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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094025copy number variation1nstd102humanPathogenic GRCh37 chr12: 110,646,956-110,765,842 , GRCh38.p12 chr12: 110,209,151-110,328,037 IFT81, ATP2A2
    nsv7093954copy number variation1nstd102humanPathogenic GRCh37 chr12: 110,581,167-110,581,370 , GRCh38.p12 chr12: 110,143,362-110,143,565 IFT81
    nsv6937461copy number variation1nstd229human GRCh38 chr12: 110,147,968-110,148,065 , GRCh37.p13 chr12: 110,585,773-110,585,870 IFT81
    nsv6934965copy number variation1nstd229human GRCh38 chr12: 110,199,101-110,202,300 , GRCh37.p13 chr12: 110,636,906-110,640,105 IFT81
    nsv6934331copy number variation1nstd229human GRCh38 chr12: 110,154,348-110,155,061 , GRCh37.p13 chr12: 110,592,153-110,592,866 IFT81
    nsv6932562copy number variation1nstd229human GRCh38 chr12: 110,125,736-110,130,862 , GRCh37.p13 chr12: 110,563,541-110,568,667 IFT81
    nsv6931732copy number variation1nstd229human GRCh38 chr12: 108,914,683-113,697,537 , GRCh37.p13 chr12: 109,308,459-114,135,342 PTPN11, RPL31P49, 111 more genes
    nsv6929412copy number variation1nstd229human GRCh38 chr12: 110,133,739-110,133,892 , GRCh37.p13 chr12: 110,571,544-110,571,697 IFT81
    nsv6922077copy number variation1nstd229human GRCh38 chr12: 110,201,117-110,214,115 , GRCh37.p13 chr12: 110,638,922-110,651,920 IFT81
    nsv6919948copy number variation1nstd229human GRCh38 chr12: 110,144,192-110,144,901 , GRCh37.p13 chr12: 110,581,997-110,582,706 IFT81
    nsv6919282copy number variation1nstd229human GRCh38 chr12: 110,160,084-110,160,140 , GRCh37.p13 chr12: 110,597,889-110,597,945 IFT81
    nsv6621491copy number variation1nstd224human GRCh37 chr12: 110,565,193-110,581,322 , GRCh38.p12 chr12: 110,127,388-110,143,517 IFT81
    nsv6621490copy number variation1nstd224human GRCh37 chr12: 110,557,312-110,630,498 , GRCh38.p12 chr12: 110,119,507-110,192,693 IFT81
    nsv6621400copy number variation1nstd224human GRCh37 chr12: 110,496,788-110,581,322 , GRCh38.p12 chr12: 110,058,983-110,143,517 LOC105369976, C12orf76, 1 more genes
    nsv6594234inversion1nstd223human GRCh38 chr12: 110,132,363-110,133,096 , GRCh37.p13 chr12: 110,570,168-110,570,901 IFT81
    nsv6593066inversion1nstd223human GRCh38 chr12: 110,187,268-110,188,360 , GRCh37.p13 chr12: 110,625,073-110,626,165 IFT81
    nsv6592284inversion1nstd223human GRCh38 chr12: 110,156,660-110,157,069 , GRCh37.p13 chr12: 110,594,465-110,594,874 IFT81
    nsv6591625inversion1nstd223human GRCh38 chr12: 110,131,097-110,131,605 , GRCh37.p13 chr12: 110,568,902-110,569,410 IFT81
    nsv6587727inversion1nstd223human GRCh38 chr12: 110,211,869-110,212,240 , GRCh37.p13 chr12: 110,649,674-110,650,045 IFT81
    nsv6587711inversion1nstd223human GRCh38 chr12: 110,191,368-110,191,942 , GRCh37.p13 chr12: 110,629,173-110,629,747 IFT81
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