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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099264copy number variation1nstd231human GRCh38.p12 chr1: 222,151,895-226,849,338 , GRCh37 chr1: 222,325,237-227,037,039 PARP1, CAPN2, 99 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7054253inversion1nstd229human GRCh38 chr1: 225,921,423-226,427,421 , GRCh37.p13 chr1: 226,109,123-226,615,122 H3-3A, ACBD3, 15 more genes
    nsv7053157inversion1nstd229human GRCh38 chr1: 225,921,281-226,429,584 , GRCh37.p13 chr1: 226,108,981-226,617,285 RPL34P7, YBX1P9, 15 more genes
    nsv6676832copy number variation1nstd229human GRCh38 chr1: 226,301,824-226,305,998 , GRCh37.p13 chr1: 226,489,525-226,493,699 LIN9
    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
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 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
    nsv6554507inversion1nstd223human GRCh38 chr1: 226,256,859-226,257,902 , GRCh37.p13 chr1: 226,444,560-226,445,603 LIN9
    nsv6553316inversion1nstd223human GRCh38 chr1: 226,294,544-226,294,907 , GRCh37.p13 chr1: 226,482,245-226,482,608 LIN9
    nsv6550326inversion1nstd223human GRCh38 chr1: 226,236,462-226,237,546 , GRCh37.p13 chr1: 226,424,163-226,425,247 LIN9
    nsv6550158inversion1nstd223human GRCh38 chr1: 226,253,039-226,254,063 , GRCh37.p13 chr1: 226,440,740-226,441,764 LIN9
    nsv6543411inversion1nstd223human GRCh38 chr1: 226,298,189-226,298,685 , GRCh37.p13 chr1: 226,485,890-226,486,386 LIN9
    nsv6542389inversion1nstd223human GRCh38 chr1: 226,258,608-226,259,102 , GRCh37.p13 chr1: 226,446,309-226,446,803 LIN9
    nsv6541376inversion1nstd223human GRCh38 chr1: 226,288,169-226,289,101 , GRCh37.p13 chr1: 226,475,870-226,476,802 LIN9
    nsv6537290inversion1nstd223human GRCh38 chr1: 226,264,156-226,265,792 , GRCh37.p13 chr1: 226,451,857-226,453,493 LIN9
    nsv6334192copy number variation1nstd223human GRCh38 chr1: 226,253,156-226,254,804 , GRCh37.p13 chr1: 226,440,857-226,442,505 LIN9
    nsv6332133copy number variation1nstd223human GRCh38 chr1: 226,282,088-226,282,504 , GRCh37.p13 chr1: 226,469,789-226,470,205 LIN9
    nsv6331204copy number variation1nstd223human GRCh38 chr1: 226,234,020-226,236,226 , GRCh37.p13 chr1: 226,421,721-226,423,927 LIN9
    nsv6324615copy number variation1nstd223human GRCh38 chr1: 221,964,560-227,275,239 , GRCh37.p13 chr1: 222,137,902-227,462,940 LEFTY2, HHIPL2, 109 more genes
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