U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 378

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6883389copy number variation1nstd229human GRCh38 chr11: 222,093-232,414 , GRCh37.p13 chr11: 222,093-232,414 SIRT3
    nsv6890745copy number variation1nstd229human GRCh38 chr11: 222,848-223,272 , GRCh37.p13 chr11: 222,848-223,272 SIRT3
    nsv6892590copy number variation1nstd229human GRCh38 chr11: 221,871-221,904 , GRCh37.p13 chr11: 221,871-221,904 SIRT3
    nsv7141054copy number variation1nstd232human GRCh37.p13 chr11: 223,976-224,047 , GRCh38.p12 chr11: 223,976-224,047 SIRT3
    nsv4645943copy number variation1nstd186human GRCh37 chr11: 223,794-224,002 , GRCh38.p12 chr11: 223,794-224,002 SIRT3
    nsv5391406copy number variation1nstd186human GRCh37 chr11: 223,856-224,002 , GRCh38.p12 chr11: 223,856-224,002 SIRT3
    nsv6188778copy number variation1nstd214human GRCh38 chr11: 223,786-224,001 , GRCh37.p13 chr11: 223,786-224,001 SIRT3
    nsv6204968copy number variation1nstd214human GRCh38 chr11: 223,844-224,047 , GRCh37.p13 chr11: 223,844-224,047 SIRT3
    nsv6201470copy number variation1nstd214human GRCh38 chr11: 223,786-223,929 , GRCh37.p13 chr11: 223,786-223,929 SIRT3
    nsv6190586copy number variation1nstd214human GRCh38 chr11: 223,832-223,975 , GRCh37.p13 chr11: 223,832-223,975 SIRT3
    nsv6271053copy number variation1nstd214human GRCh38 chr11: 223,976-224,047 , GRCh37.p13 chr11: 223,976-224,047 SIRT3
    nsv6194525copy number variation1nstd214human GRCh38 chr11: 223,940-224,011 , GRCh37.p13 chr11: 223,940-224,011 SIRT3
    nsv6036187copy number variation1nstd212human GRCh38 chr11: 220,809-220,958 , GRCh37.p13 chr11: 220,809-220,958 SIRT3
    nsv6032305copy number variation1nstd212human GRCh38 chr11: 223,787-223,936 , GRCh37.p13 chr11: 223,787-223,936 SIRT3
    nsv6028420copy number variation1nstd212human GRCh38 chr11: 220,892-220,957 , GRCh37.p13 chr11: 220,892-220,957 SIRT3
    nsv4743280copy number variation1nstd199human GRCh37 chr11: 223,837-223,982 , GRCh38.p12 chr11: 223,837-223,982 SIRT3
    nsv5318867copy number variation1nstd204human GRCh38.p13 chr11: 223,686-224,078 , GRCh37.p13 chr11: 223,686-224,078 SIRT3
    nsv5586438copy number variation1nstd207human GRCh38 chr11: 223,786-224,001 , GRCh37.p13 chr11: 223,786-224,001 SIRT3
    nsv5593651copy number variation1nstd207human GRCh38 chr11: 220,768-220,918 , GRCh37.p13 chr11: 220,768-220,918 SIRT3
    nsv5301545copy number variation1nstd204human GRCh38.p13 chr11: 223,847-224,011 , GRCh37.p13 chr11: 223,847-224,011 SIRT3
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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