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 225

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075545inversion1nstd229human GRCh38 chr11: 37,743,348-39,275,230 , GRCh37.p13 chr11: 37,764,898-39,296,780 LOC101928563, RPL18P8, 7 more genes
    nsv7067849inversion1nstd229human GRCh38 chr11: 37,941,781-37,945,506 , GRCh37.p13 chr11: 37,963,331-37,967,056 LINC02760
    nsv7063681inversion1nstd229human GRCh38 chr11: 37,702,267-38,808,319 , GRCh37.p13 chr11: 37,723,817-38,829,869 LINC02759, DNAAF11P1, 5 more genes
    nsv7063669inversion1nstd229human GRCh38 chr11: 37,937,897-37,942,167 , GRCh37.p13 chr11: 37,959,447-37,963,717 LINC02760
    nsv6915173copy number variation1nstd229human GRCh38 chr11: 37,940,801-37,945,100 , GRCh37.p13 chr11: 37,962,351-37,966,650 LINC02760
    nsv6912062copy number variation1nstd229human GRCh38 chr11: 37,727,568-38,107,322 , GRCh37.p13 chr11: 37,749,118-38,128,872 LINC02760
    nsv6909522copy number variation1nstd229human GRCh38 chr11: 37,934,378-38,091,301 , GRCh37.p13 chr11: 37,955,928-38,112,851 LINC02760
    nsv6907405copy number variation1nstd229human GRCh38 chr11: 37,906,048-37,968,611 , GRCh37.p13 chr11: 37,927,598-37,990,161 LINC02760
    nsv6906214copy number variation1nstd229human GRCh38 chr11: 37,947,399-37,968,666 , GRCh37.p13 chr11: 37,968,949-37,990,216 LINC02760
    nsv6898113copy number variation1nstd229human GRCh38 chr11: 37,940,512-37,940,820 , GRCh37.p13 chr11: 37,962,062-37,962,370 LINC02760
    nsv6638023copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766 THEM7P, LOC105376624, 92 more genes
    nsv6621162copy number variation1nstd224human GRCh37 chr11: 37,768,477-38,031,231 , GRCh38.p12 chr11: 37,746,927-38,009,681 LINC02760
    nsv6474771copy number variation1nstd223human GRCh38 chr11: 37,940,495-37,940,820 , GRCh37.p13 chr11: 37,962,045-37,962,370 LINC02760
    nsv6471962copy number variation1nstd223human GRCh38 chr11: 37,947,730-37,948,383 , GRCh37.p13 chr11: 37,969,280-37,969,933 LINC02760
    nsv6464659copy number variation1nstd223human GRCh38 chr11: 37,834,858-38,219,583 , GRCh37.p13 chr11: 37,856,408-38,241,133 LOC105376634, DNAAF11P1, 1 more genes
    nsv6463468copy number variation1nstd223human GRCh38 chr11: 37,941,855-37,942,816 , GRCh37.p13 chr11: 37,963,405-37,964,366 LINC02760
    nsv6463044copy number variation1nstd223human GRCh38 chr11: 37,930,327-38,067,751 , GRCh37.p13 chr11: 37,951,877-38,089,301 LINC02760
    nsv6459961copy number variation1nstd223human GRCh38 chr11: 37,727,568-38,107,320 , GRCh37.p13 chr11: 37,749,118-38,128,870 LINC02760
    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
    nsv6132176copy number variation1nstd213human GRCh37 chr11: 37,650,000-38,260,001 , GRCh38.p12 chr11: 37,628,450-38,238,451 RPL7AP56, DNAAF11P1, 2 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