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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145041copy number variation1nstd232human GRCh37.p13 chr9: 114,135,516-114,135,593 , GRCh38.p12 chr9: 111,373,236-111,373,313 ECPAS
    nsv7142044insertion1nstd232human GRCh37.p13 chr9: 114,169,708-114,169,708 , GRCh38.p12 chr9: 111,407,428-111,407,428 ECPAS
    nsv7060958inversion1nstd229human GRCh38 chr9: 111,470,546-111,481,226 , GRCh37.p13 chr9: 114,232,826-114,243,506 ECPAS
    nsv7059237inversion1nstd229human GRCh38 chr9: 111,465,999-111,481,335 , GRCh37.p13 chr9: 114,228,279-114,243,615 ECPAS
    nsv6876027copy number variation1nstd229human GRCh38 chr9: 111,363,211-111,367,652 , GRCh37.p13 chr9: 114,125,491-114,129,932 ECPAS
    nsv6874962copy number variation1nstd229human GRCh38 chr9: 111,466,267-111,470,521 , GRCh37.p13 chr9: 114,228,547-114,232,801 ECPAS
    nsv6873884copy number variation1nstd229human GRCh38 chr9: 111,470,817-111,470,977 , GRCh37.p13 chr9: 114,233,097-114,233,257 ECPAS
    nsv6871994copy number variation1nstd229human GRCh38 chr9: 111,475,070-111,478,924 , GRCh37.p13 chr9: 114,237,350-114,241,204 ECPAS
    nsv6870747copy number variation1nstd229human GRCh38 chr9: 111,461,446-111,461,577 , GRCh37.p13 chr9: 114,223,726-114,223,857 ECPAS
    nsv6868308copy number variation1nstd229human GRCh38 chr9: 111,465,999-111,470,546 , GRCh37.p13 chr9: 114,228,279-114,232,826 ECPAS
    nsv6866244copy number variation1nstd229human GRCh38 chr9: 111,404,501-111,407,400 , GRCh37.p13 chr9: 114,166,781-114,169,680 ECPAS
    nsv6863962copy number variation1nstd229human GRCh38 chr9: 111,403,391-111,407,455 , GRCh37.p13 chr9: 114,165,671-114,169,735 ECPAS
    nsv6863854copy number variation1nstd229human GRCh38 chr9: 111,405,101-111,407,400 , GRCh37.p13 chr9: 114,167,381-114,169,680 ECPAS
    nsv6862872copy number variation1nstd229human GRCh38 chr9: 111,476,055-111,476,468 , GRCh37.p13 chr9: 114,238,335-114,238,748 ECPAS
    nsv6861205copy number variation1nstd229human GRCh38 chr9: 111,475,501-111,541,400 , GRCh37.p13 chr9: 114,237,781-114,303,680 ZNF483, ECPAS
    nsv6860045copy number variation1nstd229human GRCh38 chr9: 111,392,200-111,464,420 , GRCh37.p13 chr9: 114,154,480-114,226,700 ECPAS, RNA5SP294
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6571501inversion1nstd223human GRCh38 chr9: 111,469,823-111,470,601 , GRCh37.p13 chr9: 114,232,103-114,232,881 ECPAS
    nsv6571293inversion1nstd223human GRCh38 chr9: 111,396,885-111,398,638 , GRCh37.p13 chr9: 114,159,165-114,160,918 ECPAS
    nsv6569305inversion1nstd223human GRCh38 chr9: 111,469,640-111,470,317 , GRCh37.p13 chr9: 114,231,920-114,232,597 ECPAS
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