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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123814copy number variation1nstd186human GRCh37 chr20: 54,963,149-54,963,210 , GRCh38.p12 chr20: 56,388,093-56,388,154 AURKA
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5948579copy number variation1nstd209human GRCh38 chr20: 56,388,093-56,388,153 , GRCh37.p13 chr20: 54,963,149-54,963,209 AURKA
    nsv5710782mobile element insertion1nstd211human GRCh38 chr20: 56,384,071-56,384,071 , GRCh37.p13 chr20: 54,959,127-54,959,127 AURKA
    nsv5695022mobile element insertion1nstd211human GRCh38 chr20: 56,375,566-56,375,566 , GRCh37.p13 chr20: 54,950,622-54,950,622 AURKA
    nsv5667696insertion1nstd207human GRCh38 chr20: 56,388,093-56,388,093 , GRCh37.p13 chr20: 54,963,149-54,963,149 AURKA
    nsv5532564copy number variation1nstd206human GRCh38 chr20: 56,388,093-56,388,154 , GRCh37.p13 chr20: 54,963,149-54,963,210 AURKA
    nsv5522873copy number variation1nstd206human GRCh38 chr20: 56,379,819-56,380,212 , GRCh37.p13 chr20: 54,954,875-54,955,268 AURKA
    nsv5428431mobile element insertion1nstd206human GRCh38 chr20: 56,375,566-56,375,617 , GRCh37.p13 chr20: 54,950,622-54,950,673 AURKA
    nsv5419370mobile element insertion1nstd206human GRCh38 chr20: 56,384,071-56,384,122 , GRCh37.p13 chr20: 54,959,127-54,959,178 AURKA
    nsv5166590mobile element insertion1nstd203human GRCh38 chr20: 56,375,553-56,375,566 , GRCh37.p13 chr20: 54,950,609-54,950,622 AURKA
    nsv5013292copy number variation1nstd200human GRCh38 chr20: 56,380,469-56,380,567 , GRCh37.p13 chr20: 54,955,525-54,955,623 AURKA
    nsv4853980copy number variation1nstd200human GRCh37 chr20: 54,963,599-54,964,519 , GRCh38.p12 chr20: 56,388,543-56,389,463 AURKA
    nsv4752339insertion1nstd199human GRCh37 chr20: 54,963,182-54,963,182 , GRCh38.p12 chr20: 56,388,126-56,388,126 AURKA
    nsv4563057insertion1nstd166human GRCh37.p13 chr20: 54,950,609-54,950,609 , GRCh38.p12 chr20: 56,375,553-56,375,553 AURKA
    nsv4444211insertion1nstd175human GRCh37 chr20: 54,963,149-54,963,149 , GRCh38.p12 chr20: 56,388,093-56,388,093 AURKA
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4290085copy number variation1nstd166human GRCh37.p13 chr20: 54,964,000-54,969,000 , GRCh38.p12 chr20: 56,388,944-56,393,944 AURKA, CSTF1
    nsv3939187insertion1nstd167human GRCh37 chr20: 54,963,149-54,963,149 , GRCh38.p12 chr20: 56,388,093-56,388,093 AURKA
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
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