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 495

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117425mobile element insertion1nstd186human GRCh37 chr16: 27,596,584-27,596,614 , GRCh38.p12 chr16: 27,585,263-27,585,293 KATNIP
    nsv5979412insertion1nstd209human GRCh38 chr16: 27,558,829-27,558,829 , GRCh37.p13 chr16: 27,570,150-27,570,150 KATNIP
    nsv5941151copy number variation1nstd209human GRCh38 chr16: 27,615,616-27,616,466 , GRCh37.p13 chr16: 27,626,937-27,627,787 KATNIP
    nsv5940701copy number variation1nstd209human GRCh38 chr16: 27,709,787-27,713,872 , GRCh37.p13 chr16: 27,721,108-27,725,193 LOC100128079, KATNIP
    nsv5936362copy number variation1nstd209human GRCh38 chr16: 27,575,793-27,576,016 , GRCh37.p13 chr16: 27,587,114-27,587,337 KATNIP
    nsv5934609copy number variation1nstd209human GRCh38 chr16: 27,778,073-27,778,531 , GRCh37.p13 chr16: 27,789,394-27,789,852 KATNIP
    nsv5883171copy number variation2nstd209human GRCh38 chr16: 27,709,761-27,710,990 , GRCh37.p13 chr16: 27,721,082-27,722,311 KATNIP, LOC100128079
    nsv5873554copy number variation1nstd209human GRCh38 chr16: 27,709,762-27,713,490 , GRCh37.p13 chr16: 27,721,083-27,724,811 LOC100128079, KATNIP
    nsv5724093mobile element insertion1nstd211human GRCh38 chr16: 27,635,873-27,635,873 , GRCh37.p13 chr16: 27,647,194-27,647,194 KATNIP
    nsv5710170mobile element insertion2nstd211human GRCh38 chr16: 27,558,844-27,558,844 , GRCh37.p13 chr16: 27,570,165-27,570,165 KATNIP
    nsv5709863mobile element insertion1nstd211human GRCh38 chr16: 27,585,293-27,585,293 , GRCh37.p13 chr16: 27,596,614-27,596,614 KATNIP
    nsv5708633mobile element insertion1nstd211human GRCh38 chr16: 27,616,919-27,616,919 , GRCh37.p13 chr16: 27,628,240-27,628,240 KATNIP
    nsv5707948mobile element insertion1nstd211human GRCh38 chr16: 27,662,072-27,662,072 , GRCh37.p13 chr16: 27,673,393-27,673,393 KATNIP
    nsv5662866insertion1nstd207human GRCh38 chr16: 27,713,641-27,713,641 , GRCh37.p13 chr16: 27,724,962-27,724,962 LOC100128079, KATNIP
    nsv5592818copy number variation1nstd207human GRCh38 chr16: 27,661,943-27,662,076 , GRCh37.p13 chr16: 27,673,264-27,673,397 KATNIP
    nsv5531657copy number variation1nstd206human GRCh38 chr16: 27,692,825-27,692,884 , GRCh37.p13 chr16: 27,704,146-27,704,205 KATNIP
    nsv5526315copy number variation1nstd206human GRCh38 chr16: 27,644,137-27,645,628 , GRCh37.p13 chr16: 27,655,458-27,656,949 KATNIP
    nsv5525193copy number variation1nstd206human GRCh38 chr16: 27,748,479-27,748,698 , GRCh37.p13 chr16: 27,759,800-27,760,019 KATNIP, LOC105371157
    nsv5523858copy number variation1nstd206human GRCh38 chr16: 27,554,273-27,559,844 , GRCh37.p13 chr16: 27,565,594-27,571,165 KATNIP
    nsv5523605copy number variation1nstd206human GRCh38 chr16: 27,778,077-27,778,532 , GRCh37.p13 chr16: 27,789,398-27,789,853 KATNIP
    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