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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7038216inversion1nstd229human GRCh38 chr1: 221,729,601-221,729,680 , GRCh37.p13 chr1: 221,902,943-221,903,022 DUSP10
    nsv6677013copy number variation1nstd229human GRCh38 chr1: 221,730,101-221,732,300 , GRCh37.p13 chr1: 221,903,443-221,905,642 DUSP10
    nsv6676326copy number variation1nstd229human GRCh38 chr1: 221,707,478-221,711,201 , GRCh37.p13 chr1: 221,880,820-221,884,543 DUSP10
    nsv6669788copy number variation1nstd229human GRCh38 chr1: 221,711,840-221,712,223 , GRCh37.p13 chr1: 221,885,182-221,885,565 DUSP10
    nsv6669551copy number variation1nstd229human GRCh38 chr1: 221,588,301-221,771,255 , GRCh37.p13 chr1: 221,761,643-221,944,597 DUSP10
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636736copy number variation1nstd102humanUncertain significance GRCh37 chr1: 221,325,488-225,804,228 , GRCh38.p12 chr1: 221,152,146-225,616,526 BROX, LINC02765, 77 more genes
    nsv6636311copy number variation1nstd102humanUncertain significance GRCh37 chr1: 221,833,606-222,245,603 , GRCh38.p12 chr1: 221,660,264-222,072,261 LINC01655, LINC01705, 4 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6330140copy number variation1nstd223human GRCh38 chr1: 221,726,401-221,727,600 , GRCh37.p13 chr1: 221,899,743-221,900,942 DUSP10
    nsv6317933copy number variation1nstd223human GRCh38 chr1: 221,521,201-221,727,100 , GRCh37.p13 chr1: 221,694,543-221,900,442 LOC107985462, DUSP10, 2 more genes
    nsv6313779copy number variation1nstd102humanPathogenic GRCh37 chr1: 221,303,919-227,461,343 , GRCh38.p12 chr1: 221,130,577-227,273,642 ENAH, HHIPL2, 119 more genes
    nsv6290569copy number variation1nstd102humanPathogenic GRCh37 chr1: 215,199,578-223,035,427 , GRCh38.p12 chr1: 215,026,235-222,862,085 SPATA17, BROX, 97 more genes
    nsv6133979copy number variation1nstd213human GRCh37 chr1: 221,280,000-222,220,001 , GRCh38.p12 chr1: 221,106,658-222,046,659 DUSP10, LOC100132626, 12 more genes
    nsv6133857copy number variation1nstd213human GRCh37 chr1: 215,920,000-223,130,001 , GRCh38.p12 chr1: 215,746,658-222,956,659 BPNT1, HHIPL2, 95 more genes
    nsv6133630copy number variation2nstd213human GRCh37 chr1: 206,490,000-223,720,001 , GRCh38.p12 chr1: 206,316,655-223,546,636 ATP5MC2P1, CENPF, 269 more genes
    nsv5687595mobile element insertion1nstd211human GRCh38 chr1: 221,707,818-221,707,818 , GRCh37.p13 chr1: 221,881,160-221,881,160 , DUSP10
    nsv5538095insertion1nstd206human GRCh38 chr1: 221,707,818-221,707,850 , GRCh37.p13 chr1: 221,881,160-221,881,192 , DUSP10
    nsv5537879insertion1nstd206human GRCh38 chr1: 221,700,580-221,700,620 , GRCh37.p13 chr1: 221,873,922-221,873,962 DUSP10
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