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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5952984insertion1nstd209human GRCh38 chr8: 42,880,945-42,880,945 , GRCh37.p13 chr8: 42,736,088-42,736,088 RNF170, RN7SL806P
    nsv5925348copy number variation1nstd209human GRCh38 chr8: 42,880,509-42,887,029 , GRCh37.p13 chr8: 42,735,652-42,742,172 RNF170, RN7SL806P
    nsv5921507copy number variation1nstd209human GRCh38 chr8: 42,896,841-42,896,891 , GRCh37.p13 chr8: 42,751,984-42,752,034 RNF170, HOOK3
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5912811copy number variation1nstd209human GRCh38 chr8: 42,895,979-42,896,123 , GRCh37.p13 chr8: 42,751,122-42,751,266 RNF170, HOOK3, 1 more genes
    nsv5851300copy number variation1nstd209human GRCh38 chr8: 42,880,588-42,886,770 , GRCh37.p13 chr8: 42,735,731-42,741,913 RN7SL806P, RNF170
    nsv5700983mobile element insertion2nstd211human GRCh38 chr8: 42,880,957-42,880,957 , GRCh37.p13 chr8: 42,736,100-42,736,100 RN7SL806P, RNF170
    nsv5624605insertion1nstd207human GRCh38 chr8: 42,884,900-42,884,900 , GRCh37.p13 chr8: 42,740,043-42,740,043 RNF170
    nsv5492711copy number variation1nstd206human GRCh38 chr8: 42,895,979-42,896,127 , GRCh37.p13 chr8: 42,751,122-42,751,270 RNF170, HOOK3, 1 more genes
    nsv5478583copy number variation1nstd206human GRCh38 chr8: 42,880,490-42,887,060 , GRCh37.p13 chr8: 42,735,633-42,742,203 RN7SL806P, RNF170
    nsv5477172copy number variation1nstd206human GRCh38 chr8: 42,894,440-42,894,507 , GRCh37.p13 chr8: 42,749,583-42,749,650 RNF170, MIR4469
    nsv5412340mobile element insertion1nstd206human GRCh38 chr8: 42,880,957-42,881,008 , GRCh37.p13 chr8: 42,736,100-42,736,151 RN7SL806P, RNF170
    nsv5364153translocation1nstd200human GRCh38 chr8: 42,895,979-42,895,979 , GRCh38 chr8: 42,896,127-42,896,127 , GRCh37.p13 chr8: 42,751,122-42,751,122 , GRCh37.p13 chr8: 42,751,270-42,751,270 RNF170, HOOK3, 1 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5189365mobile element insertion1nstd203human GRCh38 chr8: 42,890,260-42,890,295 , GRCh37.p13 chr8: 42,745,403-42,745,438 RNF170
    nsv5119697mobile element insertion1nstd203human GRCh38 chr8: 42,884,874-42,884,900 , GRCh37.p13 chr8: 42,740,017-42,740,043 RNF170
    nsv5118938mobile element insertion1nstd203human GRCh38 chr8: 42,884,845-42,884,900 , GRCh37.p13 chr8: 42,739,988-42,740,043 RNF170
    nsv5118616mobile element insertion1nstd203human GRCh38 chr8: 42,884,857-42,884,900 , GRCh37.p13 chr8: 42,740,000-42,740,043 RNF170
    nsv5118437mobile element insertion1nstd203human GRCh38 chr8: 42,884,853-42,884,900 , GRCh37.p13 chr8: 42,739,996-42,740,043 RNF170
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