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Items: 1 to 20 of 949

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094391copy number variation1nstd102humanPathogenic GRCh37 chr15: 56,961,021-57,839,688 , GRCh38.p12 chr15: 56,668,823-57,547,490 ZNF280D, LOC107984759, 11 more genes
    nsv7094300copy number variation1nstd102humanPathogenic GRCh37 chr15: 57,458,580-57,545,686 , GRCh38.p12 chr15: 57,166,382-57,253,488 TCF12, HNRNPA3P11
    nsv7072381inversion1nstd229human GRCh38 chr15: 56,921,708-56,936,209 , GRCh37.p13 chr15: 57,213,906-57,228,407 TCF12
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv7069841inversion1nstd229human GRCh38 chr15: 55,108,583-62,405,114 , GRCh37.p13 chr15: 55,400,781-62,697,313 LOC105370834, RPL21P14, 118 more genes
    nsv7067196inversion1nstd229human GRCh38 chr15: 57,148,090-57,148,671 , GRCh37.p13 chr15: 57,440,288-57,440,869 TCF12
    nsv7063205inversion1nstd229human GRCh38 chr15: 57,199,292-57,199,359 , GRCh37.p13 chr15: 57,491,490-57,491,557 TCF12
    nsv6978074copy number variation1nstd229human GRCh38 chr15: 57,095,290-57,099,070 , GRCh37.p13 chr15: 57,387,488-57,391,268 TCF12
    nsv6977121copy number variation1nstd229human GRCh38 chr15: 56,974,535-56,989,436 , GRCh37.p13 chr15: 57,266,733-57,281,634 TCF12
    nsv6976712copy number variation1nstd229human GRCh38 chr15: 57,112,301-57,120,800 , GRCh37.p13 chr15: 57,404,499-57,412,998 TCF12
    nsv6975464copy number variation1nstd229human GRCh38 chr15: 56,954,301-56,955,600 , GRCh37.p13 chr15: 57,246,499-57,247,798 TCF12
    nsv6975431copy number variation1nstd229human GRCh38 chr15: 57,015,189-57,023,105 , GRCh37.p13 chr15: 57,307,387-57,315,303 TCF12
    nsv6975056copy number variation1nstd229human GRCh38 chr15: 56,950,007-56,950,595 , GRCh37.p13 chr15: 57,242,205-57,242,793 TCF12
    nsv6974617copy number variation1nstd229human GRCh38 chr15: 57,074,789-57,090,094 , GRCh37.p13 chr15: 57,366,987-57,382,292 TCF12
    nsv6974599copy number variation1nstd229human GRCh38 chr15: 56,957,788-56,965,491 , GRCh37.p13 chr15: 57,249,986-57,257,689 TCF12
    nsv6973845copy number variation1nstd229human GRCh38 chr15: 56,983,411-56,991,820 , GRCh37.p13 chr15: 57,275,609-57,284,018 TCF12
    nsv6973695copy number variation1nstd229human GRCh38 chr15: 57,031,583-57,032,017 , GRCh37.p13 chr15: 57,323,781-57,324,215 TCF12
    nsv6973431copy number variation1nstd229human GRCh38 chr15: 56,925,734-56,932,717 , GRCh37.p13 chr15: 57,217,932-57,224,915 TCF12
    nsv6973197copy number variation1nstd229human GRCh38 chr15: 57,011,397-57,016,812 , GRCh37.p13 chr15: 57,303,595-57,309,010 TCF12
    nsv6972927copy number variation1nstd229human GRCh38 chr15: 56,966,380-57,119,434 , GRCh37.p13 chr15: 57,258,578-57,411,632 TCF12
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