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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6776476copy number variation1nstd229human GRCh38 chr5: 35,672,999-35,673,905 , GRCh37.p13 chr5: 35,673,101-35,674,007 SPEF2
    nsv6774564copy number variation1nstd229human GRCh38 chr5: 35,704,636-35,710,441 , GRCh37.p13 chr5: 35,704,738-35,710,543 LOC105374724, SPEF2
    nsv6773838copy number variation1nstd229human GRCh38 chr5: 35,732,153-35,740,130 , GRCh37.p13 chr5: 35,732,255-35,740,232 LOC105374724, SPEF2
    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
    nsv6769406copy number variation1nstd229human GRCh38 chr5: 35,648,198-35,654,228 , GRCh37.p13 chr5: 35,648,300-35,654,330 SPEF2
    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
    nsv6764798copy number variation1nstd229human GRCh38 chr5: 35,734,401-35,734,440 , GRCh37.p13 chr5: 35,734,503-35,734,542 SPEF2, LOC105374724
    nsv6764727copy number variation1nstd229human GRCh38 chr5: 35,755,069-35,758,930 , GRCh37.p13 chr5: 35,755,171-35,759,032 SPEF2, LOC105374724
    nsv6764335copy number variation1nstd229human GRCh38 chr5: 35,781,701-35,790,500 , GRCh37.p13 chr5: 35,781,803-35,790,602 SPEF2, LOC105374724
    nsv6764175copy number variation1nstd229human GRCh38 chr5: 35,769,997-35,770,030 , GRCh37.p13 chr5: 35,770,099-35,770,132 LOC105374724, SPEF2
    nsv6764056copy number variation1nstd229human GRCh38 chr5: 35,678,625-35,678,764 , GRCh37.p13 chr5: 35,678,727-35,678,866 LOC105374724, SPEF2
    nsv6763146copy number variation1nstd229human GRCh38 chr5: 35,701,460-35,703,003 , GRCh37.p13 chr5: 35,701,562-35,703,105 SPEF2, LOC105374724
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