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 153

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098966copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 61,131,991-61,135,394 , GRCh38.p12 chr11: 61,364,519-61,367,922 TMEM138
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6911462copy number variation1nstd229human GRCh38 chr11: 61,372,725-61,381,161 , GRCh37.p13 chr11: 61,140,197-61,148,633 TMEM138
    nsv6909765copy number variation1nstd229human GRCh38 chr11: 61,334,410-61,379,854 , GRCh37.p13 chr11: 61,101,882-61,147,326 CYB561A3, TMEM138, 1 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6904143copy number variation1nstd229human GRCh38 chr11: 61,370,493-61,370,969 , GRCh37.p13 chr11: 61,137,965-61,138,441 TMEM138
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6470541copy number variation1nstd223human GRCh38 chr11: 61,372,719-61,381,165 , GRCh37.p13 chr11: 61,140,191-61,148,637 TMEM138
    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
    nsv6309372copy number variation1nstd102humanPathogenic GRCh37 chr11: 61,133,497-61,133,708 , GRCh38.p12 chr11: 61,366,025-61,366,236 TMEM138
    nsv6293565mobile element insertion1nstd186human GRCh37 chr11: 61,141,198-61,141,249 , GRCh38.p12 chr11: 61,373,726-61,373,777 TMEM138
    nsv6248118mobile element insertion1nstd215human GRCh38 chr11: 61,377,742-61,377,742 , GRCh37.p13 chr11: 61,145,214-61,145,214 TMEM138
    nsv6089825insertion1nstd212human GRCh38 chr11: 61,377,729-61,377,729 , GRCh37.p13 chr11: 61,145,201-61,145,201 TMEM138
    nsv5972765insertion1nstd209human GRCh38 chr11: 61,377,729-61,377,729 , GRCh37.p13 chr11: 61,145,201-61,145,201 TMEM138
    nsv5913316copy number variation1nstd209human GRCh38 chr11: 61,358,555-61,360,806 , GRCh37.p13 chr11: 61,126,027-61,128,278 TMEM138, CYB561A3
    nsv5910842copy number variation1nstd209human GRCh38 chr11: 61,364,834-61,365,126 , GRCh37.p13 chr11: 61,132,306-61,132,598 TMEM138
    nsv5862465copy number variation1nstd209human GRCh38 chr11: 61,358,562-61,360,761 , GRCh37.p13 chr11: 61,126,034-61,128,233 CYB561A3, TMEM138
    nsv5716447mobile element insertion1nstd211human GRCh38 chr11: 61,372,973-61,372,973 , GRCh37.p13 chr11: 61,140,445-61,140,445 TMEM138
    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