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 427

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972734inversion1nstd209human GRCh38 chr2: 107,351,674-107,352,512 , GRCh37.p13 chr2: 107,968,130-107,968,968 LINC01789
    nsv5953334insertion1nstd209human GRCh38 chr2: 107,308,151-107,308,151 , GRCh37.p13 chr2: 107,924,607-107,924,607 LINC01789
    nsv5883146copy number variation1nstd209human GRCh38 chr2: 107,342,494-107,346,186 , GRCh37.p13 chr2: 107,958,950-107,962,642 LINC01789
    nsv5876276copy number variation1nstd209human GRCh38 chr2: 107,310,342-107,311,431 , GRCh37.p13 chr2: 107,926,798-107,927,887 LINC01789
    nsv5871446copy number variation1nstd209human GRCh38 chr2: 107,309,925-107,310,265 , GRCh37.p13 chr2: 107,926,381-107,926,721 LINC01789
    nsv5871037copy number variation1nstd209human GRCh38 chr2: 107,282,727-107,287,364 , GRCh37.p13 chr2: 107,899,183-107,903,820 LINC01789
    nsv5868662copy number variation1nstd209human GRCh38 chr2: 106,240,685-107,908,171 , GRCh37.p13 chr2: 106,857,141-108,524,627 , LOC105373539, 21 more genes
    nsv5831077copy number variation1nstd209human GRCh38 chr2: 107,340,987-107,342,474 , GRCh37.p13 chr2: 107,957,443-107,958,930 LINC01789
    nsv5831076copy number variation1nstd209human GRCh38 chr2: 107,282,711-107,287,267 , GRCh37.p13 chr2: 107,899,167-107,903,723 LINC01789
    nsv5689771mobile element insertion1nstd211human GRCh38 chr2: 107,268,821-107,268,821 , GRCh37.p13 chr2: 107,885,277-107,885,277 LINC01789
    nsv5676713mobile element insertion2nstd211human GRCh38 chr2: 107,308,168-107,308,168 , GRCh37.p13 chr2: 107,924,624-107,924,624 LINC01789
    nsv5610500insertion1nstd207human GRCh38 chr2: 107,308,151-107,308,151 , GRCh37.p13 chr2: 107,924,607-107,924,607 LINC01789
    nsv5568658copy number variation1nstd207human GRCh38 chr2: 107,309,925-107,310,265 , GRCh37.p13 chr2: 107,926,381-107,926,721 LINC01789
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5539511insertion1nstd206human GRCh38 chr2: 107,308,151-107,308,151 , GRCh37.p13 chr2: 107,924,607-107,924,607 LINC01789
    nsv5453397copy number variation1nstd206human GRCh38 chr2: 107,260,421-107,261,246 , GRCh37.p13 chr2: 107,876,877-107,877,702 LINC01789
    nsv5452425copy number variation1nstd206human GRCh38 chr2: 106,078,600-107,921,618 , GRCh37.p13 chr2: 106,695,056-108,538,074 , RPS21P2, 26 more genes
    nsv5439457copy number variation1nstd206human GRCh38 chr2: 106,209,999-107,914,000 , GRCh37.p13 chr2: 106,826,455-108,530,456 , PPP1R2P5, 22 more genes
    nsv5436158copy number variation1nstd206human GRCh38 chr2: 107,282,728-107,287,365 , GRCh37.p13 chr2: 107,899,184-107,903,821 LINC01789
    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