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 578

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126671insertion1nstd186human GRCh37 chr10: 126,787,175-126,787,216 , GRCh38.p12 chr10: 125,098,606-125,098,647 CTBP2
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5920193copy number variation1nstd209human GRCh38 chr10: 125,029,676-125,031,829 , GRCh37.p13 chr10: 126,718,245-126,720,398 MIR4296, CTBP2
    nsv5860281copy number variation1nstd209human GRCh38 chr10: 125,029,638-125,031,875 , GRCh37.p13 chr10: 126,718,207-126,720,444 CTBP2, MIR4296
    nsv5730737mobile element insertion1nstd211human GRCh38 chr10: 125,010,395-125,010,395 , GRCh37.p13 chr10: 126,698,964-126,698,964 CTBP2
    nsv5561158mobile element insertion1nstd206human GRCh38 chr10: 125,010,395-125,010,446 , GRCh37.p13 chr10: 126,698,964-126,699,015 CTBP2
    nsv5549045insertion1nstd206human GRCh38 chr10: 125,098,624-125,098,712 , GRCh37.p13 chr10: 126,787,193-126,787,281 CTBP2
    nsv5546737insertion1nstd206human GRCh38 chr10: 125,098,606-125,098,647 , GRCh37.p13 chr10: 126,787,175-126,787,216 CTBP2
    nsv5513046copy number variation1nstd206human GRCh38 chr10: 125,032,503-125,032,575 , GRCh37.p13 chr10: 126,721,072-126,721,144 CTBP2, MIR4296
    nsv5511272copy number variation1nstd206human GRCh38 chr10: 125,139,737-125,139,880 , GRCh37.p13 chr10: 126,828,306-126,828,449 CTBP2
    nsv5506929copy number variation1nstd206human GRCh38 chr10: 125,008,360-125,008,652 , GRCh37.p13 chr10: 126,696,929-126,697,221 CTBP2
    nsv5503395copy number variation1nstd206human GRCh38 chr10: 125,031,186-125,037,069 , GRCh37.p13 chr10: 126,719,755-126,725,638 CTBP2, MIR4296
    nsv5501007copy number variation1nstd206human GRCh38 chr10: 125,150,877-125,151,630 , GRCh37.p13 chr10: 126,839,446-126,840,199 CTBP2
    nsv5498709copy number variation1nstd206human GRCh38 chr10: 125,102,763-125,108,538 , GRCh37.p13 chr10: 126,791,332-126,797,107 CTBP2
    nsv5494090copy number variation1nstd206human GRCh38 chr10: 124,987,934-124,988,002 , GRCh37.p13 chr10: 126,676,503-126,676,571 CTBP2, ZRANB1
    nsv5373319translocation1nstd200human GRCh38 chr10: 125,113,792-125,113,792 , GRCh38 chr10: 125,114,131-125,114,131 , GRCh37.p13 chr10: 126,802,700-126,802,700 , GRCh37.p13 chr10: 126,802,361-126,802,361 CTBP2
    nsv5373318translocation1nstd200human GRCh38 chr10: 125,113,272-125,113,272 , GRCh38 chr10: 125,114,133-125,114,133 , GRCh37.p13 chr10: 126,801,841-126,801,841 , GRCh37.p13 chr10: 126,802,702-126,802,702 CTBP2
    nsv5354563translocation1nstd200human GRCh38 chr10: 124,987,934-124,987,934 , GRCh38 chr10: 124,988,002-124,988,002 , GRCh37.p13 chr10: 126,676,571-126,676,571 , GRCh37.p13 chr10: 126,676,503-126,676,503 ZRANB1, CTBP2
    nsv5333504translocation1nstd200human GRCh37 chr7|GL000195.1: 11-11 , GRCh37 chr10: 126,678,260-126,678,260 , GRCh38.p12 chr10: 124,989,691-124,989,691 CTBP2
    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