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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7094636copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,857,986-81,282,132 , GRCh38.p12 chr15: 78,565,644-80,989,791 LOC646934, RNU6-415P, 51 more genes
    nsv7076478inversion1nstd229human GRCh38 chr15: 79,261,836-81,280,491 , GRCh37.p13 chr15: 79,554,178-81,572,832 CFAP161, TMED3, 34 more genes
    nsv7063463inversion1nstd229human GRCh38 chr15: 75,234,241-81,337,543 , GRCh37.p13 chr15: 75,526,582-81,629,884 RN7SL327P, LOC105370910, 138 more genes
    nsv7063009inversion1nstd229human GRCh38 chr15: 80,220,949-81,163,179 , GRCh37.p13 chr15: 80,513,291-81,455,520 CEMIP, ARNT2, 13 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv6977776copy number variation1nstd229human GRCh38 chr15: 80,199,067-80,199,636 , GRCh37.p13 chr15: 80,491,409-80,491,978 CTXND1
    nsv6977404copy number variation1nstd229human GRCh38 chr15: 80,228,351-80,230,032 , GRCh37.p13 chr15: 80,520,693-80,522,374 CTXND1
    nsv6977074copy number variation1nstd229human GRCh38 chr15: 80,220,168-80,225,966 , GRCh37.p13 chr15: 80,512,510-80,518,308 CTXND1
    nsv6977011copy number variation1nstd229human GRCh38 chr15: 80,238,358-80,250,844 , GRCh37.p13 chr15: 80,530,700-80,543,186 CTXND1
    nsv6970273copy number variation1nstd229human GRCh38 chr15: 80,248,251-80,258,612 , GRCh37.p13 chr15: 80,540,593-80,550,954 CTXND1
    nsv6969044copy number variation1nstd229human GRCh38 chr15: 77,623,918-81,694,021 , GRCh37.p13 chr15: 77,916,260-81,986,362 ST20-MTHFS, CSPG4P13, 87 more genes
    nsv6967598copy number variation1nstd229human GRCh38 chr15: 80,228,720-80,234,510 , GRCh37.p13 chr15: 80,521,062-80,526,852 CTXND1
    nsv6961734copy number variation1nstd229human GRCh38 chr15: 80,237,434-80,256,444 , GRCh37.p13 chr15: 80,529,776-80,548,786 CTXND1
    nsv6960112copy number variation1nstd229human GRCh38 chr15: 80,220,501-80,239,100 , GRCh37.p13 chr15: 80,512,843-80,531,442 CTXND1
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6637608copy number variation1nstd102humanUncertain significance GRCh37 chr15: 79,996,626-82,097,796 , GRCh38.p12 chr15: 79,704,284-81,805,455 ARNT2, LOC105370921, 31 more genes
    nsv6592438inversion1nstd223human GRCh38 chr15: 80,238,025-80,238,514 , GRCh37.p13 chr15: 80,530,367-80,530,856 CTXND1
    nsv6590502inversion1nstd223human GRCh38 chr15: 80,238,009-80,238,525 , GRCh37.p13 chr15: 80,530,351-80,530,867 CTXND1
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