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Items: 1 to 20 of 1448

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128983insertion1nstd186human GRCh37 chr4: 81,721,922-81,721,922 , GRCh38.p12 chr4: 80,800,768-80,800,768 CFAP299
    nsv5967615inversion1nstd209human GRCh38 chr4: 80,690,191-80,706,857 , GRCh37.p13 chr4: 81,611,345-81,628,011 CFAP299
    nsv5967091insertion1nstd209human GRCh38 chr4: 80,669,125-80,669,125 , GRCh37.p13 chr4: 81,590,279-81,590,279 CFAP299
    nsv5950479insertion1nstd209human GRCh38 chr4: 80,800,761-80,800,761 , GRCh37.p13 chr4: 81,721,915-81,721,915 CFAP299
    nsv5905456copy number variation1nstd209human GRCh38 chr4: 80,610,065-80,614,786 , GRCh37.p13 chr4: 81,531,219-81,535,940 CFAP299
    nsv5903401copy number variation1nstd209human GRCh38 chr4: 80,799,587-80,799,691 , GRCh37.p13 chr4: 81,720,741-81,720,845 CFAP299
    nsv5902742copy number variation1nstd209human GRCh38 chr4: 80,799,132-80,800,631 , GRCh37.p13 chr4: 81,720,286-81,721,785 CFAP299
    nsv5902167copy number variation1nstd209human GRCh38 chr4: 80,782,565-80,782,744 , GRCh37.p13 chr4: 81,703,719-81,703,898 CFAP299
    nsv5901967copy number variation1nstd209human GRCh38 chr4: 80,587,851-80,588,749 , GRCh37.p13 chr4: 81,509,005-81,509,903 CFAP299
    nsv5901432copy number variation1nstd209human GRCh38 chr4: 80,381,372-80,381,710 , GRCh37.p13 chr4: 81,302,526-81,302,864 CFAP299
    nsv5900918copy number variation1nstd209human GRCh38 chr4: 80,650,261-80,652,821 , GRCh37.p13 chr4: 81,571,415-81,573,975 CFAP299
    nsv5900723copy number variation1nstd209human GRCh38 chr4: 80,799,796-80,799,949 , GRCh37.p13 chr4: 81,720,950-81,721,103 CFAP299
    nsv5900243copy number variation1nstd209human GRCh38 chr4: 80,392,378-80,392,496 , GRCh37.p13 chr4: 81,313,532-81,313,650 CFAP299
    nsv5900097copy number variation1nstd209human GRCh38 chr4: 80,571,589-80,571,751 , GRCh37.p13 chr4: 81,492,743-81,492,905 CFAP299
    nsv5898497copy number variation1nstd209human GRCh38 chr4: 80,673,021-80,673,529 , GRCh37.p13 chr4: 81,594,175-81,594,683 CFAP299
    nsv5898424copy number variation1nstd209human GRCh38 chr4: 80,788,023-80,788,704 , GRCh37.p13 chr4: 81,709,177-81,709,858 CFAP299
    nsv5897068copy number variation1nstd209human GRCh38 chr4: 80,902,423-80,902,488 , GRCh37.p13 chr4: 81,823,577-81,823,642 CFAP299
    nsv5895044copy number variation1nstd209human GRCh38 chr4: 80,854,313-80,854,704 , GRCh37.p13 chr4: 81,775,467-81,775,858 CFAP299
    nsv5892026copy number variation1nstd209human GRCh38 chr4: 80,726,098-80,726,627 , GRCh37.p13 chr4: 81,647,252-81,647,781 CFAP299
    nsv5889703copy number variation1nstd209human GRCh38 chr4: 80,535,327-80,535,522 , GRCh37.p13 chr4: 81,456,481-81,456,676 CFAP299
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