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Items: 1 to 20 of 938

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145051insertion1nstd232human GRCh37.p13 chr10: 18,503,078-18,503,078 , GRCh38.p12 chr10: 18,214,149-18,214,149 CACNB2
    nsv7144603copy number variation1nstd232human GRCh37.p13 chr10: 18,731,875-18,731,942 , GRCh38.p12 chr10: 18,442,946-18,443,013 CACNB2
    nsv7142138insertion1nstd232human GRCh37.p13 chr10: 18,503,077-18,503,077 , GRCh38.p12 chr10: 18,214,148-18,214,148 CACNB2
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093870copy number variation1nstd102humanUncertain significance GRCh37 chr10: 18,629,856-18,629,926 , GRCh38.p12 chr10: 18,340,927-18,340,997 CACNB2
    nsv7093787copy number variation1nstd102humanUncertain significance GRCh37 chr10: 18,807,245-18,828,653 , GRCh38.p12 chr10: 18,518,316-18,539,724 NSUN6, CACNB2
    nsv7074105inversion1nstd229human GRCh38 chr10: 17,945,641-22,801,235 , GRCh37.p13 chr10: 18,252,931-23,090,164 UBE2V2P1, LOC105376450, 62 more genes
    nsv7071962inversion1nstd229human GRCh38 chr10: 18,276,541-18,279,754 , GRCh37.p13 chr10: 18,565,470-18,568,683 CACNB2
    nsv7059506inversion1nstd229human GRCh38 chr10: 18,306,087-18,326,786 , GRCh37.p13 chr10: 18,595,016-18,615,715 CACNB2
    nsv7058980inversion1nstd229human GRCh38 chr10: 18,388,400-18,395,112 , GRCh37.p13 chr10: 18,677,329-18,684,041 CACNB2
    nsv6897987copy number variation1nstd229human GRCh38 chr10: 18,256,295-18,256,778 , GRCh37.p13 chr10: 18,545,224-18,545,707 CACNB2, LOC107984213
    nsv6897667copy number variation1nstd229human GRCh38 chr10: 18,445,801-18,505,000 , GRCh37.p13 chr10: 18,734,730-18,793,929 CACNB2
    nsv6897593copy number variation1nstd229human GRCh38 chr10: 18,380,501-18,399,300 , GRCh37.p13 chr10: 18,669,430-18,688,229 CACNB2
    nsv6897496copy number variation1nstd229human GRCh38 chr10: 18,515,535-18,515,948 , GRCh37.p13 chr10: 18,804,464-18,804,877 CACNB2, NSUN6
    nsv6897352copy number variation1nstd229human GRCh38 chr10: 18,222,142-18,226,848 , GRCh37.p13 chr10: 18,511,071-18,515,777 CACNB2
    nsv6896550copy number variation1nstd229human GRCh38 chr10: 18,415,006-18,419,871 , GRCh37.p13 chr10: 18,703,935-18,708,800 CACNB2
    nsv6896432copy number variation1nstd229human GRCh38 chr10: 18,526,957-18,527,067 , GRCh37.p13 chr10: 18,815,886-18,815,996 CACNB2, NSUN6
    nsv6895930copy number variation1nstd229human GRCh38 chr10: 18,213,499-18,217,285 , GRCh37.p13 chr10: 18,502,428-18,506,214 CACNB2
    nsv6895713copy number variation1nstd229human GRCh38 chr10: 18,225,190-18,232,169 , GRCh37.p13 chr10: 18,514,119-18,521,098 CACNB2
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