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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114647mobile element insertion1nstd186human GRCh37 chr18: 14,221,316-14,221,367 , GRCh38.p12 chr18: 14,221,317-14,221,368 RHOT1P1, ANKRD20A5P
    nsv5941968copy number variation1nstd209human GRCh38 chr18: 14,211,399-14,211,520 , GRCh37.p13 chr18: 14,211,398-14,211,519 ANKRD20A5P
    nsv5934975copy number variation1nstd209human GRCh38 chr18: 14,223,275-14,223,462 , GRCh37.p13 chr18: 14,223,274-14,223,461 ANKRD20A5P
    nsv5928972copy number variation1nstd209human GRCh38 chr18: 14,222,599-14,222,751 , GRCh37.p13 chr18: 14,222,598-14,222,750 ANKRD20A5P, RHOT1P1
    nsv5708232mobile element insertion2nstd211human GRCh38 chr18: 14,221,317-14,221,317 , GRCh37.p13 chr18: 14,221,316-14,221,316 ANKRD20A5P, RHOT1P1
    nsv5648145insertion1nstd207human GRCh38 chr18: 14,221,302-14,221,302 , GRCh37.p13 chr18: 14,221,301-14,221,301 ANKRD20A5P, RHOT1P1
    nsv5603747copy number variation1nstd207human GRCh38 chr18: 14,224,630-14,224,737 , GRCh37.p13 chr18: 14,224,629-14,224,736 ANKRD20A5P
    nsv5596386copy number variation1nstd207human GRCh38 chr18: 14,224,152-14,224,488 , GRCh37.p13 chr18: 14,224,151-14,224,487 ANKRD20A5P
    nsv5589967copy number variation1nstd207human GRCh38 chr18: 14,221,789-14,225,661 , GRCh37.p13 chr18: 14,221,788-14,225,660 ANKRD20A5P, RHOT1P1
    nsv5584876copy number variation1nstd207human GRCh38 chr18: 14,225,531-14,225,661 , GRCh37.p13 chr18: 14,225,530-14,225,660 ANKRD20A5P
    nsv5531889copy number variation1nstd206human GRCh38 chr18: 14,211,399-14,211,521 , GRCh37.p13 chr18: 14,211,398-14,211,520 ANKRD20A5P
    nsv5529944copy number variation1nstd206human GRCh38 chr18: 14,188,865-14,194,742 , GRCh37.p13 chr18: 14,188,864-14,194,741 ANKRD20A5P, RNU6-316P
    nsv5525509copy number variation1nstd206human GRCh38 chr18: 14,071,655-14,280,291 , GRCh37.p13 chr18: 14,071,654-14,280,290 NF1P5, ZNF519, 7 more genes
    nsv5419463mobile element insertion1nstd206human GRCh38 chr18: 14,221,317-14,221,368 , GRCh37.p13 chr18: 14,221,316-14,221,367 RHOT1P1, ANKRD20A5P
    nsv5324020copy number variation1nstd204human GRCh37.p13 chr18: 14,188,854-14,194,750 , GRCh38.p13 chr18: 14,188,855-14,194,751 RNU6-316P, ANKRD20A5P
    nsv5290347copy number variation1nstd204human GRCh38.p13 chr18: 14,188,901-14,194,700 , GRCh37.p13 chr18: 14,188,900-14,194,699 ANKRD20A5P, RNU6-316P
    nsv5288132copy number variation1nstd204human GRCh38.p13 chr18: 14,191,612-14,192,999 , GRCh37.p13 chr18: 14,191,611-14,192,998 ANKRD20A5P
    nsv5284905copy number variation1nstd204human GRCh38.p13 chr18: 14,188,846-14,194,675 , GRCh37.p13 chr18: 14,188,845-14,194,674 ANKRD20A5P, RNU6-316P
    nsv5158342mobile element insertion1nstd203human GRCh38 chr18: 14,221,307-14,221,317 , GRCh37.p13 chr18: 14,221,306-14,221,316 ANKRD20A5P, RHOT1P1
    nsv5158122mobile element insertion1nstd203human GRCh38 chr18: 14,221,305-14,221,317 , GRCh37.p13 chr18: 14,221,304-14,221,316 RHOT1P1, ANKRD20A5P
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