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 510

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121524copy number variation1nstd186human GRCh37 chr10: 125,664,376-125,664,440 , GRCh38.p12 chr10: 123,904,860-123,904,924 LOC105378534, CPXM2
    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
    nsv5972575insertion1nstd209human GRCh38 chr10: 123,881,229-123,881,229 , GRCh37.p13 chr10: 125,640,745-125,640,745 CPXM2
    nsv5927171copy number variation1nstd209human GRCh38 chr10: 123,790,217-123,790,332 , GRCh37.p13 chr10: 125,549,733-125,549,848 CPXM2
    nsv5918840copy number variation1nstd209human GRCh38 chr10: 123,773,213-123,773,275 , GRCh37.p13 chr10: 125,532,729-125,532,791 CPXM2
    nsv5915364copy number variation1nstd209human GRCh38 chr10: 123,873,161-123,873,272 , GRCh37.p13 chr10: 125,632,677-125,632,788 CPXM2
    nsv5915251copy number variation1nstd209human GRCh38 chr10: 123,772,265-123,772,432 , GRCh37.p13 chr10: 125,531,781-125,531,948 CPXM2
    nsv5912379copy number variation1nstd209human GRCh38 chr10: 123,857,551-123,857,658 , GRCh37.p13 chr10: 125,617,067-125,617,174 CPXM2
    nsv5720555mobile element insertion1nstd211human GRCh38 chr10: 123,780,448-123,780,448 , GRCh37.p13 chr10: 125,539,964-125,539,964 CPXM2
    nsv5697237mobile element insertion2nstd211human GRCh38 chr10: 123,746,186-123,746,186 , GRCh37.p13 chr10: 125,505,702-125,505,702 CPXM2
    nsv5643666insertion1nstd207human GRCh38 chr10: 123,936,097-123,936,097 , GRCh37.p13 chr10: 125,695,613-125,695,613 CPXM2
    nsv5633099insertion1nstd207human GRCh38 chr10: 123,854,376-123,854,376 , GRCh37.p13 chr10: 125,613,892-125,613,892 CPXM2
    nsv5632925insertion2nstd207human GRCh38 chr10: 123,881,225-123,881,225 , GRCh37.p13 chr10: 125,640,741-125,640,741 CPXM2
    nsv5627252insertion2nstd207human GRCh38 chr10: 123,904,876-123,904,876 , GRCh37.p13 chr10: 125,664,392-125,664,392 CPXM2, LOC105378534
    nsv5603908copy number variation1nstd207human GRCh38 chr10: 123,790,217-123,790,332 , GRCh37.p13 chr10: 125,549,733-125,549,848 CPXM2
    nsv5596628copy number variation1nstd207human GRCh38 chr10: 123,773,213-123,773,275 , GRCh37.p13 chr10: 125,532,729-125,532,791 CPXM2
    nsv5593452copy number variation1nstd207human GRCh38 chr10: 123,873,161-123,873,272 , GRCh37.p13 chr10: 125,632,677-125,632,788 CPXM2
    nsv5586391copy number variation1nstd207human GRCh38 chr10: 123,857,542-123,857,649 , GRCh37.p13 chr10: 125,617,058-125,617,165 CPXM2
    nsv5561106mobile element insertion1nstd206human GRCh38 chr10: 123,780,448-123,780,499 , GRCh37.p13 chr10: 125,539,964-125,540,015 CPXM2
    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