U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 153

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6916237copy number variation1nstd229human GRCh38 chr11: 4,369,424-4,697,710 , GRCh37.p13 chr11: 4,390,654-4,718,940 TRIM68, OR51E2, 17 more genes
    nsv6916129copy number variation1nstd229human GRCh38 chr11: 3,833,721-4,728,036 , GRCh37.p13 chr11: 3,854,951-4,749,266 OR52K1, OR52B4, 39 more genes
    nsv6914951copy number variation1nstd229human GRCh38 chr11: 4,515,180-4,719,642 , GRCh37.p13 chr11: 4,536,410-4,740,872 OR51A9P, OR52M1, 12 more genes
    nsv6907396copy number variation1nstd229human GRCh38 chr11: 4,560,919-4,669,992 , GRCh37.p13 chr11: 4,582,149-4,691,222 TRIM68, OR52I2, 6 more genes
    nsv6906935copy number variation1nstd229human GRCh38 chr11: 4,646,501-4,650,500 , GRCh37.p13 chr11: 4,667,731-4,671,730 OR51E1
    nsv6904677copy number variation1nstd229human GRCh38 chr11: 4,638,701-4,650,500 , GRCh37.p13 chr11: 4,659,931-4,671,730 OR51E1, OR51D1
    nsv6902995copy number variation1nstd229human GRCh38 chr11: 4,619,101-5,268,938 , GRCh37.p13 chr11: 4,640,331-5,290,168 OR51A9P, OR51F1, 50 more genes
    nsv6638006copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,384,773-4,681,230 , GRCh38.p12 chr11: 4,363,543-4,660,000 OR51R1P, OR52I1, 15 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 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
    nsv6450577copy number variation1nstd223human GRCh38 chr11: 4,619,075-5,268,953 , GRCh37.p13 chr11: 4,640,305-5,290,183 OR52J1P, OR51F2, 50 more genes
    nsv6448771copy number variation1nstd223human GRCh38 chr11: 4,638,733-4,650,443 , GRCh37.p13 chr11: 4,659,963-4,671,673 OR51E1, OR51D1
    nsv6447516copy number variation1nstd223human GRCh38 chr11: 4,651,262-4,651,632 , GRCh37.p13 chr11: 4,672,492-4,672,862 OR51E1
    nsv6442818copy number variation1nstd223human GRCh38 chr11: 4,560,601-4,670,000 , GRCh37.p13 chr11: 4,581,831-4,691,230 TRIM68, C11orf40, 6 more genes
    nsv6438415copy number variation1nstd223human GRCh38 chr11: 4,449,872-4,656,651 , GRCh37.p13 chr11: 4,471,102-4,677,881 OR52I1, OR52K2, 9 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6302159copy number variation1nstd186human GRCh37 chr11: 4,673,171-4,673,244 , GRCh38.p12 chr11: 4,651,941-4,652,014 OR51E1
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6132106copy number variation1nstd213human GRCh37 chr11: 4,510,000-5,300,001 , GRCh38.p12 chr11: 4,488,770-5,278,771 HBB, HBBP1, 57 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center