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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068298inversion1nstd229human GRCh38 chr9: 84,320,139-84,356,701 , GRCh37.p13 chr9: 86,935,054-86,971,616 SLC28A3
    nsv7067775inversion1nstd229human GRCh38 chr9: 83,864,984-85,758,960 , GRCh37.p13 chr9: 86,479,899-88,373,875 LOC105376335, LOC101927575, 20 more genes
    nsv7066971inversion1nstd229human GRCh38 chr9: 84,305,508-84,307,522 , GRCh37.p13 chr9: 86,920,423-86,922,437 SLC28A3
    nsv7059796inversion1nstd229human GRCh38 chr9: 83,885,955-85,843,950 , GRCh37.p13 chr9: 86,500,870-88,458,865 HNRNPK, LOC105376121, 21 more genes
    nsv6875681copy number variation1nstd229human GRCh38 chr9: 84,350,065-84,356,573 , GRCh37.p13 chr9: 86,964,980-86,971,488 SLC28A3
    nsv6875495copy number variation1nstd229human GRCh38 chr9: 84,148,327-84,497,497 , GRCh37.p13 chr9: 86,763,242-87,112,412 LOC102724036, SLC28A3, 1 more genes
    nsv6874852copy number variation1nstd229human GRCh38 chr9: 84,143,848-84,815,976 , GRCh37.p13 chr9: 86,758,763-87,430,891 LOC102724036, SLC28A3, 2 more genes
    nsv6869798copy number variation1nstd229human GRCh38 chr9: 84,256,210-84,274,134 , GRCh37.p13 chr9: 86,871,125-86,889,049 SLC28A3
    nsv6862640copy number variation1nstd229human GRCh38 chr9: 84,355,871-84,356,245 , GRCh37.p13 chr9: 86,970,786-86,971,160 SLC28A3
    nsv6862254copy number variation1nstd229human GRCh38 chr9: 83,872,064-85,094,694 , GRCh37.p13 chr9: 86,486,979-87,709,609 LOC101927575, NTRK2, 12 more genes
    nsv6862055copy number variation1nstd229human GRCh38 chr9: 84,276,817-84,277,709 , GRCh37.p13 chr9: 86,891,732-86,892,624 SLC28A3-AS1, SLC28A3
    nsv6861598copy number variation1nstd229human GRCh38 chr9: 84,203,132-84,484,309 , GRCh37.p13 chr9: 86,818,047-87,099,224 SLC28A3, SLC28A3-AS1, 1 more genes
    nsv6859701copy number variation1nstd229human GRCh38 chr9: 84,318,043-84,318,099 , GRCh37.p13 chr9: 86,932,958-86,933,014 SLC28A3
    nsv6859032copy number variation1nstd229human GRCh38 chr9: 84,345,901-84,583,400 , GRCh37.p13 chr9: 86,960,816-87,198,315 LOC102724036, SLC28A3
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6575135inversion1nstd223human GRCh38 chr9: 84,341,288-84,341,999 , GRCh37.p13 chr9: 86,956,203-86,956,914 SLC28A3
    nsv6568256inversion1nstd223human GRCh38 chr9: 84,352,394-84,352,826 , GRCh37.p13 chr9: 86,967,309-86,967,741 SLC28A3
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 more genes
    nsv6565743inversion1nstd223human GRCh38 chr9: 84,311,753-84,312,186 , GRCh37.p13 chr9: 86,926,668-86,927,101 SLC28A3
    nsv6561466inversion1nstd223human GRCh38 chr9: 84,359,019-84,359,888 , GRCh37.p13 chr9: 86,973,934-86,974,803 SLC28A3
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