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 214

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6910666copy number variation1nstd229human GRCh38 chr11: 57,756,748-57,761,148 , GRCh37.p13 chr11: 57,524,220-57,528,620 TMX2-CTNND1, CTNND1
    nsv6907639copy number variation1nstd229human GRCh38 chr11: 57,796,993-57,801,727 , GRCh37.p13 chr11: 57,564,465-57,569,199 CTNND1, TMX2-CTNND1
    nsv6899102copy number variation1nstd229human GRCh38 chr11: 57,784,067-57,790,218 , GRCh37.p13 chr11: 57,551,539-57,557,690 CTNND1, TMX2-CTNND1
    nsv6898452copy number variation1nstd229human GRCh38 chr11: 57,755,677-57,760,598 , GRCh37.p13 chr11: 57,523,149-57,528,070 TMX2-CTNND1, CTNND1
    nsv6589007inversion1nstd223human GRCh38 chr11: 57,810,506-57,810,796 , GRCh37.p13 chr11: 57,577,978-57,578,268 TMX2-CTNND1, CTNND1
    nsv6588985inversion1nstd223human GRCh38 chr11: 57,760,562-57,761,186 , GRCh37.p13 chr11: 57,528,034-57,528,658 CTNND1, TMX2-CTNND1
    nsv6473708copy number variation1nstd223human GRCh38 chr11: 57,756,724-57,760,697 , GRCh37.p13 chr11: 57,524,196-57,528,169 CTNND1, TMX2-CTNND1
    nsv6458984copy number variation1nstd223human GRCh38 chr11: 57,784,060-57,790,244 , GRCh37.p13 chr11: 57,551,532-57,557,716 TMX2-CTNND1, CTNND1
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6305139copy number variation1nstd186human GRCh37 chr11: 57,561,490-57,561,599 , GRCh38.p12 chr11: 57,794,018-57,794,127 CTNND1, TMX2-CTNND1
    nsv6291401copy number variation1nstd102humannot provided GRCh37 chr11: 57,112,299-57,871,866 , GRCh38.p12 chr11: 57,344,825-58,104,394 RN7SL605P, CLP1, 35 more genes
    nsv6132267copy number variation1nstd213human GRCh37 chr11: 57,560,000-57,780,001 , GRCh38.p12 chr11: 57,792,528-58,012,529 CTNND1, OR5BD1P, 5 more genes
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5914833copy number variation1nstd209human GRCh38 chr11: 57,776,396-57,777,043 , GRCh37.p13 chr11: 57,543,868-57,544,515 TMX2-CTNND1, CTNND1
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5672633copy number variation1nstd102humanPathogenic GRCh37 chr11: 57,471,510-57,564,464 , GRCh38.p12 chr11: 57,704,038-57,796,992 CTNND1, TMX2, 5 more genes
    nsv5672557copy number variation1nstd102humanPathogenic GRCh37 chr11: 57,558,951-57,583,780 , GRCh38.p12 chr11: 57,791,479-57,816,308 TMX2-CTNND1, CTNND1
    nsv5511343copy number variation1nstd206human GRCh38 chr11: 57,794,018-57,794,127 , GRCh37.p13 chr11: 57,561,490-57,561,599 CTNND1, TMX2-CTNND1
    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