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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099257copy number variation1nstd231human GRCh38.p12 chr1: 203,396,218-207,103,915 , GRCh37 chr1: 203,365,346-207,277,260 ATP2B4, AVPR1B, 116 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7048306inversion1nstd229human GRCh38 chr1: 203,741,746-203,785,833 , GRCh37.p13 chr1: 203,710,874-203,754,961 ATP2B4, LAX1, 1 more genes
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6676371copy number variation1nstd229human GRCh38 chr1: 203,646,216-203,646,239 , GRCh37.p13 chr1: 203,615,344-203,615,367 ATP2B4
    nsv6672569copy number variation1nstd229human GRCh38 chr1: 203,664,704-203,669,395 , GRCh37.p13 chr1: 203,633,832-203,638,523 ATP2B4
    nsv6670865copy number variation1nstd229human GRCh38 chr1: 203,637,096-203,638,973 , GRCh37.p13 chr1: 203,606,224-203,608,101 ATP2B4
    nsv6669454copy number variation1nstd229human GRCh38 chr1: 203,406,944-203,632,767 , GRCh37.p13 chr1: 203,376,072-203,601,895 OPTC, ATP2B4, 3 more genes
    nsv6668837copy number variation1nstd229human GRCh38 chr1: 203,661,563-203,664,601 , GRCh37.p13 chr1: 203,630,691-203,633,729 ATP2B4
    nsv6668594copy number variation1nstd229human GRCh38 chr1: 203,666,415-203,669,987 , GRCh37.p13 chr1: 203,635,543-203,639,115 ATP2B4
    nsv6668190copy number variation1nstd229human GRCh38 chr1: 203,671,814-203,671,869 , GRCh37.p13 chr1: 203,640,942-203,640,997 ATP2B4
    nsv6667694copy number variation1nstd229human GRCh38 chr1: 203,623,224-203,626,442 , GRCh37.p13 chr1: 203,592,352-203,595,570 ATP2B4
    nsv6662496copy number variation1nstd229human GRCh38 chr1: 203,687,432-203,690,703 , GRCh37.p13 chr1: 203,656,560-203,659,831 ATP2B4
    nsv6659100copy number variation1nstd229human GRCh38 chr1: 203,645,501-203,661,200 , GRCh37.p13 chr1: 203,614,629-203,630,328 NSA2P1, ATP2B4
    nsv6658844copy number variation1nstd229human GRCh38 chr1: 203,655,901-203,664,300 , GRCh37.p13 chr1: 203,625,029-203,633,428 NSA2P1, ATP2B4
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 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
    nsv6549848inversion1nstd223human GRCh38 chr1: 203,651,776-203,652,446 , GRCh37.p13 chr1: 203,620,904-203,621,574 ATP2B4
    nsv6547097inversion1nstd223human GRCh38 chr1: 203,718,587-203,718,799 , GRCh37.p13 chr1: 203,687,715-203,687,927 ATP2B4
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