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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076259inversion1nstd229human GRCh38 chr18: 32,207,530-32,315,177 , GRCh37.p13 chr18: 29,787,493-29,895,140 GAREM1, MEP1B
    nsv7074645inversion1nstd229human GRCh38 chr18: 30,537,670-35,063,371 , GRCh37.p13 chr18: 28,117,636-32,643,335 DSC1, RN7SKP44, 46 more genes
    nsv7071971inversion1nstd229human GRCh38 chr18: 31,938,930-32,318,381 , GRCh37.p13 chr18: 29,518,893-29,898,344 TRAPPC8, RNA5SP453, 9 more genes
    nsv7060883inversion1nstd229human GRCh38 chr18: 32,210,899-32,213,320 , GRCh37.p13 chr18: 29,790,862-29,793,283 MEP1B
    nsv7009273copy number variation1nstd229human GRCh38 chr18: 32,206,933-32,263,387 , GRCh37.p13 chr18: 29,786,896-29,843,350 GAREM1, MEP1B
    nsv7008011copy number variation1nstd229human GRCh38 chr18: 32,210,092-32,214,471 , GRCh37.p13 chr18: 29,790,055-29,794,434 MEP1B
    nsv7004163copy number variation1nstd229human GRCh38 chr18: 32,214,428-32,214,809 , GRCh37.p13 chr18: 29,794,391-29,794,772 MEP1B
    nsv7004076copy number variation1nstd229human GRCh38 chr18: 31,888,813-32,220,544 , GRCh37.p13 chr18: 29,468,776-29,800,507 TRAPPC8, RNU6-1050P, 9 more genes
    nsv7003751copy number variation1nstd229human GRCh38 chr18: 32,126,701-32,318,400 , GRCh37.p13 chr18: 29,706,664-29,898,363 GAREM1, RNF138, 3 more genes
    nsv7000118copy number variation1nstd229human GRCh38 chr18: 32,222,265-32,222,298 , GRCh37.p13 chr18: 29,802,228-29,802,261 MEP1B
    nsv6999513copy number variation1nstd229human GRCh38 chr18: 32,204,072-32,204,280 , GRCh37.p13 chr18: 29,784,035-29,784,243 MEP1B
    nsv6624149copy number variation1nstd224human GRCh37 chr18: 29,731,080-29,806,853 , GRCh38.p12 chr18: 32,151,117-32,226,890 MEP1B, CLUHP6, 1 more genes
    nsv6586488inversion1nstd223human GRCh38 chr18: 31,938,930-32,318,379 , GRCh37.p13 chr18: 29,518,893-29,898,342 MEP1B, RNF138, 9 more genes
    nsv6586126inversion1nstd223human GRCh38 chr18: 31,785,259-32,556,165 , GRCh37.p13 chr18: 29,365,222-30,136,128 WBP11P1, LOC100421591, 13 more genes
    nsv6534515copy number variation1nstd223human GRCh38 chr18: 32,151,901-32,231,000 , GRCh37.p13 chr18: 29,731,864-29,810,963 MEP1B, CLUHP6, 1 more genes
    nsv6533200copy number variation1nstd223human GRCh38 chr18: 32,205,173-32,206,179 , GRCh37.p13 chr18: 29,785,136-29,786,142 MEP1B
    nsv6518564copy number variation1nstd223human GRCh38 chr18: 32,120,858-32,508,311 , GRCh37.p13 chr18: 29,700,821-30,088,274 MEP1B, RNF138, 4 more genes
    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
    nsv6291549copy number variation1nstd102humanLikely benign GRCh37 chr18: 29,734,579-29,807,636 , GRCh38.p12 chr18: 32,154,616-32,227,673 MEP1B, CLUHP6, 1 more genes
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