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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923694copy number variation1nstd209human GRCh38 chr8: 102,231,589-102,231,721 , GRCh37.p13 chr8: 103,243,817-103,243,949 RRM2B
    nsv5922376copy number variation1nstd209human GRCh38 chr8: 102,209,351-102,209,474 , GRCh37.p13 chr8: 103,221,579-103,221,702 RRM2B
    nsv5909893copy number variation1nstd209human GRCh38 chr8: 102,239,105-102,239,332 , GRCh37.p13 chr8: 103,251,333-103,251,560 UBR5-DT, RRM2B
    nsv5908095copy number variation1nstd209human GRCh38 chr8: 102,234,648-102,235,360 , GRCh37.p13 chr8: 103,246,876-103,247,588 RRM2B
    nsv5541673insertion1nstd206human GRCh38 chr8: 102,220,100-102,220,135 , GRCh37.p13 chr8: 103,232,328-103,232,363 RRM2B
    nsv5487611copy number variation1nstd206human GRCh38 chr8: 102,200,979-102,319,280 , GRCh37.p13 chr8: 103,213,207-103,331,508 UBR5, SUMO2P19, 2 more genes
    nsv5483102copy number variation1nstd206human GRCh38 chr8: 102,209,352-102,209,475 , GRCh37.p13 chr8: 103,221,580-103,221,703 RRM2B
    nsv5372069translocation1nstd200human GRCh38 chr8: 102,239,219-102,239,219 , GRCh38 chr8: 102,239,138-102,239,138 , GRCh37.p13 chr8: 103,251,366-103,251,366 , GRCh37.p13 chr8: 103,251,447-103,251,447 UBR5-DT, RRM2B
    nsv5333826translocation1nstd200human GRCh37 chr8: 103,221,580-103,221,580 , GRCh37 chr8: 103,221,703-103,221,703 , GRCh38.p12 chr8: 102,209,352-102,209,352 , GRCh38.p12 chr8: 102,209,475-102,209,475 RRM2B
    nsv5333703translocation1nstd200human GRCh37 chr8: 103,251,366-103,251,366 , GRCh37 chr8: 103,251,447-103,251,447 , GRCh38.p12 chr8: 102,239,219-102,239,219 , GRCh38.p12 chr8: 102,239,138-102,239,138 UBR5-DT, RRM2B
    nsv5301036copy number variation1nstd204human GRCh38.p13 chr8: 102,226,506-102,371,281 , GRCh37.p13 chr8: 103,238,734-103,383,509 UBR5, SUMO2P19, 2 more genes
    nsv5252661copy number variation1nstd204human GRCh38.p13 chr8: 102,225,776-102,246,926 , GRCh37.p13 chr8: 103,238,004-103,259,154 UBR5-DT, RRM2B, 1 more genes
    nsv5116870mobile element insertion1nstd203human GRCh38 chr8: 102,220,084-102,220,100 , GRCh37.p13 chr8: 103,232,312-103,232,328 RRM2B
    nsv5110858mobile element insertion1nstd203human GRCh38 chr8: 102,214,753-102,214,753 , GRCh37.p13 chr8: 103,226,981-103,226,981 RRM2B
    nsv5107380mobile element insertion1nstd203human GRCh38 chr8: 102,215,944-102,215,944 , GRCh37.p13 chr8: 103,228,172-103,228,172 RRM2B
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4961573copy number variation1nstd200human GRCh38 chr8: 102,196,625-102,202,618 , GRCh37.p13 chr8: 103,208,853-103,214,846 RRM2B
    nsv4764725insertion1nstd199human GRCh37 chr8: 103,232,482-103,232,482 , GRCh38.p12 chr8: 102,220,254-102,220,254 RRM2B
    nsv4729735copy number variation1nstd102humanUncertain significance GRCh37 chr8: 103,152,797-103,408,155 , GRCh38.p12 chr8: 102,140,569-102,395,927 LOC112268018, RRM2B, 3 more genes
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