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 106

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070306inversion1nstd229human GRCh38 chr11: 13,396,389-14,573,064 , GRCh37.p13 chr11: 13,417,936-14,594,610 LOC105376670, RRAS2, 15 more genes
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6910047copy number variation1nstd229human GRCh38 chr11: 13,914,535-13,930,428 , GRCh37.p13 chr11: 13,936,082-13,951,975 LINC02683
    nsv6908568copy number variation1nstd229human GRCh38 chr11: 13,921,341-13,921,392 , GRCh37.p13 chr11: 13,942,888-13,942,939 LINC02683
    nsv6902578copy number variation1nstd229human GRCh38 chr11: 13,892,666-14,075,666 , GRCh37.p13 chr11: 13,963,464-14,097,213 , GRCh37.p13 chr11|NW_003871075.1: 1-133,750 LINC02683, RNA5SP331, 1 more genes
    nsv6901514copy number variation1nstd229human GRCh38 chr11: 13,883,727-13,998,118 , GRCh37.p13 chr11: 13,905,274-13,963,463 SPON1, LINC02683, 1 more genes
    nsv6620828copy number variation1nstd224human GRCh37 chr11: 13,814,730-14,542,577 , GRCh38.p12 chr11: 13,793,183-14,521,031 PSMA1, RNU7-49P, 9 more genes
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6437879copy number variation1nstd223human GRCh38 chr11: 13,914,259-13,921,107 , GRCh37.p13 chr11: 13,935,806-13,942,654 LINC02683
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6131917copy number variation1nstd213human GRCh37 chr11: 13,690,000-14,110,001 , GRCh38.p12 chr11: 13,668,453-14,088,455 SPON1, FAR1, 6 more genes
    nsv5919380copy number variation1nstd209human GRCh38 chr11: 13,921,341-13,921,390 , GRCh37.p13 chr11: 13,942,888-13,942,937 LINC02683
    nsv5727218mobile element insertion2nstd211human GRCh38 chr11: 13,922,591-13,922,591 , GRCh37.p13 chr11: 13,944,138-13,944,138 LINC02683
    nsv5595818copy number variation1nstd207human GRCh38 chr11: 13,921,340-13,921,389 , GRCh37.p13 chr11: 13,942,887-13,942,936 LINC02683
    nsv5560678mobile element insertion1nstd206human GRCh38 chr11: 13,922,591-13,922,642 , GRCh37.p13 chr11: 13,944,138-13,944,189 LINC02683
    nsv5502519copy number variation1nstd206human GRCh38 chr11: 13,921,341-13,921,392 , GRCh37.p13 chr11: 13,942,888-13,942,939 LINC02683
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5198866mobile element insertion1nstd203human GRCh38 chr11: 13,922,579-13,922,591 , GRCh37.p13 chr11: 13,944,126-13,944,138 LINC02683
    nsv5198536mobile element insertion1nstd203human GRCh38 chr11: 13,922,578-13,922,591 , GRCh37.p13 chr11: 13,944,125-13,944,138 LINC02683
    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