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Items: 1 to 20 of 531

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075918inversion1nstd229human GRCh38 chr9: 110,953,822-110,960,155 , GRCh37.p13 chr9: 113,716,102-113,722,435 LPAR1
    nsv7065142inversion1nstd229human GRCh38 chr9: 110,970,486-110,970,553 , GRCh37.p13 chr9: 113,732,766-113,732,833 LPAR1
    nsv6877424copy number variation1nstd229human GRCh38 chr9: 110,986,716-110,986,945 , GRCh37.p13 chr9: 113,748,996-113,749,225 LPAR1
    nsv6875512copy number variation1nstd229human GRCh38 chr9: 111,020,401-111,026,000 , GRCh37.p13 chr9: 113,782,681-113,788,280 LPAR1
    nsv6874581copy number variation1nstd229human GRCh38 chr9: 110,921,298-110,932,733 , GRCh37.p13 chr9: 113,683,578-113,695,013 LPAR1
    nsv6873711copy number variation1nstd229human GRCh38 chr9: 110,894,601-110,902,700 , GRCh37.p13 chr9: 113,656,881-113,664,980 RNU6-432P, LPAR1
    nsv6872448copy number variation1nstd229human GRCh38 chr9: 111,008,471-111,016,512 , GRCh37.p13 chr9: 113,770,751-113,778,792 LPAR1
    nsv6871645copy number variation1nstd229human GRCh38 chr9: 111,000,801-111,002,700 , GRCh37.p13 chr9: 113,763,081-113,764,980 LPAR1
    nsv6871587copy number variation1nstd229human GRCh38 chr9: 110,929,667-110,934,421 , GRCh37.p13 chr9: 113,691,947-113,696,701 LPAR1
    nsv6869885copy number variation1nstd229human GRCh38 chr9: 110,893,214-110,900,951 , GRCh37.p13 chr9: 113,655,494-113,663,231 LPAR1
    nsv6869629copy number variation1nstd229human GRCh38 chr9: 110,853,167-110,873,015 , GRCh37.p13 chr9: 113,615,447-113,635,295 LPAR1
    nsv6869379copy number variation1nstd229human GRCh38 chr9: 110,906,849-110,906,981 , GRCh37.p13 chr9: 113,669,129-113,669,261 LPAR1
    nsv6868777copy number variation1nstd229human GRCh38 chr9: 110,914,686-110,918,852 , GRCh37.p13 chr9: 113,676,966-113,681,132 LPAR1
    nsv6868447copy number variation1nstd229human GRCh38 chr9: 110,906,493-110,912,876 , GRCh37.p13 chr9: 113,668,773-113,675,156 LPAR1
    nsv6868215copy number variation1nstd229human GRCh38 chr9: 110,915,243-110,916,002 , GRCh37.p13 chr9: 113,677,523-113,678,282 LPAR1
    nsv6866952copy number variation1nstd229human GRCh38 chr9: 110,948,916-110,959,910 , GRCh37.p13 chr9: 113,711,196-113,722,190 LPAR1
    nsv6866190copy number variation1nstd229human GRCh38 chr9: 110,947,327-110,953,100 , GRCh37.p13 chr9: 113,709,607-113,715,380 LPAR1
    nsv6866125copy number variation1nstd229human GRCh38 chr9: 111,002,801-111,008,800 , GRCh37.p13 chr9: 113,765,081-113,771,080 LPAR1
    nsv6864914copy number variation1nstd229human GRCh38 chr9: 110,964,378-110,984,100 , GRCh37.p13 chr9: 113,726,658-113,746,380 LPAR1
    nsv6864686copy number variation1nstd229human GRCh38 chr9: 110,998,048-111,009,829 , GRCh37.p13 chr9: 113,760,328-113,772,109 LPAR1
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