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 502

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130323insertion1nstd186human GRCh37 chr22: 43,367,894-43,367,930 , GRCh38.p12 chr22: 42,971,888-42,971,924 PACSIN2
    nsv6129863insertion1nstd186human GRCh37 chr22: 43,346,427-43,346,431 , GRCh38.p12 chr22: 42,950,421-42,950,425 PACSIN2
    nsv5979189insertion1nstd209human GRCh38 chr22: 42,971,873-42,971,873 , GRCh37.p13 chr22: 43,367,879-43,367,879 PACSIN2
    nsv5968021insertion1nstd209human GRCh38 chr22: 42,987,493-42,987,493 , GRCh37.p13 chr22: 43,383,499-43,383,499 PACSIN2
    nsv5964203copy number variation1nstd209human GRCh38 chr22: 42,925,207-42,925,416 , GRCh37.p13 chr22: 43,321,213-43,321,422 PACSIN2
    nsv5962317copy number variation1nstd209human GRCh38 chr22: 42,896,342-42,896,399 , GRCh37.p13 chr22: 43,292,348-43,292,405 , PACSIN2
    nsv5958396copy number variation1nstd209human GRCh38 chr22: 42,929,945-42,930,004 , GRCh37.p13 chr22: 43,325,951-43,326,010 PACSIN2
    nsv5955359copy number variation1nstd209human GRCh38 chr22: 42,984,117-42,987,677 , GRCh37.p13 chr22: 43,380,123-43,383,683 PACSIN2
    nsv5953740copy number variation1nstd209human GRCh38 chr22: 42,878,858-42,878,910 , GRCh37.p13 chr22: 43,274,864-43,274,916 PACSIN2
    nsv5952825copy number variation1nstd209human GRCh38 chr22: 42,901,647-42,901,901 , GRCh37.p13 chr22: 43,297,653-43,297,907 PACSIN2
    nsv5887006copy number variation2nstd209human GRCh38 chr22: 42,985,213-42,987,196 , GRCh37.p13 chr22: 43,381,219-43,383,202 PACSIN2
    nsv5877722copy number variation1nstd209human GRCh38 chr22: 42,986,464-42,987,740 , GRCh37.p13 chr22: 43,382,470-43,383,746 PACSIN2
    nsv5877442copy number variation1nstd209human GRCh38 chr22: 42,983,963-42,987,690 , GRCh37.p13 chr22: 43,379,969-43,383,696 PACSIN2
    nsv5716258mobile element insertion2nstd211human GRCh38 chr22: 42,988,174-42,988,174 , GRCh37.p13 chr22: 43,384,180-43,384,180 PACSIN2
    nsv5673276copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,440,000-43,780,000 , GRCh38.p12 chr22: 42,043,996-43,383,994 RPL5P34, ARFGAP3, 48 more genes
    nsv5672488insertion1nstd207human GRCh38 chr22: 42,878,858-42,878,858 , GRCh37.p13 chr22: 43,274,864-43,274,864 PACSIN2
    nsv5672084insertion1nstd207human GRCh38 chr22: 42,971,873-42,971,873 , GRCh37.p13 chr22: 43,367,879-43,367,879 PACSIN2
    nsv5666773insertion1nstd207human GRCh38 chr22: 42,950,410-42,950,410 , GRCh37.p13 chr22: 43,346,416-43,346,416 PACSIN2
    nsv5664878insertion1nstd207human GRCh38 chr22: 42,981,488-42,981,488 , GRCh37.p13 chr22: 43,377,494-43,377,494 PACSIN2
    nsv5599839copy number variation1nstd207human GRCh38 chr22: 42,896,342-42,896,399 , GRCh37.p13 chr22: 43,292,348-43,292,405 , PACSIN2
    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