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Items: 1 to 20 of 471

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961574insertion1nstd209human GRCh38 chr2: 231,352,869-231,352,869 , GRCh37.p13 chr2: 232,217,581-232,217,581 ARMC9
    nsv5953101insertion1nstd209human GRCh38 chr2: 231,328,761-231,328,761 , GRCh37.p13 chr2: 232,193,473-232,193,473 ARMC9
    nsv5906396copy number variation1nstd209human GRCh38 chr2: 231,324,479-231,324,605 , GRCh37.p13 chr2: 232,189,191-232,189,317 ARMC9
    nsv5895438copy number variation1nstd209human GRCh38 chr2: 231,352,866-231,352,939 , GRCh37.p13 chr2: 232,217,578-232,217,651 ARMC9
    nsv5895167copy number variation1nstd209human GRCh38 chr2: 231,350,797-231,353,048 , GRCh37.p13 chr2: 232,215,509-232,217,760 ARMC9
    nsv5832782copy number variation2nstd209human GRCh38 chr2: 231,350,953-231,353,044 , GRCh37.p13 chr2: 232,215,665-232,217,756 ARMC9
    nsv5719551mobile element insertion1nstd211human GRCh38 chr2: 231,352,500-231,352,500 , GRCh37.p13 chr2: 232,217,212-232,217,212 ARMC9
    nsv5715234mobile element insertion2nstd211human GRCh38 chr2: 231,324,930-231,324,930 , GRCh37.p13 chr2: 232,189,642-232,189,642 ARMC9
    nsv5681956mobile element insertion1nstd211human GRCh38 chr2: 231,303,202-231,303,202 , GRCh37.p13 chr2: 232,167,915-232,167,915 ARMC9
    nsv5673613copy number variation1nstd102humanPathogenic GRCh37 chr2: 232,137,648-232,137,811 , GRCh38.p12 chr2: 231,272,935-231,273,098 ARMC9
    nsv5673535copy number variation1nstd102humanUncertain significance GRCh37 chr2: 232,220,490-232,225,614 , GRCh38.p12 chr2: 231,355,778-231,360,903 ARMC9, MIR4777
    nsv5621629insertion1nstd207human GRCh38 chr2: 231,353,566-231,353,566 , GRCh37.p13 chr2: 232,218,278-232,218,278 ARMC9
    nsv5582727copy number variation1nstd207human GRCh38 chr2: 231,249,801-231,249,948 , GRCh37.p13 chr2: 232,114,514-232,114,661 ARMC9
    nsv5579490copy number variation1nstd207human GRCh38 chr2: 231,381,185-231,381,268 , GRCh37.p13 chr2: 232,245,896-232,245,979 ARMC9
    nsv5568906copy number variation1nstd207human GRCh38 chr2: 231,381,437-231,381,503 , GRCh37.p13 chr2: 232,246,148-232,246,214 ARMC9
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5540948insertion1nstd206human GRCh38 chr2: 231,352,868-231,352,919 , GRCh37.p13 chr2: 232,217,580-232,217,631 ARMC9
    nsv5540572insertion1nstd206human GRCh38 chr2: 231,352,995-231,352,995 , GRCh37.p13 chr2: 232,217,707-232,217,707 ARMC9
    nsv5540476insertion1nstd206human GRCh38 chr2: 231,345,865-231,345,901 , GRCh37.p13 chr2: 232,210,577-232,210,613 ARMC9
    nsv5447380copy number variation1nstd206human GRCh38 chr2: 231,388,569-231,388,745 , GRCh37.p13 chr2: 232,253,280-232,253,456 ARMC9
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