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 366

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5895104copy number variation1nstd209human GRCh38 chr5: 131,280,923-131,282,654 , GRCh37.p13 chr5: 130,616,616-130,618,347 CDC42SE2
    nsv5841659copy number variation1nstd209human GRCh38 chr5: 131,280,941-131,282,690 , GRCh37.p13 chr5: 130,616,634-130,618,383 CDC42SE2
    nsv5722774mobile element insertion1nstd211human GRCh38 chr5: 131,315,225-131,315,225 , GRCh37.p13 chr5: 130,650,918-130,650,918 CDC42SE2
    nsv5717745mobile element insertion2nstd211human GRCh38 chr5: 131,391,345-131,391,345 , GRCh37.p13 chr5: 130,727,038-130,727,038 CDC42SE2
    nsv5716096mobile element insertion1nstd211human GRCh38 chr5: 131,315,242-131,315,242 , GRCh37.p13 chr5: 130,650,935-130,650,935 CDC42SE2
    nsv5694075mobile element insertion1nstd211human GRCh38 chr5: 131,266,955-131,266,955 , GRCh37.p13 chr5: 130,602,648-130,602,648 CDC42SE2
    nsv5690973mobile element insertion2nstd211human GRCh38 chr5: 131,324,489-131,324,489 , GRCh37.p13 chr5: 130,660,182-130,660,182 CDC42SE2
    nsv5674490mobile element insertion1nstd211human GRCh38 chr5: 131,266,954-131,266,954 , GRCh37.p13 chr5: 130,602,647-130,602,647 CDC42SE2
    nsv5636204insertion2nstd207human GRCh38 chr5: 131,278,741-131,278,741 , GRCh37.p13 chr5: 130,614,434-130,614,434 CDC42SE2
    nsv5467357copy number variation1nstd206human GRCh38 chr5: 131,279,631-131,281,922 , GRCh37.p13 chr5: 130,615,324-130,617,615 CDC42SE2
    nsv5464448copy number variation1nstd206human GRCh38 chr5: 131,275,300-131,282,369 , GRCh37.p13 chr5: 130,610,993-130,618,062 CDC42SE2
    nsv5460551copy number variation1nstd206human GRCh38 chr5: 131,292,308-131,292,658 , GRCh37.p13 chr5: 130,628,001-130,628,351 CDC42SE2
    nsv5456611copy number variation1nstd206human GRCh38 chr5: 131,392,374-131,392,466 , GRCh37.p13 chr5: 130,728,067-130,728,159 CDC42SE2, LOC105379173
    nsv5454172copy number variation1nstd206human GRCh38 chr5: 131,304,822-131,306,320 , GRCh37.p13 chr5: 130,640,515-130,642,013 CDC42SE2
    nsv5454128copy number variation1nstd206human GRCh38 chr5: 131,365,163-131,368,146 , GRCh37.p13 chr5: 130,700,856-130,703,839 CDC42SE2
    nsv5403880mobile element insertion1nstd206human GRCh38 chr5: 131,324,489-131,324,540 , GRCh37.p13 chr5: 130,660,182-130,660,233 CDC42SE2
    nsv5378060translocation1nstd200human GRCh38 chr5: 131,359,207-131,359,207 , GRCh38 chr5: 131,316,144-131,316,144 , GRCh37.p13 chr5: 130,651,837-130,651,837 , GRCh37.p13 chr5: 130,694,900-130,694,900 CDC42SE2
    nsv5378059translocation1nstd200human GRCh38 chr5: 131,306,320-131,306,320 , GRCh38 chr5: 131,304,822-131,304,822 , GRCh37.p13 chr5: 130,640,515-130,640,515 , GRCh37.p13 chr5: 130,642,013-130,642,013 CDC42SE2
    nsv5375270translocation1nstd200human GRCh38 chr2: 39,390,090-39,390,090 , GRCh38 chr5: 131,315,975-131,315,975 , GRCh37.p13 chr2: 39,617,231-39,617,231 , GRCh37.p13 chr5: 130,651,668-130,651,668 MAP4K3, CDC42SE2
    nsv5368939translocation1nstd200human GRCh38 chr16: 69,753,058-69,753,058 , GRCh38 chr5: 131,365,894-131,365,894 , GRCh37.p13 chr16: 69,786,961-69,786,961 , GRCh37.p13 chr5: 130,701,587-130,701,587 CDC42SE2, NOB1
    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