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Items: 1 to 20 of 946

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146469copy number variation1nstd232human GRCh37.p13 chr12: 40,864,969-40,865,090 , GRCh38.p12 chr12: 40,471,167-40,471,288 MUC19
    nsv7142702insertion1nstd232human GRCh37.p13 chr12: 40,884,241-40,884,241 , GRCh38.p12 chr12: 40,490,439-40,490,439 MUC19
    nsv7074054inversion1nstd229human GRCh38 chr12: 40,495,674-40,515,098 , GRCh37.p13 chr12: 40,889,476-40,908,900 MUC19
    nsv7073961inversion1nstd229human GRCh38 chr12: 40,392,805-40,398,943 , GRCh37.p13 chr12: 40,786,607-40,792,745 LOC105369736, MUC19
    nsv7073411inversion1nstd229human GRCh38 chr12: 40,483,174-40,483,280 , GRCh37.p13 chr12: 40,876,976-40,877,082 MUC19
    nsv7073204inversion1nstd229human GRCh38 chr12: 40,450,746-40,450,778 , GRCh37.p13 chr12: 40,844,548-40,844,580 MUC19
    nsv7072509inversion1nstd229human GRCh38 chr12: 40,398,793-40,407,353 , GRCh37.p13 chr12: 40,792,595-40,801,155 MUC19, LOC105369736
    nsv7070811inversion1nstd229human GRCh38 chr12: 40,417,296-40,417,342 , GRCh37.p13 chr12: 40,811,098-40,811,144 LOC105369736, MUC19
    nsv7069491inversion1nstd229human GRCh38 chr12: 38,629,739-41,866,812 , GRCh37.p13 chr12: 39,023,541-42,260,614 CPNE8, LOC100421126, 29 more genes
    nsv7068539inversion1nstd229human GRCh38 chr12: 40,446,833-40,480,883 , GRCh37.p13 chr12: 40,840,635-40,874,685 MUC19, LOC100420584
    nsv7068088inversion1nstd229human GRCh38 chr12: 40,410,173-40,410,199 , GRCh37.p13 chr12: 40,803,975-40,804,001 LOC105369736, MUC19
    nsv7064484inversion1nstd229human GRCh38 chr12: 40,417,269-40,498,006 , GRCh37.p13 chr12: 40,811,071-40,891,808 MUC19, LOC105369736, 1 more genes
    nsv7060676inversion1nstd229human GRCh38 chr12: 40,476,719-40,476,766 , GRCh37.p13 chr12: 40,870,521-40,870,568 MUC19
    nsv6934896copy number variation1nstd229human GRCh38 chr12: 40,471,001-40,489,800 , GRCh37.p13 chr12: 40,864,803-40,883,602 LOC100420584, MUC19
    nsv6934775copy number variation1nstd229human GRCh38 chr12: 40,418,039-40,420,692 , GRCh37.p13 chr12: 40,811,841-40,814,494 LOC105369736, MUC19
    nsv6934722copy number variation1nstd229human GRCh38 chr12: 40,393,601-40,398,100 , GRCh37.p13 chr12: 40,787,403-40,791,902 MUC19, LOC105369736
    nsv6934101copy number variation1nstd229human GRCh38 chr12: 39,893,726-40,431,148 , GRCh37.p13 chr12: 40,287,528-40,824,950 LINC02555, LOC105369735, 9 more genes
    nsv6933875copy number variation1nstd229human GRCh38 chr12: 40,422,601-40,427,800 , GRCh37.p13 chr12: 40,816,403-40,821,602 LOC105369736, MUC19
    nsv6933313copy number variation1nstd229human GRCh38 chr12: 40,418,986-40,438,615 , GRCh37.p13 chr12: 40,812,788-40,832,417 LOC105369736, MUC19
    nsv6933132copy number variation1nstd229human GRCh38 chr12: 40,471,201-40,560,400 , GRCh37.p13 chr12: 40,865,003-40,954,202 LOC100420584, MUC19, 1 more genes
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