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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3898872copy number variation1nstd102humanBenign GRCh37 chr11: 4,781,252-4,793,649 , GRCh38.p12 chr11: 4,760,022-4,772,419 OR51F1
    nsv4611763copy number variation1nstd183human GRCh37 chr11: 4,790,280-4,790,887 , GRCh38.p12 chr11: 4,769,050-4,769,657 OR51F1
    nsv1354579copy number variation1nstd122human NCBI36 chr11: 4,746,844-4,747,140 , GRCh37.p13 chr11: 4,790,268-4,790,564 , GRCh38.p12 chr11: 4,769,038-4,769,334 OR51F1
    esv3145551copy number variation1estd209human GRCh37 chr11: 4,790,873-4,790,874 , GRCh38.p12 chr11: 4,769,643-4,769,644 OR51F1
    nsv553175copy number variation2nstd54human NCBI36 chr11: 4,746,844-4,747,140 , GRCh37.p13 chr11: 4,790,268-4,790,564 , GRCh38.p12 chr11: 4,769,038-4,769,334 OR51F1
    esv3335338copy number variation1estd59human NCBI36 chr11: 4,743,252-4,746,550 , GRCh37.p13 chr11: 4,786,676-4,789,974 , GRCh38.p12 chr11: 4,765,446-4,768,744 OR51F1
    esv29053sequence alteration1estd20human NCBI36 chr11: 4,746,856-4,747,465 , GRCh37.p13 chr11: 4,790,280-4,790,889 , GRCh38.p12 chr11: 4,769,050-4,769,659 OR51F1
    esv20016copy number variation7estd20human NCBI36 chr11: 4,746,856-4,747,465 , GRCh37.p13 chr11: 4,790,280-4,790,889 , GRCh38.p12 chr11: 4,769,050-4,769,659 OR51F1
    esv2133598copy number variation1estd194human NCBI36 chr11: 4,747,450-4,747,451 , GRCh37.p13 chr11: 4,790,874-4,790,875 , GRCh38.p12 chr11: 4,769,644-4,769,645 OR51F1
    nsv39666copy number variation1nstd6human NCBI35 chr11: 4,745,883-4,745,891 , GRCh37.p13 chr11: 4,789,307-4,789,315 , GRCh38.p12 chr11: 4,768,077-4,768,085 OR51F1
    esv2885626insertion1estd209human GRCh37 chr11: 4,788,933-4,788,933 , GRCh38.p12 chr11: 4,767,703-4,767,703 OR51F1
    esv2403599insertion1estd194human NCBI36 chr11: 4,745,510-4,745,510 , GRCh37.p13 chr11: 4,788,934-4,788,934 , GRCh38.p12 chr11: 4,767,704-4,767,704 OR51F1
    esv1479945insertion1estd22human NCBI36 chr11: 4,745,512-4,745,512 , GRCh37.p13 chr11: 4,788,936-4,788,936 , GRCh38.p12 chr11: 4,767,706-4,767,706 OR51F1
    nsv34985insertion1nstd6human NCBI35 chr11: 4,745,513-4,745,513 , GRCh37.p13 chr11: 4,788,937-4,788,937 , GRCh38.p12 chr11: 4,767,707-4,767,707 OR51F1
    esv1809118copy number variation1estd188human NCBI36 chr11: 4,738,783-4,800,002 , GRCh37.p13 chr11: 4,782,207-4,843,426 , GRCh38.p12 chr11: 4,760,977-4,822,196 OR51F2, OR51N1P, 3 more genes
    esv1806557copy number variation1estd188human NCBI36 chr11: 4,735,009-4,777,057 , GRCh37.p13 chr11: 4,778,433-4,820,481 , GRCh38.p12 chr11: 4,757,203-4,799,251 OR51N1P, OR52Y1P, 1 more genes
    nsv1038862copy number variation1nstd100human NCBI36 chr11: 4,714,755-4,763,940 , GRCh37.p13 chr11: 4,758,179-4,807,364 , GRCh38.p12 chr11: 4,736,949-4,786,134 OR51F1, OR51F3P, 2 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
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