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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5945794copy number variation1nstd209human GRCh38 chr18: 36,827,967-36,830,082 , GRCh37.p13 chr18: 34,407,930-34,410,045 TPGS2, KIAA1328
    nsv5934663copy number variation1nstd209human GRCh38 chr18: 36,806,934-36,807,015 , GRCh37.p13 chr18: 34,386,897-34,386,978 TPGS2
    nsv5876496copy number variation1nstd209human GRCh38 chr18: 36,828,015-36,830,255 , GRCh37.p13 chr18: 34,407,978-34,410,218 KIAA1328, TPGS2
    nsv5531688copy number variation1nstd206human GRCh38 chr18: 36,535,152-36,872,753 , GRCh37.p13 chr18: 34,115,115-34,452,716 TPGS2, KIAA1328, 2 more genes
    nsv5524276copy number variation1nstd206human GRCh38 chr18: 36,806,936-36,807,016 , GRCh37.p13 chr18: 34,386,899-34,386,979 TPGS2
    nsv5519248copy number variation1nstd206human GRCh38 chr18: 36,827,994-36,830,083 , GRCh37.p13 chr18: 34,407,957-34,410,046 TPGS2, KIAA1328
    nsv5375169translocation1nstd200human GRCh38 chr18: 36,817,872-36,817,872 , GRCh38 chr18: 36,816,103-36,816,103 , GRCh37.p13 chr18: 34,397,835-34,397,835 , GRCh37.p13 chr18: 34,396,066-34,396,066 TPGS2
    nsv5343936translocation1nstd200human GRCh37 chr18: 34,396,066-34,396,066 , GRCh37 chr18: 34,397,835-34,397,835 , GRCh38.p12 chr18: 36,816,103-36,816,103 , GRCh38.p12 chr18: 36,817,872-36,817,872 TPGS2
    nsv5146869mobile element insertion1nstd203human GRCh38 chr18: 36,823,460-36,823,510 , GRCh37.p13 chr18: 34,403,423-34,403,473 TPGS2
    nsv5142136mobile element insertion1nstd203human GRCh38 chr18: 36,802,634-36,802,646 , GRCh37.p13 chr18: 34,382,597-34,382,609 TPGS2
    nsv5024104copy number variation1nstd200human GRCh38 chr18: 36,697,411-37,380,131 , GRCh37.p13 chr18: 34,277,374-34,960,094 TPGS2, CELF4, 4 more genes
    nsv5024103copy number variation1nstd200human GRCh38 chr18: 36,697,290-37,375,435 , GRCh37.p13 chr18: 34,277,253-34,955,398 TPGS2, CELF4, 4 more genes
    nsv5024102copy number variation1nstd200human GRCh38 chr18: 36,628,922-37,334,384 , GRCh37.p13 chr18: 34,208,885-34,914,347 KIAA1328, LOC105372069, 5 more genes
    nsv5011381copy number variation1nstd200human GRCh38 chr18: 36,828,409-36,943,546 , GRCh37.p13 chr18: 34,408,372-34,523,509 TPGS2, KIAA1328, 1 more genes
    nsv5011380copy number variation1nstd200human GRCh38 chr18: 36,825,449-36,827,188 , GRCh37.p13 chr18: 34,405,412-34,407,151 TPGS2, KIAA1328
    nsv5011379copy number variation1nstd200human GRCh38 chr18: 36,800,888-36,802,776 , GRCh37.p13 chr18: 34,380,851-34,382,739 TPGS2
    nsv5011378copy number variation1nstd200human GRCh38 chr18: 36,785,182-36,791,509 , GRCh37.p13 chr18: 34,365,145-34,371,472 TPGS2
    nsv5011377copy number variation1nstd200human GRCh38 chr18: 36,782,899-36,788,171 , GRCh37.p13 chr18: 34,362,862-34,368,134 TPGS2
    nsv4859280copy number variation1nstd200human GRCh37 chr18: 34,405,412-34,407,151 , GRCh38.p12 chr18: 36,825,449-36,827,188 KIAA1328, TPGS2
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