCh37.p13 chr9: 133,619,564-133,620,483 ABL1
    nsv5487695copy number variation1nstd206human GRCh38 chr9: 130,819,438-130,819,522 , GRCh37.p13 chr9: 133,694,825-133,694,909 ABL1
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