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 591

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964782insertion1nstd209human GRCh38 chr3: 138,705,180-138,705,180 , GRCh37.p13 chr3: 138,424,022-138,424,022 PIK3CB
    nsv5903148copy number variation1nstd209human GRCh38 chr3: 138,831,328-138,831,661 , GRCh37.p13 chr3: 138,550,170-138,550,503 PIK3CB
    nsv5897907copy number variation1nstd209human GRCh38 chr3: 138,826,402-138,826,461 , GRCh37.p13 chr3: 138,545,244-138,545,303 PIK3CB, EEF1A1P25
    nsv5896356copy number variation1nstd209human GRCh38 chr3: 138,771,840-138,771,900 , GRCh37.p13 chr3: 138,490,682-138,490,742 PIK3CB
    nsv5889866copy number variation1nstd209human GRCh38 chr3: 137,097,814-139,588,879 , GRCh37.p13 chr3: 136,816,656-139,307,721 , LOC105374127, 42 more genes
    nsv5834334copy number variation1nstd209human GRCh38 chr3: 138,769,034-138,770,033 , GRCh37.p13 chr3: 138,487,876-138,488,875 PIK3CB
    nsv5834333copy number variation1nstd209human GRCh38 chr3: 138,732,057-138,734,295 , GRCh37.p13 chr3: 138,450,899-138,453,137 PIK3CB
    nsv5693015mobile element insertion2nstd211human GRCh38 chr3: 138,684,987-138,684,987 , GRCh37.p13 chr3: 138,403,829-138,403,829 PIK3CB
    nsv5680862mobile element insertion2nstd211human GRCh38 chr3: 138,725,217-138,725,217 , GRCh37.p13 chr3: 138,444,059-138,444,059 PIK3CB
    nsv5614470insertion1nstd207human GRCh38 chr3: 138,768,205-138,768,205 , GRCh37.p13 chr3: 138,487,047-138,487,047 PIK3CB
    nsv5452445copy number variation1nstd206human GRCh38 chr3: 138,810,730-138,815,039 , GRCh37.p13 chr3: 138,529,572-138,533,881 PIK3CB
    nsv5452102copy number variation1nstd206human GRCh38 chr3: 138,766,529-138,767,351 , GRCh37.p13 chr3: 138,485,371-138,486,193 PIK3CB
    nsv5450056copy number variation1nstd206human GRCh38 chr3: 138,692,909-138,693,474 , GRCh37.p13 chr3: 138,411,751-138,412,316 PIK3CB
    nsv5449832copy number variation1nstd206human GRCh38 chr3: 138,832,806-138,832,993 , GRCh37.p13 chr3: 138,551,648-138,551,835 PIK3CB
    nsv5447963copy number variation1nstd206human GRCh38 chr3: 138,709,745-138,709,836 , GRCh37.p13 chr3: 138,428,587-138,428,678 PIK3CB
    nsv5446133copy number variation1nstd206human GRCh38 chr3: 138,789,950-138,794,640 , GRCh37.p13 chr3: 138,508,792-138,513,482 PIK3CB
    nsv5446007copy number variation1nstd206human GRCh38 chr3: 138,789,399-138,790,784 , GRCh37.p13 chr3: 138,508,241-138,509,626 PIK3CB
    nsv5443886copy number variation1nstd206human GRCh38 chr3: 138,480,477-138,945,708 , GRCh37.p13 chr3: 138,199,319-138,664,550 ESYT3, GAPDHP39, 10 more genes
    nsv5442407copy number variation1nstd206human GRCh38 chr3: 138,788,114-138,788,178 , GRCh37.p13 chr3: 138,506,956-138,507,020 PIK3CB
    nsv5440238copy number variation1nstd206human GRCh38 chr3: 138,805,859-138,806,010 , GRCh37.p13 chr3: 138,524,701-138,524,852 PIK3CB
    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