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 507

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7074105inversion1nstd229human GRCh38 chr10: 17,945,641-22,801,235 , GRCh37.p13 chr10: 18,252,931-23,090,164 UBE2V2P1, LOC105376450, 62 more genes
    nsv7073711inversion1nstd229human GRCh38 chr10: 21,546,067-21,546,125 , GRCh37.p13 chr10: 21,834,996-21,835,054 MLLT10
    nsv7063218inversion1nstd229human GRCh38 chr10: 21,664,813-22,447,089 , GRCh37.p13 chr10: 21,953,742-22,736,018 PSME2P6, LOC107984214, 16 more genes
    nsv7061629inversion1nstd229human GRCh38 chr10: 21,647,192-21,851,842 , GRCh37.p13 chr10: 21,936,121-22,140,771 MLLT10, RN7SKP219, 3 more genes
    nsv7059332inversion1nstd229human GRCh38 chr10: 21,554,409-21,554,490 , GRCh37.p13 chr10: 21,843,338-21,843,419 MLLT10
    nsv6896967copy number variation1nstd229human GRCh38 chr10: 21,658,101-21,791,900 , GRCh37.p13 chr10: 21,947,030-22,080,829 RNU6-1141P, DNAJC1, 3 more genes
    nsv6896154copy number variation1nstd229human GRCh38 chr10: 21,640,601-21,648,400 , GRCh37.p13 chr10: 21,929,530-21,937,329 MLLT10
    nsv6895880copy number variation1nstd229human GRCh38 chr10: 21,682,268-21,688,888 , GRCh37.p13 chr10: 21,971,197-21,977,817 MLLT10
    nsv6894767copy number variation1nstd229human GRCh38 chr10: 21,613,648-21,613,731 , GRCh37.p13 chr10: 21,902,577-21,902,660 MLLT10
    nsv6894485copy number variation1nstd229human GRCh38 chr10: 21,633,909-21,634,051 , GRCh37.p13 chr10: 21,922,838-21,922,980 MLLT10
    nsv6893333copy number variation1nstd229human GRCh38 chr10: 20,964,833-22,078,565 , GRCh37.p13 chr10: 21,253,762-22,367,494 RN7SKP219, RN7SKP37, 19 more genes
    nsv6891034copy number variation1nstd229human GRCh38 chr10: 19,515,837-21,850,350 , GRCh37.p13 chr10: 19,804,766-22,139,279 LOC107984214, LOC101928834, 31 more genes
    nsv6889788copy number variation1nstd229human GRCh38 chr10: 21,543,009-21,549,713 , GRCh37.p13 chr10: 21,831,938-21,838,642 MLLT10
    nsv6887161copy number variation1nstd229human GRCh38 chr10: 21,722,444-21,722,808 , GRCh37.p13 chr10: 22,011,373-22,011,737 MLLT10
    nsv6886531copy number variation1nstd229human GRCh38 chr10: 21,647,101-21,664,800 , GRCh37.p13 chr10: 21,936,030-21,953,729 RNU6-1141P, MLLT10
    nsv6886442copy number variation1nstd229human GRCh38 chr10: 21,677,100-21,680,521 , GRCh37.p13 chr10: 21,966,029-21,969,450 MLLT10
    nsv6885780copy number variation1nstd229human GRCh38 chr10: 21,706,484-21,710,465 , GRCh37.p13 chr10: 21,995,413-21,999,394 MLLT10
    nsv6884789copy number variation1nstd229human GRCh38 chr10: 21,577,760-21,579,853 , GRCh37.p13 chr10: 21,866,689-21,868,782 MLLT10, LOC100422524
    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