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 643

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965696insertion1nstd209human GRCh38 chr9: 4,600,491-4,600,491 , GRCh37.p13 chr9: 4,600,491-4,600,491 SPATA6L
    nsv5960725insertion1nstd209human GRCh38 chr9: 4,661,749-4,661,749 , GRCh37.p13 chr9: 4,661,749-4,661,749 SPATA6L, PLPP6
    nsv5957468insertion1nstd209human GRCh38 chr9: 4,545,189-4,545,189 , GRCh37.p13 chr9: 4,545,189-4,545,189 SLC1A1, SPATA6L
    nsv5927284copy number variation1nstd209human GRCh38 chr9: 4,656,450-4,656,505 , GRCh37.p13 chr9: 4,656,450-4,656,505 SPATA6L
    nsv5921121copy number variation1nstd209human GRCh38 chr9: 4,628,117-4,629,380 , GRCh37.p13 chr9: 4,628,117-4,629,380 SPATA6L
    nsv5859286copy number variation1nstd209human GRCh38 chr9: 4,627,816-4,629,147 , GRCh37.p13 chr9: 4,627,816-4,629,147 SPATA6L
    nsv5858875copy number variation1nstd209human GRCh38 chr9: 4,604,731-4,608,888 , GRCh37.p13 chr9: 4,604,731-4,608,888 SPATA6L
    nsv5723131mobile element insertion2nstd211human GRCh38 chr9: 4,540,923-4,540,923 , GRCh37.p13 chr9: 4,540,923-4,540,923 SPATA6L, SLC1A1
    nsv5695744mobile element insertion1nstd211human GRCh38 chr9: 4,623,476-4,623,476 , GRCh37.p13 chr9: 4,623,476-4,623,476 SPATA6L
    nsv5695240mobile element insertion2nstd211human GRCh38 chr9: 4,642,718-4,642,718 , GRCh37.p13 chr9: 4,642,718-4,642,718 SPATA6L
    nsv5493058copy number variation1nstd206human GRCh38 chr9: 4,656,901-4,657,026 , GRCh37.p13 chr9: 4,656,901-4,657,026 SPATA6L
    nsv5491241copy number variation1nstd206human GRCh38 chr9: 4,656,030-4,656,361 , GRCh37.p13 chr9: 4,656,030-4,656,361 SPATA6L
    nsv5487167copy number variation1nstd206human GRCh38 chr9: 4,628,119-4,629,381 , GRCh37.p13 chr9: 4,628,119-4,629,381 SPATA6L
    nsv5481390copy number variation1nstd206human GRCh38 chr9: 4,665,105-4,665,415 , GRCh37.p13 chr9: 4,665,105-4,665,415 SPATA6L, PLPP6
    nsv5406812mobile element insertion1nstd206human GRCh38 chr9: 4,642,718-4,642,761 , GRCh37.p13 chr9: 4,642,718-4,642,761 SPATA6L
    nsv5405585mobile element insertion1nstd206human GRCh38 chr9: 4,606,370-4,606,421 , GRCh37.p13 chr9: 4,606,370-4,606,421 SPATA6L
    nsv5394978mobile element insertion1nstd206human GRCh38 chr9: 4,623,476-4,623,527 , GRCh37.p13 chr9: 4,623,476-4,623,527 SPATA6L
    nsv5381785copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,854,435-6,937,677 , GRCh38.p12 chr9: 2,854,435-6,937,677 GLIS3-AS1, RFX3-DT, 70 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5381702copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,029,023-5,300,444 , GRCh38.p12 chr9: 2,029,023-5,300,444 MTND5P36, MTND2P36, 53 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