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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892600copy number variation1nstd209human GRCh38 chr5: 115,654,880-115,654,952 , GRCh37.p13 chr5: 114,990,577-114,990,649 LOC102467217
    nsv5685313mobile element insertion2nstd211human GRCh38 chr5: 115,667,374-115,667,374 , GRCh37.p13 chr5: 115,003,071-115,003,071 LOC102467217
    nsv5683513mobile element insertion2nstd211human GRCh38 chr5: 115,662,997-115,662,997 , GRCh37.p13 chr5: 114,998,694-114,998,694 LOC102467217
    nsv5569677copy number variation1nstd207human GRCh38 chr5: 115,654,880-115,654,952 , GRCh37.p13 chr5: 114,990,577-114,990,649 LOC102467217
    nsv5465344copy number variation1nstd206human GRCh38 chr5: 115,663,288-115,663,411 , GRCh37.p13 chr5: 114,998,985-114,999,108 LOC102467217
    nsv5456936copy number variation1nstd206human GRCh38 chr5: 115,666,061-115,666,162 , GRCh37.p13 chr5: 115,001,758-115,001,859 LOC102467217
    nsv5411840mobile element insertion1nstd206human GRCh38 chr5: 115,662,997-115,663,048 , GRCh37.p13 chr5: 114,998,694-114,998,745 LOC102467217
    nsv5401045mobile element insertion1nstd206human GRCh38 chr5: 115,667,374-115,667,425 , GRCh37.p13 chr5: 115,003,071-115,003,122 LOC102467217
    nsv5093637mobile element insertion1nstd203human GRCh38 chr5: 115,662,984-115,662,997 , GRCh37.p13 chr5: 114,998,681-114,998,694 LOC102467217
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4734597copy number variation1nstd199human GRCh37 chr5: 114,990,520-114,990,593 , GRCh38.p12 chr5: 115,654,823-115,654,896 LOC102467217
    nsv4642685copy number variation1nstd186human GRCh37 chr5: 114,990,579-114,990,650 , GRCh38.p12 chr5: 115,654,882-115,654,953 LOC102467217
    nsv4491675mobile element insertion1nstd166human GRCh37.p13 chr5: 114,998,681-114,998,681 , GRCh38.p12 chr5: 115,662,984-115,662,984 LOC102467217
    nsv4456071copy number variation1nstd102humanPathogenic GRCh37 chr5: 108,304,806-121,335,239 , GRCh38.p12 chr5: 108,969,105-121,999,544 HMGN1P13, LOC101927023, 153 more genes
    nsv4455983copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762 LOC345576, LOC107986436, 419 more genes
    nsv4442832copy number variation1nstd175human GRCh37 chr5: 114,990,577-114,990,650 , GRCh38.p12 chr5: 115,654,880-115,654,953 LOC102467217
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