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 369

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130129insertion1nstd186human GRCh37 chr19: 18,800,292-18,800,292 , GRCh38.p12 chr19: 18,689,482-18,689,482 CRTC1
    nsv6124653copy number variation1nstd186human GRCh37 chr19: 18,847,104-18,847,597 , GRCh38.p12 chr19: 18,736,294-18,736,787 CRTC1
    nsv5978286insertion1nstd209human GRCh38 chr19: 18,724,789-18,724,789 , GRCh37.p13 chr19: 18,835,599-18,835,599 CRTC1
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5974761insertion1nstd209human GRCh38 chr19: 18,686,221-18,686,221 , GRCh37.p13 chr19: 18,797,031-18,797,031 CRTC1
    nsv5972071insertion1nstd209human GRCh38 chr19: 18,713,546-18,713,546 , GRCh37.p13 chr19: 18,824,356-18,824,356 CRTC1
    nsv5970162insertion1nstd209human GRCh38 chr19: 18,689,482-18,689,482 , GRCh37.p13 chr19: 18,800,292-18,800,292 CRTC1
    nsv5947289copy number variation1nstd209human GRCh38 chr19: 18,779,636-18,779,979 , GRCh37.p13 chr19: 18,890,446-18,890,789 CRTC1
    nsv5947149copy number variation1nstd209human GRCh38 chr19: 18,727,833-18,728,616 , GRCh37.p13 chr19: 18,838,643-18,839,426 CRTC1
    nsv5942236copy number variation1nstd209human GRCh38 chr19: 18,733,038-18,733,139 , GRCh37.p13 chr19: 18,843,848-18,843,949 CRTC1
    nsv5941898copy number variation1nstd209human GRCh38 chr19: 18,736,294-18,736,784 , GRCh37.p13 chr19: 18,847,104-18,847,594 CRTC1
    nsv5727901mobile element insertion2nstd211human GRCh38 chr19: 18,751,223-18,751,223 , GRCh37.p13 chr19: 18,862,033-18,862,033 CRTC1
    nsv5696077mobile element insertion1nstd211human GRCh38 chr19: 18,686,238-18,686,238 , GRCh37.p13 chr19: 18,797,048-18,797,048 CRTC1
    nsv5661051insertion1nstd207human GRCh38 chr19: 18,724,789-18,724,789 , GRCh37.p13 chr19: 18,835,599-18,835,599 CRTC1
    nsv5648921insertion1nstd207human GRCh38 chr19: 18,689,482-18,689,482 , GRCh37.p13 chr19: 18,800,292-18,800,292 CRTC1
    nsv5562673mobile element insertion1nstd206human GRCh38 chr19: 18,751,237-18,751,274 , GRCh37.p13 chr19: 18,862,047-18,862,084 CRTC1
    nsv5538336insertion1nstd206human GRCh38 chr19: 18,689,482-18,689,482 , GRCh37.p13 chr19: 18,800,292-18,800,292 CRTC1
    nsv5530719copy number variation1nstd206human GRCh38 chr19: 18,779,636-18,779,985 , GRCh37.p13 chr19: 18,890,446-18,890,795 CRTC1
    nsv5527191copy number variation1nstd206human GRCh38 chr19: 18,725,013-18,725,079 , GRCh37.p13 chr19: 18,835,823-18,835,889 CRTC1
    nsv5525660copy number variation1nstd206human GRCh38 chr19: 18,722,949-18,723,622 , GRCh37.p13 chr19: 18,833,759-18,834,432 CRTC1
    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