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 285

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126355insertion1nstd186human GRCh37 chr5: 6,321,655-6,321,655 , GRCh38.p12 chr5: 6,321,542-6,321,542 LINC02145
    nsv5966817insertion1nstd209human GRCh38 chr5: 6,321,538-6,321,538 , GRCh37.p13 chr5: 6,321,651-6,321,651 LINC02145
    nsv5960774insertion1nstd209human GRCh38 chr5: 6,313,794-6,313,794 , GRCh37.p13 chr5: 6,313,907-6,313,907 LINC02145
    nsv5949263insertion1nstd209human GRCh38 chr5: 6,322,207-6,322,207 , GRCh37.p13 chr5: 6,322,320-6,322,320 LINC02145
    nsv5905818copy number variation1nstd209human GRCh38 chr5: 6,313,933-6,314,170 , GRCh37.p13 chr5: 6,314,046-6,314,283 LINC02145
    nsv5904269copy number variation1nstd209human GRCh38 chr5: 6,322,614-6,322,673 , GRCh37.p13 chr5: 6,322,727-6,322,786 LINC02145
    nsv5902460copy number variation1nstd209human GRCh38 chr5: 6,313,771-6,313,831 , GRCh37.p13 chr5: 6,313,884-6,313,944 LINC02145
    nsv5893608copy number variation1nstd209human GRCh38 chr5: 6,322,094-6,322,150 , GRCh37.p13 chr5: 6,322,207-6,322,263 LINC02145
    nsv5643782insertion1nstd207human GRCh38 chr5: 6,321,538-6,321,538 , GRCh37.p13 chr5: 6,321,651-6,321,651 LINC02145
    nsv5637268insertion1nstd207human GRCh38 chr5: 6,313,794-6,313,794 , GRCh37.p13 chr5: 6,313,907-6,313,907 LINC02145
    nsv5626207insertion1nstd207human GRCh38 chr5: 6,322,207-6,322,207 , GRCh37.p13 chr5: 6,322,320-6,322,320 LINC02145
    nsv5541115insertion1nstd206human GRCh38 chr5: 6,322,207-6,322,242 , GRCh37.p13 chr5: 6,322,320-6,322,355 LINC02145
    nsv5537525insertion1nstd206human GRCh38 chr5: 6,321,542-6,321,542 , GRCh37.p13 chr5: 6,321,655-6,321,655 LINC02145
    nsv5389186copy number variation2nstd186human GRCh37 chr5: 6,322,222-6,322,413 , GRCh38.p12 chr5: 6,322,109-6,322,300 LINC02145
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5377850translocation1nstd200human GRCh38 chr5: 6,314,771-6,314,771 , GRCh38 chr5: 6,314,836-6,314,836 , GRCh37.p13 chr5: 6,314,884-6,314,884 , GRCh37.p13 chr5: 6,314,949-6,314,949 LINC02145
    nsv4946339copy number variation1nstd200human GRCh38 chr5: 6,325,100-6,327,825 , GRCh37.p13 chr5: 6,325,213-6,327,938 LINC02145
    nsv4946338copy number variation1nstd200human GRCh38 chr5: 6,306,635-6,311,737 , GRCh37.p13 chr5: 6,306,748-6,311,850 LINC02145
    nsv4944334copy number variation1nstd200human GRCh38 chr5: 6,322,109-6,322,300 , GRCh37.p13 chr5: 6,322,222-6,322,413 LINC02145
    nsv4794882copy number variation1nstd200human GRCh37 chr5: 6,322,222-6,322,413 , GRCh38.p12 chr5: 6,322,109-6,322,300 LINC02145
    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