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Items: 1 to 20 of 751

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144428copy number variation1nstd232human GRCh37.p13 chr5: 35,841,809-35,841,924 , GRCh38.p12 chr5: 35,841,707-35,841,822 LOC105374724
    nsv7143989copy number variation1nstd232human GRCh37.p13 chr5: 35,841,918-35,841,977 , GRCh38.p12 chr5: 35,841,816-35,841,875 LOC105374724
    nsv7141724copy number variation1nstd232human GRCh37.p13 chr5: 35,841,819-35,841,873 , GRCh38.p12 chr5: 35,841,717-35,841,771 LOC105374724
    nsv7141034insertion1nstd232human GRCh37.p13 chr5: 35,752,764-35,752,764 , GRCh38.p12 chr5: 35,752,662-35,752,662 SPEF2, LOC105374724
    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
    nsv7048789inversion1nstd229human GRCh38 chr5: 35,602,363-36,053,738 , GRCh37.p13 chr5: 35,602,465-36,053,840 UGT3A1, RNU7-130P, 6 more genes
    nsv7043378inversion1nstd229human GRCh38 chr5: 35,626,440-35,717,987 , GRCh37.p13 chr5: 35,626,542-35,718,089 SPEF2, RNU7-130P, 1 more genes
    nsv7042420inversion1nstd229human GRCh38 chr5: 35,853,711-35,866,637 , GRCh37.p13 chr5: 35,853,813-35,866,739 LOC105374724, IL7R
    nsv7040914inversion1nstd229human GRCh38 chr5: 35,814,297-35,814,375 , GRCh37.p13 chr5: 35,814,399-35,814,477 SPEF2, LOC105374724
    nsv7040503inversion1nstd229human GRCh38 chr5: 35,751,076-35,751,634 , GRCh37.p13 chr5: 35,751,178-35,751,736 SPEF2, LOC105374724
    nsv6775305copy number variation1nstd229human GRCh38 chr5: 35,859,916-35,869,694 , GRCh37.p13 chr5: 35,860,018-35,869,796 LOC105374724, IL7R
    nsv6774890copy number variation1nstd229human GRCh38 chr5: 35,823,934-35,828,366 , GRCh37.p13 chr5: 35,824,036-35,828,468 LOC105374724
    nsv6774564copy number variation1nstd229human GRCh38 chr5: 35,704,636-35,710,441 , GRCh37.p13 chr5: 35,704,738-35,710,543 LOC105374724, SPEF2
    nsv6773877copy number variation1nstd229human GRCh38 chr5: 35,858,003-35,871,531 , GRCh37.p13 chr5: 35,858,105-35,871,633 IL7R, LOC105374724
    nsv6773838copy number variation1nstd229human GRCh38 chr5: 35,732,153-35,740,130 , GRCh37.p13 chr5: 35,732,255-35,740,232 LOC105374724, SPEF2
    nsv6771792copy number variation1nstd229human GRCh38 chr5: 35,837,895-35,842,307 , GRCh37.p13 chr5: 35,837,997-35,842,409 LOC105374724
    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
    nsv6767728copy number variation1nstd229human GRCh38 chr5: 35,687,952-35,703,887 , GRCh37.p13 chr5: 35,688,054-35,703,989 SPEF2, LOC105374724
    nsv6764861copy number variation1nstd229human GRCh38 chr5: 35,753,000-35,841,477 , GRCh37.p13 chr5: 35,753,102-35,841,579 LOC105374724, SPEF2
    nsv6764801copy number variation1nstd229human GRCh38 chr5: 35,654,592-35,732,876 , GRCh37.p13 chr5: 35,654,694-35,732,978 SPEF2, LOC105374724
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