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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7056555inversion1nstd229human GRCh38 chr5: 39,192,895-39,199,791 , GRCh37.p13 chr5: 39,192,997-39,199,893 FYB1
    nsv7050412inversion1nstd229human GRCh38 chr5: 39,205,460-39,205,518 , GRCh37.p13 chr5: 39,205,562-39,205,620 FYB1
    nsv6777116copy number variation1nstd229human GRCh38 chr5: 39,134,301-39,225,800 , GRCh37.p13 chr5: 39,134,403-39,225,902 GOLGA5P1, FYB1
    nsv6776008copy number variation1nstd229human GRCh38 chr5: 39,241,305-39,253,954 , GRCh37.p13 chr5: 39,241,407-39,254,056 FYB1
    nsv6774840copy number variation1nstd229human GRCh38 chr5: 39,140,593-39,142,259 , GRCh37.p13 chr5: 39,140,695-39,142,361 FYB1
    nsv6774608copy number variation1nstd229human GRCh38 chr5: 39,254,377-39,255,164 , GRCh37.p13 chr5: 39,254,479-39,255,266 FYB1
    nsv6774321copy number variation1nstd229human GRCh38 chr5: 39,160,953-39,201,512 , GRCh37.p13 chr5: 39,161,055-39,201,614 GOLGA5P1, FYB1
    nsv6772741copy number variation1nstd229human GRCh38 chr5: 39,253,353-39,254,048 , GRCh37.p13 chr5: 39,253,455-39,254,150 FYB1
    nsv6772508copy number variation1nstd229human GRCh38 chr5: 39,240,588-39,240,772 , GRCh37.p13 chr5: 39,240,690-39,240,874 FYB1
    nsv6771288copy number variation1nstd229human GRCh38 chr5: 39,195,468-39,195,699 , GRCh37.p13 chr5: 39,195,570-39,195,801 FYB1
    nsv6770614copy number variation1nstd229human GRCh38 chr5: 39,238,746-39,252,788 , GRCh37.p13 chr5: 39,238,848-39,252,890 FYB1
    nsv6769429copy number variation1nstd229human GRCh38 chr5: 35,077,787-40,637,192 , GRCh37.p13 chr5: 35,077,889-40,637,294 LINC02110, LOC105374735, 68 more genes
    nsv6769256copy number variation1nstd229human GRCh38 chr5: 39,170,045-39,179,906 , GRCh37.p13 chr5: 39,170,147-39,180,008 FYB1, GOLGA5P1
    nsv6768757copy number variation1nstd229human GRCh38 chr5: 39,223,213-39,223,539 , GRCh37.p13 chr5: 39,223,315-39,223,641 FYB1
    nsv6768671copy number variation1nstd229human GRCh38 chr5: 39,218,675-39,228,051 , GRCh37.p13 chr5: 39,218,777-39,228,153 FYB1
    nsv6768319copy number variation1nstd229human GRCh38 chr5: 39,204,230-39,205,806 , GRCh37.p13 chr5: 39,204,332-39,205,908 FYB1
    nsv6767994copy number variation1nstd229human GRCh38 chr5: 39,137,716-39,143,913 , GRCh37.p13 chr5: 39,137,818-39,144,015 FYB1
    nsv6767964copy number variation1nstd229human GRCh38 chr5: 39,249,976-39,254,336 , GRCh37.p13 chr5: 39,250,078-39,254,438 FYB1
    nsv6766717copy number variation1nstd229human GRCh38 chr5: 39,251,001-39,253,300 , GRCh37.p13 chr5: 39,251,103-39,253,402 FYB1
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