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 84

    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
    nsv6906752copy number variation1nstd229human GRCh38 chr11: 4,901,337-4,966,416 , GRCh37.p13 chr11: 4,922,567-4,987,646 OR51G2, OR51A7, 4 more genes
    nsv6903195copy number variation1nstd229human GRCh38 chr11: 4,899,601-4,966,400 , GRCh37.p13 chr11: 4,920,831-4,987,630 OR51A3P, OR51A2, 4 more genes
    nsv6903025copy number variation1nstd229human GRCh38 chr11: 4,682,156-5,202,827 , GRCh37.p13 chr11: 4,703,386-5,224,057 OR51V1, OR51L1, 39 more genes
    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
    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
    nsv6439692copy number variation1nstd223human GRCh38 chr11: 4,682,156-5,202,827 , GRCh37.p13 chr11: 4,703,386-5,224,057 OR51S1, OR51F1, 39 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
    nsv6291043copy number variation1nstd102humanLikely benign GRCh37 chr11: 4,937,852-5,037,488 , GRCh38.p12 chr11: 4,916,622-5,016,258 MMP26, OR51P1P, 6 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
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4607020copy number variation1nstd183human GRCh37 chr11: 4,928,585-4,968,117 , GRCh38.p12 chr11: 4,907,355-4,946,887 OR51G2, OR51A4, 3 more genes
    nsv4382560copy number variation1nstd173human GRCh37 chr11: 4,687,080-4,967,238 , GRCh38.p12 chr11: 4,665,850-4,946,008 OR51N1P, OR51A8P, 22 more genes
    nsv4381756copy number variation1nstd173human GRCh37 chr11: 4,167,416-5,153,276 , GRCh38.p12 chr11: 4,146,186-5,132,046 C11orf40, OR51H1, 62 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