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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148191copy number variation1nstd102humanUncertain significance GRCh38 chr13: 25,567,155-25,574,530 , GRCh37.p13 chr13: 26,141,293-26,148,668 ATP8A2
    nsv7143548copy number variation1nstd232human GRCh37.p13 chr13: 26,087,091-26,087,139 , GRCh38.p12 chr13: 25,512,953-25,513,001 ATP8A2
    nsv7142186insertion1nstd232human GRCh37.p13 chr13: 26,183,703-26,183,703 , GRCh38.p12 chr13: 25,609,565-25,609,565 ATP8A2
    nsv7141937insertion1nstd232human GRCh37.p13 chr13: 25,991,623-25,991,623 , GRCh38.p12 chr13: 25,417,485-25,417,485 ATP8A2
    nsv7140311insertion1nstd232human GRCh37.p13 chr13: 26,183,672-26,183,672 , GRCh38.p12 chr13: 25,609,534-25,609,534 ATP8A2
    nsv7139284copy number variation1nstd232human GRCh37.p13 chr13: 25,945,521-25,945,572 , GRCh38.p12 chr13: 25,371,383-25,371,434 ATP8A2
    nsv7139092copy number variation1nstd232human GRCh37.p13 chr13: 26,102,892-26,102,983 , GRCh38.p12 chr13: 25,528,754-25,528,845 ATP8A2
    nsv7094071copy number variation1nstd102humanUncertain significance GRCh37 chr13: 26,586,649-26,594,123 , GRCh38.p12 chr13: 26,012,511-26,019,985 ATP8A2
    nsv7093994copy number variation1nstd102humanPathogenic GRCh37 chr13: 24,293,859-26,594,123 , GRCh38.p12 chr13: 23,719,720-26,019,985 IRX1P1, MTCO3P2, 54 more genes
    nsv7067312inversion1nstd229human GRCh38 chr13: 25,371,681-25,371,755 , GRCh37.p13 chr13: 25,945,819-25,945,893 ATP8A2
    nsv7067130inversion1nstd229human GRCh38 chr13: 25,516,229-25,516,330 , GRCh37.p13 chr13: 26,090,367-26,090,468 ATP8A2, RNU6-78P
    nsv7063923inversion1nstd229human GRCh38 chr13: 25,434,345-25,438,658 , GRCh37.p13 chr13: 26,008,483-26,012,796 ATP8A2
    nsv7063835inversion1nstd229human GRCh38 chr13: 22,751,036-26,757,157 , GRCh37.p13 chr13: 23,325,175-27,331,294 SPATA13, LOC105370122, 86 more genes
    nsv7061791inversion1nstd229human GRCh38 chr13: 25,577,075-25,577,186 , GRCh37.p13 chr13: 26,151,213-26,151,324 ATP8A2
    nsv7060251inversion1nstd229human GRCh38 chr13: 25,415,347-25,415,436 , GRCh37.p13 chr13: 25,989,485-25,989,574 ATP8A2
    nsv6937922copy number variation1nstd229human GRCh38 chr13: 25,450,651-25,451,879 , GRCh37.p13 chr13: 26,024,789-26,026,017 ATP8A2
    nsv6937802copy number variation1nstd229human GRCh38 chr13: 25,404,276-25,406,764 , GRCh37.p13 chr13: 25,978,414-25,980,902 ATP8A2
    nsv6937601copy number variation1nstd229human GRCh38 chr13: 25,875,229-25,875,744 , GRCh37.p13 chr13: 26,449,367-26,449,882 ATP8A2
    nsv6937484copy number variation1nstd229human GRCh38 chr13: 25,856,217-25,858,924 , GRCh37.p13 chr13: 26,430,355-26,433,062 ATP8A2
    nsv6937368copy number variation1nstd229human GRCh38 chr13: 26,018,649-26,037,703 , GRCh37.p13 chr13: 26,592,787-26,611,841 ATP8A2
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