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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112732copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,200-4,012,072 , GRCh38.p12 chr5: 13,200-4,011,958 SLC9A3-AS1, LOC107984098, 76 more genes
    nsv5892539copy number variation1nstd209human GRCh38 chr5: 2,712,601-2,715,235 , GRCh37.p13 chr5: 2,712,715-2,715,349 LSINCT5, IRX2
    nsv5842660copy number variation1nstd209human GRCh38 chr5: 2,736,756-2,738,796 , GRCh37.p13 chr5: 2,736,870-2,738,910 IRX2
    nsv5842337copy number variation1nstd209human GRCh38 chr5: 2,712,563-2,715,236 , GRCh37.p13 chr5: 2,712,677-2,715,350 IRX2, LSINCT5
    nsv5720279mobile element insertion1nstd211human GRCh38 chr5: 2,747,023-2,747,023 , GRCh37.p13 chr5: 2,747,137-2,747,137 IRX2
    nsv5632671insertion1nstd207human GRCh38 chr5: 2,706,070-2,706,070 , GRCh37.p13 chr5: 2,706,184-2,706,184 IRX2
    nsv5559635mobile element insertion1nstd206human GRCh38 chr5: 2,747,039-2,747,074 , GRCh37.p13 chr5: 2,747,153-2,747,188 IRX2
    nsv5473634copy number variation1nstd206human GRCh38 chr5: 2,732,944-2,733,136 , GRCh37.p13 chr5: 2,733,058-2,733,250 IRX2
    nsv5467166copy number variation1nstd206human GRCh38 chr5: 2,712,602-2,715,236 , GRCh37.p13 chr5: 2,712,716-2,715,350 LSINCT5, IRX2
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5377823translocation1nstd200human GRCh38 chr5: 2,715,236-2,715,236 , GRCh38 chr5: 2,712,602-2,712,602 , GRCh37.p13 chr5: 2,715,350-2,715,350 , GRCh37.p13 chr5: 2,712,716-2,712,716 LSINCT5, IRX2
    nsv5367991translocation1nstd200human GRCh38 chr18: 23,771,461-23,771,461 , GRCh38 chr5: 2,751,434-2,751,434 , GRCh37.p13 chr18: 21,351,425-21,351,425 , GRCh37.p13 chr5: 2,751,548-2,751,548 LAMA3, IRX2-DT, 1 more genes
    nsv5367990translocation1nstd200human GRCh38 chr5: 2,711,168-2,711,168 , GRCh38 chr5: 2,713,712-2,713,712 , GRCh37.p13 chr5: 2,713,826-2,713,826 , GRCh37.p13 chr5: 2,711,282-2,711,282 IRX2, LSINCT5
    nsv5367989translocation1nstd200human GRCh38 chr5: 2,709,690-2,709,690 , GRCh38 chr5: 2,711,432-2,711,432 , GRCh37.p13 chr5: 2,709,804-2,709,804 , GRCh37.p13 chr5: 2,711,546-2,711,546 IRX2, LSINCT5
    nsv5335461translocation1nstd200human GRCh37 chr5: 2,751,548-2,751,548 , GRCh37 chr18: 21,351,425-21,351,425 , GRCh38.p12 chr18: 23,771,461-23,771,461 , GRCh38.p12 chr5: 2,751,434-2,751,434 LAMA3, IRX2-DT, 1 more genes
    nsv5330673translocation1nstd200human GRCh37 chr5: 2,712,716-2,712,716 , GRCh37 chr5: 2,715,350-2,715,350 , GRCh38.p12 chr5: 2,712,602-2,712,602 , GRCh38.p12 chr5: 2,715,236-2,715,236 LSINCT5, IRX2
    nsv5308200copy number variation1nstd204human GRCh38.p13 chr5: 2,740,607-2,740,950 , GRCh37.p13 chr5: 2,740,721-2,741,064 IRX2
    nsv5091375mobile element insertion1nstd203human GRCh38 chr5: 2,706,937-2,706,952 , GRCh37.p13 chr5: 2,707,051-2,707,066 IRX2
    nsv4936833copy number variation1nstd200human GRCh38 chr5: 2,739,007-2,739,082 , GRCh37.p13 chr5: 2,739,121-2,739,196 IRX2
    nsv4936832copy number variation1nstd200human GRCh38 chr5: 2,724,886-2,726,309 , GRCh37.p13 chr5: 2,725,000-2,726,423 IRX2
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