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 299

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896558copy number variation1nstd209human GRCh38 chr3: 113,760,464-113,762,303 , GRCh37.p13 chr3: 113,479,311-113,481,150 ATP6V1A
    nsv5896076copy number variation1nstd209human GRCh38 chr3: 113,786,634-113,786,724 , GRCh37.p13 chr3: 113,505,481-113,505,571 ATP6V1A
    nsv5686945mobile element insertion2nstd211human GRCh38 chr3: 113,791,409-113,791,409 , GRCh37.p13 chr3: 113,510,256-113,510,256 ATP6V1A
    nsv5571308copy number variation1nstd207human GRCh38 chr3: 113,761,737-113,762,151 , GRCh37.p13 chr3: 113,480,584-113,480,998 ATP6V1A
    nsv5571117copy number variation1nstd207human GRCh38 chr3: 113,782,545-113,782,602 , GRCh37.p13 chr3: 113,501,392-113,501,449 ATP6V1A
    nsv5541940insertion1nstd206human GRCh38 chr3: 113,782,610-113,782,636 , GRCh37.p13 chr3: 113,501,457-113,501,483 ATP6V1A
    nsv5537149insertion1nstd206human GRCh38 chr3: 113,782,516-113,782,561 , GRCh37.p13 chr3: 113,501,363-113,501,408 ATP6V1A
    nsv5448515copy number variation1nstd206human GRCh38 chr3: 113,793,719-113,793,872 , GRCh37.p13 chr3: 113,512,566-113,512,719 ATP6V1A
    nsv5442912copy number variation1nstd206human GRCh38 chr3: 113,782,545-113,782,613 , GRCh37.p13 chr3: 113,501,392-113,501,460 ATP6V1A
    nsv5435031copy number variation1nstd206human GRCh38 chr3: 113,760,464-113,762,334 , GRCh37.p13 chr3: 113,479,311-113,481,181 ATP6V1A
    nsv5412467mobile element insertion1nstd206human GRCh38 chr3: 113,791,409-113,791,460 , GRCh37.p13 chr3: 113,510,256-113,510,307 ATP6V1A
    nsv5346426translocation1nstd200human GRCh38 chr3: 113,751,304-113,751,304 , GRCh38 chr3: 113,766,494-113,766,494 , GRCh37.p13 chr3: 113,470,151-113,470,151 , GRCh37.p13 chr3: 113,485,341-113,485,341 ATP6V1A
    nsv5240055copy number variation1nstd204human GRCh38.p13 chr3: 113,761,801-113,762,200 , GRCh37.p13 chr3: 113,480,648-113,481,047 ATP6V1A
    nsv5089797mobile element insertion1nstd203human GRCh38 chr3: 113,753,669-113,753,710 , GRCh37.p13 chr3: 113,472,516-113,472,557 ATP6V1A
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919600copy number variation1nstd200human GRCh38 chr3: 113,806,627-113,808,389 , GRCh37.p13 chr3: 113,525,474-113,527,236 ATP6V1A
    nsv4919599copy number variation1nstd200human GRCh38 chr3: 113,756,612-113,756,676 , GRCh37.p13 chr3: 113,475,459-113,475,523 ATP6V1A
    nsv4914656copy number variation1nstd200human GRCh38 chr3: 113,760,463-113,761,935 , GRCh37.p13 chr3: 113,479,310-113,480,782 ATP6V1A
    nsv4806804copy number variation1nstd200human GRCh37 chr3: 113,470,151-113,485,341 , GRCh38.p12 chr3: 113,751,304-113,766,494 ATP6V1A
    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