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 587

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137806copy number variation1nstd102humanUncertain significance GRCh37 chr3: 196,539,700-196,612,739 , GRCh38.p12 chr3: 196,812,829-196,885,868 SENP5, PAK2
    nsv5980449copy number variation1nstd102humanrisk factor GRCh37 chr3: 195,693,872-197,376,871 , GRCh38.p12 chr3: 195,967,001-197,650,000 RN7SL434P, RNU6-1279P, 54 more genes
    nsv5964116insertion1nstd209human GRCh38 chr3: 196,751,691-196,751,691 , GRCh37.p13 chr3: 196,478,562-196,478,562 PAK2
    nsv5902557copy number variation1nstd209human GRCh38 chr3: 196,809,206-196,809,415 , GRCh37.p13 chr3: 196,536,077-196,536,286 PAK2
    nsv5900564copy number variation1nstd209human GRCh38 chr3: 196,825,165-196,826,739 , GRCh37.p13 chr3: 196,552,036-196,553,610 PAK2
    nsv5894513copy number variation1nstd209human GRCh38 chr3: 196,767,671-196,775,557 , GRCh37.p13 chr3: 196,494,542-196,502,428 PAK2
    nsv5894304copy number variation1nstd209human GRCh38 chr3: 196,825,226-196,825,522 , GRCh37.p13 chr3: 196,552,097-196,552,393 PAK2
    nsv5888019copy number variation1nstd209human GRCh38 chr3: 196,767,512-196,771,582 , GRCh37.p13 chr3: 196,494,383-196,498,453 PAK2
    nsv5835750copy number variation1nstd209human GRCh38 chr3: 196,825,305-196,826,866 , GRCh37.p13 chr3: 196,552,176-196,553,737 PAK2
    nsv5835522copy number variation1nstd209human GRCh38 chr3: 196,767,690-196,772,121 , GRCh37.p13 chr3: 196,494,561-196,498,992 PAK2
    nsv5835200copy number variation1nstd209human GRCh38 chr3: 196,768,615-196,775,485 , GRCh37.p13 chr3: 196,495,486-196,502,356 PAK2
    nsv5689242mobile element insertion1nstd211human GRCh38 chr3: 196,746,830-196,746,830 , GRCh37.p13 chr3: 196,473,701-196,473,701 RNU4-89P, PAK2
    nsv5683639mobile element insertion1nstd211human GRCh38 chr3: 196,822,172-196,822,172 , GRCh37.p13 chr3: 196,549,043-196,549,043 PAK2
    nsv5622990insertion1nstd207human GRCh38 chr3: 196,811,226-196,811,226 , GRCh37.p13 chr3: 196,538,097-196,538,097 PAK2
    nsv5616537insertion1nstd207human GRCh38 chr3: 196,811,273-196,811,273 , GRCh37.p13 chr3: 196,538,144-196,538,144 PAK2
    nsv5615646insertion1nstd207human GRCh38 chr3: 196,811,324-196,811,324 , GRCh37.p13 chr3: 196,538,195-196,538,195 PAK2
    nsv5614674insertion1nstd207human GRCh38 chr3: 196,811,003-196,811,003 , GRCh37.p13 chr3: 196,537,874-196,537,874 PAK2
    nsv5609018insertion1nstd207human GRCh38 chr3: 196,811,213-196,811,213 , GRCh37.p13 chr3: 196,538,084-196,538,084 PAK2
    nsv5608424insertion1nstd207human GRCh38 chr3: 196,811,221-196,811,221 , GRCh37.p13 chr3: 196,538,092-196,538,092 PAK2
    nsv5582195copy number variation1nstd207human GRCh38 chr3: 196,811,008-196,811,188 , GRCh37.p13 chr3: 196,537,879-196,538,059 PAK2
    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