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 123

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137096copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,094,756-5,785,959 , GRCh38.p12 chr11: 5,073,526-5,764,729 OR51J1, OLFM5P, 52 more genes
    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
    nsv6916174copy number variation1nstd229human GRCh38 chr11: 5,447,942-5,467,900 , GRCh37.p13 chr11: 5,469,172-5,489,130 OR51B5, OR51A10P, 1 more genes
    nsv6910790copy number variation1nstd229human GRCh38 chr11: 5,368,252-5,542,054 , GRCh37.p13 chr11: 5,389,482-5,563,284 OR51K1P, OR51B5, 11 more genes
    nsv6904962copy number variation1nstd229human GRCh38 chr11: 5,412,518-5,475,696 , GRCh37.p13 chr11: 5,433,748-5,496,926 OR51A10P, OR51B5, 4 more genes
    nsv6900302copy number variation1nstd229human GRCh38 chr11: 5,409,708-5,471,203 , GRCh37.p13 chr11: 5,430,938-5,492,433 OR51A10P, OR51K1P, 4 more genes
    nsv6898769copy number variation1nstd229human GRCh38 chr11: 5,442,003-5,689,638 , GRCh37.p13 chr11: 5,463,233-5,710,868 TRIM6, TRIM22, 19 more genes
    nsv6638042copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,361,272-5,660,023 , GRCh38.p12 chr11: 5,340,042-5,638,793 OR51A10P, OR52H2P, 24 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
    nsv6637653copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,439,244-5,570,043 , GRCh38.p12 chr11: 5,418,014-5,548,813 OLFM5P, UBQLN3, 10 more genes
    nsv6637234copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,279,153-5,619,949 , GRCh38.p12 chr11: 5,257,923-5,598,719 OR51A10P, OR51B5, 29 more genes
    nsv6621247copy number variation2nstd224human GRCh37 chr11: 5,431,986-5,491,183 , GRCh38.p12 chr11: 5,410,756-5,469,953 OR51K1P, OR51A10P, 4 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
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6290806copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,373,646-5,519,671 , GRCh38.p12 chr11: 5,352,416-5,498,441 OR51Q1, OR51B6, 10 more genes
    nsv6290738copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,488,908-5,701,819 , GRCh38.p12 chr11: 5,467,678-5,680,589 UBQLN3, OLFM5P, 16 more genes
    nsv6033294copy number variation1nstd212human GRCh37.p13 chr11: 5,430,938-5,492,430 , GRCh38 chr11: 5,409,708-5,471,200 OR51K1P, OR51A10P, 4 more genes
    nsv5506878copy number variation1nstd206human GRCh38 chr11: 5,464,000-5,676,000 , GRCh37.p13 chr11: 5,485,230-5,697,230 OR52V1P, HNRNPA1P53, 16 more genes
    nsv5495573copy number variation1nstd206human GRCh38 chr11: 5,409,708-5,471,199 , GRCh37.p13 chr11: 5,430,938-5,492,429 OR51K1P, OR51A10P, 4 more genes
    nsv4833520copy number variation1nstd200human GRCh37 chr11: 5,433,133-5,568,488 , GRCh38.p12 chr11: 5,411,903-5,547,258 OR51Q1, UBQLNL, 10 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