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 338

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951605insertion1nstd209human GRCh38 chr3: 194,421,137-194,421,137 , GRCh37.p13 chr3: 194,141,866-194,141,866 ATP13A3
    nsv5906583copy number variation1nstd209human GRCh38 chr3: 194,400,435-194,401,191 , GRCh37.p13 chr3: 194,121,164-194,121,920 ATP13A3
    nsv5894645copy number variation1nstd209human GRCh38 chr3: 194,473,430-194,473,727 , GRCh37.p13 chr3: 194,194,159-194,194,456 ATP13A3
    nsv5890647copy number variation1nstd209human GRCh38 chr3: 194,436,762-194,436,812 , GRCh37.p13 chr3: 194,157,491-194,157,541 ATP13A3
    nsv5679675mobile element insertion2nstd211human GRCh38 chr3: 194,440,857-194,440,857 , GRCh37.p13 chr3: 194,161,586-194,161,586 ATP13A3
    nsv5678214mobile element insertion1nstd211human GRCh38 chr3: 194,411,538-194,411,538 , GRCh37.p13 chr3: 194,132,267-194,132,267 ATP13A3
    nsv5620825insertion1nstd207human GRCh38 chr3: 194,421,153-194,421,153 , GRCh37.p13 chr3: 194,141,882-194,141,882 ATP13A3
    nsv5618812insertion1nstd207human GRCh38 chr3: 194,421,139-194,421,139 , GRCh37.p13 chr3: 194,141,868-194,141,868 ATP13A3
    nsv5608642insertion1nstd207human GRCh38 chr3: 194,421,137-194,421,137 , GRCh37.p13 chr3: 194,141,866-194,141,866 ATP13A3
    nsv5583704copy number variation1nstd207human GRCh38 chr3: 194,400,435-194,401,191 , GRCh37.p13 chr3: 194,121,164-194,121,920 ATP13A3
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5450429copy number variation1nstd206human GRCh38 chr3: 194,400,443-194,401,192 , GRCh37.p13 chr3: 194,121,172-194,121,921 ATP13A3
    nsv5449508copy number variation1nstd206human GRCh38 chr3: 194,433,000-194,791,574 , GRCh37.p13 chr3: 194,153,729-194,512,303 RNU6-1101P, FAM151AP1, 11 more genes
    nsv5413699mobile element insertion1nstd206human GRCh38 chr3: 194,440,857-194,440,908 , GRCh37.p13 chr3: 194,161,586-194,161,637 ATP13A3
    nsv5393907mobile element deletion2nstd186human GRCh37 chr3: 194,121,172-194,121,921 , GRCh38.p12 chr3: 194,400,443-194,401,192 ATP13A3
    nsv5352377translocation1nstd200human GRCh38 chr3: 194,473,728-194,473,728 , GRCh38 chr3: 194,473,436-194,473,436 , GRCh37.p13 chr3: 194,194,165-194,194,165 , GRCh37.p13 chr3: 194,194,457-194,194,457 ATP13A3
    nsv5329204mobile element deletion1nstd204human GRCh38.p13 chr3: 194,400,443-194,401,192 , GRCh37.p13 chr3: 194,121,172-194,121,921 ATP13A3
    nsv5034831mobile element deletion1nstd200human GRCh38 chr3: 194,400,443-194,401,192 , GRCh37.p13 chr3: 194,121,172-194,121,921 ATP13A3
    nsv4928328copy number variation1nstd200human GRCh38 chr3: 194,432,011-194,432,849 , GRCh37.p13 chr3: 194,152,740-194,153,578 ATP13A3
    nsv4928327copy number variation1nstd200human GRCh38 chr3: 194,416,922-194,418,703 , GRCh37.p13 chr3: 194,137,651-194,139,432 ATP13A3
    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