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 258

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113061copy number variation1nstd186human GRCh37 chrX: 24,756,048-24,756,359 , GRCh38.p12 chrX: 24,737,931-24,738,242 POLA1
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5952397insertion1nstd209human GRCh38 chrX: 24,824,700-24,824,700 , GRCh37.p13 chrX: 24,842,817-24,842,817 POLA1
    nsv5951933insertion1nstd209human GRCh38 chrX: 24,757,436-24,757,436 , GRCh37.p13 chrX: 24,775,553-24,775,553 POLA1
    nsv5883293copy number variation1nstd209human GRCh38 chrX: 24,958,174-24,958,235 , GRCh37.p13 chrX: 24,976,291-24,976,352 POLA1
    nsv5878491copy number variation1nstd209human GRCh38 chrX: 24,737,912-24,738,241 , GRCh37.p13 chrX: 24,756,029-24,756,358 POLA1
    nsv5875206copy number variation1nstd209human GRCh38 chrX: 24,972,218-24,975,269 , GRCh37.p13 chrX: 24,990,335-24,993,386 POLA1
    nsv5870025copy number variation1nstd209human GRCh38 chrX: 24,932,007-24,932,141 , GRCh37.p13 chrX: 24,950,124-24,950,258 POLA1
    nsv5729724mobile element insertion1nstd211human GRCh38 chrX: 24,712,610-24,712,610 , GRCh37.p13 chrX: 24,730,727-24,730,727 POLA1
    nsv5722416mobile element insertion1nstd211human GRCh38 chrX: 24,752,794-24,752,794 , GRCh37.p13 chrX: 24,770,911-24,770,911 POLA1
    nsv5716240mobile element insertion2nstd211human GRCh38 chrX: 24,824,716-24,824,716 , GRCh37.p13 chrX: 24,842,833-24,842,833 POLA1
    nsv5668554copy number variation1nstd207human GRCh38 chrX: 24,737,912-24,738,241 , GRCh37.p13 chrX: 24,756,029-24,756,358 POLA1
    nsv5613478insertion1nstd207human GRCh38 chrX: 24,709,091-24,709,091 , GRCh37.p13 chrX: 24,727,208-24,727,208 POLA1
    nsv5564483copy number variation1nstd102humanUncertain significance GRCh37 chrX: 24,712,079-24,839,720 , GRCh38.p12 chrX: 24,693,962-24,821,603 EEF1B2P3, SCARNA23, 1 more genes
    nsv5562559mobile element insertion1nstd206human GRCh38 chrX: 24,824,716-24,824,767 , GRCh37.p13 chrX: 24,842,833-24,842,884 POLA1
    nsv5433915copy number variation1nstd206human GRCh38 chrX: 24,958,174-24,958,237 , GRCh37.p13 chrX: 24,976,291-24,976,354 POLA1
    nsv5433731copy number variation1nstd206human GRCh38 chrX: 24,972,261-24,975,207 , GRCh37.p13 chrX: 24,990,378-24,993,324 POLA1
    nsv5432765copy number variation1nstd206human GRCh38 chrX: 24,995,849-24,999,810 , GRCh37.p13 chrX: 25,013,966-25,017,927 POLA1
    nsv5431985copy number variation1nstd206human GRCh38 chrX: 24,737,931-24,738,242 , GRCh37.p13 chrX: 24,756,048-24,756,359 POLA1
    nsv5430454copy number variation1nstd206human GRCh38 chrX: 24,770,491-24,778,864 , GRCh37.p13 chrX: 24,788,608-24,796,981 POLA1
    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