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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139822insertion1nstd232human GRCh37.p13 chr18: 28,730,336-28,730,336 , GRCh38.p12 chr18: 31,150,373-31,150,373 DSC1, DSCAS
    nsv7095440copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,647,981-29,648,347 , GRCh38.p12 chr18: 31,068,015-32,068,384 RNU6-167P, LOC390846, 22 more genes
    nsv7074645inversion1nstd229human GRCh38 chr18: 30,537,670-35,063,371 , GRCh37.p13 chr18: 28,117,636-32,643,335 DSC1, RN7SKP44, 46 more genes
    nsv7014620copy number variation1nstd229human GRCh38 chr18: 31,150,001-31,160,000 , GRCh37.p13 chr18: 28,729,964-28,739,963 DSC1, DSCAS
    nsv7012956copy number variation1nstd229human GRCh38 chr18: 31,134,786-31,139,747 , GRCh37.p13 chr18: 28,714,749-28,719,710 DSC1, DSCAS
    nsv7011839copy number variation1nstd229human GRCh38 chr18: 29,648,720-31,204,673 , GRCh37.p13 chr18: 27,228,685-28,784,636 LOC105372045, DSC2, 7 more genes
    nsv7010823copy number variation1nstd229human GRCh38 chr18: 31,149,984-31,153,150 , GRCh37.p13 chr18: 28,729,947-28,733,113 DSCAS, DSC1
    nsv7010714copy number variation1nstd229human GRCh38 chr18: 31,129,196-31,137,145 , GRCh37.p13 chr18: 28,709,159-28,717,108 DSCAS, DSC1
    nsv7010545copy number variation1nstd229human GRCh38 chr18: 31,113,220-31,263,304 , GRCh37.p13 chr18: 28,693,183-28,843,267 DSCAS, LOC105372049, 1 more genes
    nsv7005387copy number variation1nstd229human GRCh38 chr18: 31,146,201-31,196,900 , GRCh37.p13 chr18: 28,726,164-28,776,863 DSC1, DSCAS
    nsv6624582copy number variation1nstd224human GRCh37 chr18: 28,597,270-29,027,889 , GRCh38.p12 chr18: 31,017,304-31,447,926 DSC1, DSG4, 8 more genes
    nsv6534270copy number variation1nstd223human GRCh38 chr18: 29,648,720-31,204,673 , GRCh37.p13 chr18: 27,228,685-28,784,636 DSC2, DSCAS, 7 more genes
    nsv6533366copy number variation1nstd223human GRCh38 chr18: 31,146,981-31,147,376 , GRCh37.p13 chr18: 28,726,944-28,727,339 DSCAS, DSC1
    nsv6531500copy number variation1nstd223human GRCh38 chr18: 31,134,114-31,134,703 , GRCh37.p13 chr18: 28,714,077-28,714,666 DSCAS, DSC1
    nsv6520965copy number variation1nstd223human GRCh38 chr18: 31,139,107-31,139,553 , GRCh37.p13 chr18: 28,719,070-28,719,516 DSCAS, DSC1
    nsv6520675copy number variation1nstd223human GRCh38 chr18: 31,131,234-31,131,572 , GRCh37.p13 chr18: 28,711,197-28,711,535 DSCAS, DSC1
    nsv6519821copy number variation1nstd223human GRCh38 chr18: 31,129,194-31,137,144 , GRCh37.p13 chr18: 28,709,157-28,717,107 DSC1, DSCAS
    nsv6519475copy number variation1nstd223human GRCh38 chr18: 31,150,046-31,150,377 , GRCh37.p13 chr18: 28,730,009-28,730,340 DSC1, DSCAS
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
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