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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902747copy number variation1nstd209human GRCh38 chr3: 27,474,186-27,475,833 , GRCh37.p13 chr3: 27,515,677-27,517,324 SLC4A7
    nsv5899785copy number variation1nstd209human GRCh38 chr3: 26,482,972-28,493,095 , GRCh37.p13 chr3: 26,524,463-28,534,586 , MICOS10P3, 24 more genes
    nsv5898672copy number variation1nstd209human GRCh38 chr3: 27,388,826-27,388,923 , GRCh37.p13 chr3: 27,430,317-27,430,414 SLC4A7
    nsv5835896copy number variation1nstd209human GRCh38 chr3: 27,474,086-27,476,035 , GRCh37.p13 chr3: 27,515,577-27,517,526 SLC4A7
    nsv5675763mobile element insertion1nstd211human GRCh38 chr3: 27,404,683-27,404,683 , GRCh37.p13 chr3: 27,446,174-27,446,174 SLC4A7
    nsv5575628copy number variation1nstd207human GRCh38 chr3: 27,388,838-27,388,931 , GRCh37.p13 chr3: 27,430,329-27,430,422 SLC4A7
    nsv5449572copy number variation1nstd206human GRCh38 chr3: 27,419,534-27,419,604 , GRCh37.p13 chr3: 27,461,025-27,461,095 SLC4A7
    nsv5445827copy number variation1nstd206human GRCh38 chr3: 26,982,564-27,388,155 , GRCh37.p13 chr3: 27,024,055-27,429,646 , MICOS10P3, 3 more genes
    nsv5444633copy number variation1nstd206human GRCh38 chr3: 27,474,188-27,475,834 , GRCh37.p13 chr3: 27,515,679-27,517,325 SLC4A7
    nsv5441884copy number variation1nstd206human GRCh38 chr3: 27,388,822-27,388,942 , GRCh37.p13 chr3: 27,430,313-27,430,433 SLC4A7
    nsv5438858copy number variation1nstd206human GRCh38 chr3: 27,466,204-27,468,980 , GRCh37.p13 chr3: 27,507,695-27,510,471 SLC4A7
    nsv5399867mobile element insertion1nstd206human GRCh38 chr3: 27,404,683-27,404,734 , GRCh37.p13 chr3: 27,446,174-27,446,225 SLC4A7
    nsv5377390translocation1nstd200human GRCh38 chr3: 27,472,252-27,472,252 , GRCh38 chr3: 27,465,954-27,465,954 , GRCh37.p13 chr3: 27,507,445-27,507,445 , GRCh37.p13 chr3: 27,513,743-27,513,743 SLC4A7
    nsv5377389translocation1nstd200human GRCh38 chr3: 27,476,981-27,476,981 , GRCh38 chr3: 27,465,794-27,465,794 , GRCh37.p13 chr3: 27,507,285-27,507,285 , GRCh37.p13 chr3: 27,518,472-27,518,472 SLC4A7
    nsv5333341translocation1nstd200human GRCh37 chr3: 27,507,285-27,507,285 , GRCh37 chr3: 27,518,472-27,518,472 , GRCh38.p12 chr3: 27,476,981-27,476,981 , GRCh38.p12 chr3: 27,465,794-27,465,794 SLC4A7
    nsv5314892copy number variation1nstd204human GRCh38.p13 chr3: 27,388,822-27,388,942 , GRCh37.p13 chr3: 27,430,313-27,430,433 SLC4A7
    nsv5218850copy number variation1nstd204human GRCh38.p13 chr3: 27,373,201-27,376,400 , GRCh37.p13 chr3: 27,414,692-27,417,891 SLC4A7
    nsv5079281mobile element insertion1nstd203human GRCh38 chr3: 27,458,543-27,458,553 , GRCh37.p13 chr3: 27,500,034-27,500,044 SLC4A7
    nsv5067693mobile element insertion1nstd203human GRCh38 chr3: 27,464,541-27,464,560 , GRCh37.p13 chr3: 27,506,032-27,506,051 SLC4A7
    nsv5063765mobile element insertion1nstd203human GRCh38 chr3: 27,460,801-27,460,816 , GRCh37.p13 chr3: 27,502,292-27,502,307 RPS20P15, SLC4A7
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