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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073256inversion1nstd229human GRCh38 chr13: 19,714,497-24,851,015 , GRCh37.p13 chr13: 20,288,637-25,425,153 SPATA13, IFT88, 114 more genes
    nsv7072424inversion1nstd229human GRCh38 chr13: 20,061,787-21,405,901 , GRCh37.p13 chr13: 20,635,927-21,980,040 IPPKP1, CRYL1, 41 more genes
    nsv7071522inversion1nstd229human GRCh38 chr13: 20,968,762-20,972,302 , GRCh37.p13 chr13: 21,542,901-21,546,441 LATS2
    nsv7071404inversion1nstd229human GRCh38 chr13: 20,981,175-21,203,806 , GRCh37.p13 chr13: 21,555,314-21,777,945 LATS2, RNU4-9P, 6 more genes
    nsv7071368inversion1nstd229human GRCh38 chr13: 19,560,696-21,260,853 , GRCh37.p13 chr13: 20,134,836-21,834,992 ZMYM2, EEF1AKMT1, 44 more genes
    nsv7071034inversion1nstd229human GRCh38 chr13: 19,239,514-24,381,508 , GRCh37.p13 chr13: 19,813,654-24,955,646 BASP1P1, ZMYM5, 111 more genes
    nsv7068264inversion1nstd229human GRCh38 chr13: 20,443,147-22,597,794 , GRCh37.p13 chr13: 21,017,286-23,171,933 RPSAP54, IL17D, 43 more genes
    nsv7067925inversion1nstd229human GRCh38 chr13: 19,527,899-24,671,591 , GRCh37.p13 chr13: 20,102,039-25,245,729 TPTE2-AS1, TNFRSF19, 112 more genes
    nsv7065933inversion1nstd229human GRCh38 chr13: 19,560,717-21,260,795 , GRCh37.p13 chr13: 20,134,857-21,834,934 LOC105370101, GJB2, 44 more genes
    nsv7065531inversion1nstd229human GRCh38 chr13: 20,507,648-21,110,224 , GRCh37.p13 chr13: 21,081,787-21,684,363 HNRNPA1P30, XPO4, 17 more genes
    nsv7061961inversion1nstd229human GRCh38 chr13: 20,241,182-21,970,619 , GRCh37.p13 chr13: 20,815,321-22,544,758 RNA5SP25, CRYL1, 40 more genes
    nsv7061118inversion1nstd229human GRCh38 chr13: 20,936,120-21,524,007 , GRCh37.p13 chr13: 21,510,259-22,098,146 IPPKP1, LATS2, 22 more genes
    nsv7058292inversion1nstd229human GRCh38 chr13: 19,736,413-23,270,103 , GRCh37.p13 chr13: 20,310,553-23,844,242 PPIAP28, RPL7AP73, 75 more genes
    nsv6937136copy number variation1nstd229human GRCh38 chr13: 20,992,079-21,000,181 , GRCh37.p13 chr13: 21,566,218-21,574,320 LATS2
    nsv6936717copy number variation1nstd229human GRCh38 chr13: 21,017,909-21,027,836 , GRCh37.p13 chr13: 21,592,048-21,601,975 LATS2
    nsv6935780copy number variation1nstd229human GRCh38 chr13: 21,010,141-21,035,961 , GRCh37.p13 chr13: 21,584,280-21,610,100 LATS2
    nsv6934770copy number variation1nstd229human GRCh38 chr13: 21,005,901-21,020,100 , GRCh37.p13 chr13: 21,580,040-21,594,239 LATS2
    nsv6932713copy number variation1nstd229human GRCh38 chr13: 19,442,684-24,587,300 , GRCh37.p13 chr13: 20,016,824-25,161,438 CEND1P2, MTCO3P2, 112 more genes
    nsv6930225copy number variation1nstd229human GRCh38 chr13: 20,879,987-21,208,515 , GRCh37.p13 chr13: 21,454,126-21,782,654 SKA3, HNRNPA1P30, 12 more genes
    nsv6927974copy number variation1nstd229human GRCh38 chr13: 21,003,699-21,009,122 , GRCh37.p13 chr13: 21,577,838-21,583,261 LATS2
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