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 192

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122339copy number variation1nstd186human GRCh37 chr11: 49,425,097-49,425,416 , GRCh38.p12 chr11: 49,403,545-49,403,864 TYRL
    nsv5975160insertion1nstd209human GRCh38 chr11: 49,403,541-49,403,541 , GRCh37.p13 chr11: 49,425,093-49,425,093 TYRL
    nsv5972446insertion1nstd209human GRCh38 chr11: 49,406,768-49,406,768 , GRCh37.p13 chr11: 49,428,320-49,428,320 CBX3P8, TYRL
    nsv5919272copy number variation1nstd209human GRCh38 chr11: 48,727,127-55,124,866 , GRCh37.p13 chr11: 48,748,679-54,892,342 , OR4C50P, 54 more genes
    nsv5912495copy number variation1nstd209human GRCh38 chr11: 49,403,529-49,403,863 , GRCh37.p13 chr11: 49,425,081-49,425,415 TYRL
    nsv5861383copy number variation1nstd209human GRCh38 chr11: 49,383,883-49,406,477 , GRCh37.p13 chr11: 49,405,435-49,428,029 CBX3P8, TYRL
    nsv5660184insertion1nstd207human GRCh38 chr11: 49,406,805-49,406,805 , GRCh37.p13 chr11: 49,428,357-49,428,357 CBX3P8, TYRL
    nsv5659908insertion1nstd207human GRCh38 chr11: 49,406,092-49,406,092 , GRCh37.p13 chr11: 49,427,644-49,427,644 CBX3P8, TYRL
    nsv5659033insertion1nstd207human GRCh38 chr11: 49,408,931-49,408,931 , GRCh37.p13 chr11: 49,430,483-49,430,483 TYRL
    nsv5652291insertion1nstd207human GRCh38 chr11: 49,406,787-49,406,787 , GRCh37.p13 chr11: 49,428,339-49,428,339 CBX3P8, TYRL
    nsv5598569copy number variation1nstd207human GRCh38 chr11: 49,406,739-49,406,840 , GRCh37.p13 chr11: 49,428,291-49,428,392 TYRL, CBX3P8
    nsv5588419copy number variation1nstd207human GRCh38 chr11: 49,403,529-49,403,863 , GRCh37.p13 chr11: 49,425,081-49,425,415 TYRL
    nsv5556979sequence alteration1nstd206human GRCh38 chr11: 48,970,398-49,816,253 , GRCh37.p13 chr11: 48,991,950-49,837,805 , TRIM53CP, 15 more genes
    nsv5511914copy number variation1nstd206human GRCh38 chr11: 49,403,545-49,403,864 , GRCh37.p13 chr11: 49,425,097-49,425,416 TYRL
    nsv5382053mobile element deletion2nstd186human GRCh37 chr11: 49,425,097-49,425,416 , GRCh38.p12 chr11: 49,403,545-49,403,864 TYRL
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5279564copy number variation1nstd204human GRCh38.p13 chr11: 49,403,501-49,403,900 , GRCh37.p13 chr11: 49,425,053-49,425,452 TYRL
    nsv5204994mobile element deletion1nstd204human GRCh38.p13 chr11: 49,403,302-49,404,068 , GRCh37.p13 chr11: 49,424,854-49,425,620 TYRL
    nsv4984628copy number variation1nstd200human GRCh38 chr11: 49,412,113-49,444,569 , GRCh37.p13 chr11: 49,433,665-49,466,121 LOC653698, TYRL
    nsv4984627copy number variation1nstd200human GRCh38 chr11: 49,410,704-49,425,270 , GRCh37.p13 chr11: 49,432,256-49,446,822 TYRL
    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