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 171

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv6917112copy number variation1nstd229human GRCh38 chr11: 3,812,770-3,816,722 , GRCh37.p13 chr11: 3,834,000-3,837,952 PGAP2
    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
    nsv6913358copy number variation1nstd229human GRCh38 chr11: 3,812,101-3,814,700 , GRCh37.p13 chr11: 3,833,331-3,835,930 PGAP2
    nsv6905004copy number variation1nstd229human GRCh38 chr11: 3,819,668-3,821,899 , GRCh37.p13 chr11: 3,840,898-3,843,129 PGAP2
    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
    nsv6455056copy number variation1nstd223human GRCh38 chr11: 3,812,770-3,816,713 , GRCh37.p13 chr11: 3,834,000-3,837,943 PGAP2
    nsv6453649copy number variation1nstd223human GRCh38 chr11: 3,800,581-3,821,529 , GRCh37.p13 chr11: 3,821,811-3,842,759 PGAP2
    nsv6438165copy number variation1nstd223human GRCh38 chr11: 737,066-3,896,161 , GRCh37.p13 chr11: 737,066-3,917,391 RNU6-878P, CARS1-AS1, 123 more genes
    nsv6436998copy number variation1nstd223human GRCh38 chr11: 3,785,042-3,800,716 , GRCh37.p13 chr11: 3,806,272-3,821,946 NUP98, PGAP2
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6309212copy number variation1nstd102humanUncertain significance GRCh37 chr11: 3,832,490-4,113,028 , GRCh38.p12 chr11: 3,811,260-4,091,798 STIM1-AS1, RHOG, 7 more genes
    nsv6304221copy number variation1nstd186human GRCh37 chr11: 3,824,458-3,825,241 , GRCh38.p12 chr11: 3,803,228-3,804,011 PGAP2
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6247705mobile element insertion1nstd215human GRCh38 chr11: 3,802,090-3,802,090 , GRCh37.p13 chr11: 3,823,320-3,823,320 PGAP2
    nsv6144195copy number variation1nstd206human GRCh38 chr11: 3,804,000-3,824,000 , GRCh37.p13 chr11: 3,825,230-3,845,230 PGAP2
    nsv6132264copy number variation1nstd213human GRCh37 chr11: 3,450,000-4,110,001 , GRCh38.p12 chr11: 3,428,770-4,088,771 RHOG, ART1, 23 more genes
    nsv6082805insertion1nstd212human GRCh38 chr11: 3,798,950-3,798,950 , GRCh37.p13 chr11: 3,820,180-3,820,180 PGAP2
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 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