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 203

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880981copy number variation1nstd209human GRCh38 chr2: 9,406,008-9,406,507 , GRCh37.p13 chr2: 9,546,137-9,546,636 ASAP2, ITGB1BP1
    nsv5624241insertion1nstd207human GRCh38 chr2: 9,406,255-9,406,255 , GRCh37.p13 chr2: 9,546,384-9,546,384 ITGB1BP1
    nsv5623210insertion3nstd207human GRCh38 chr2: 9,406,510-9,406,510 , GRCh37.p13 chr2: 9,546,639-9,546,639 ITGB1BP1
    nsv5621739insertion1nstd207human GRCh38 chr2: 9,406,284-9,406,284 , GRCh37.p13 chr2: 9,546,413-9,546,413 ITGB1BP1
    nsv5613769insertion3nstd207human GRCh38 chr2: 9,406,031-9,406,031 , GRCh37.p13 chr2: 9,546,160-9,546,160 ITGB1BP1, ASAP2
    nsv5609862insertion1nstd207human GRCh38 chr2: 9,406,143-9,406,143 , GRCh37.p13 chr2: 9,546,272-9,546,272 ITGB1BP1, ASAP2
    nsv5605190insertion1nstd207human GRCh38 chr2: 9,406,228-9,406,228 , GRCh37.p13 chr2: 9,546,357-9,546,357 ITGB1BP1
    nsv5582369copy number variation1nstd207human GRCh38 chr2: 9,406,363-9,406,422 , GRCh37.p13 chr2: 9,546,492-9,546,551 ITGB1BP1
    nsv5575758copy number variation1nstd207human GRCh38 chr2: 9,406,031-9,406,198 , GRCh37.p13 chr2: 9,546,160-9,546,327 ASAP2, ITGB1BP1
    nsv5567276copy number variation1nstd207human GRCh38 chr2: 9,406,008-9,406,059 , GRCh37.p13 chr2: 9,546,137-9,546,188 ITGB1BP1, ASAP2
    nsv5566853copy number variation1nstd207human GRCh38 chr2: 9,406,172-9,406,507 , GRCh37.p13 chr2: 9,546,301-9,546,636 ASAP2, ITGB1BP1
    nsv5383151copy number variation1nstd186human GRCh37 chr2: 9,546,290-9,546,561 , GRCh38.p12 chr2: 9,406,161-9,406,432 ASAP2, ITGB1BP1
    nsv4770138copy number variation1nstd200human GRCh37 chr2: 9,546,290-9,546,561 , GRCh38.p12 chr2: 9,406,161-9,406,432 ASAP2, ITGB1BP1
    nsv4741702copy number variation1nstd199human GRCh37 chr2: 9,546,170-9,546,224 , GRCh38.p12 chr2: 9,406,041-9,406,095 ITGB1BP1, ASAP2
    nsv4595871copy number variation1nstd183human GRCh37 chr2: 9,563,268-9,563,560 , GRCh38.p12 chr2: 9,423,139-9,423,431 CPSF3, ITGB1BP1
    nsv4586774copy number variation2nstd183human GRCh37 chr2: 9,546,103-9,546,775 , GRCh38.p12 chr2: 9,405,974-9,406,646 ITGB1BP1, ASAP2
    nsv4408884copy number variation1nstd174human GRCh37 chr2: 9,546,353-9,546,736 , GRCh38.p12 chr2: 9,406,224-9,406,607 ITGB1BP1
    nsv4407608copy number variation1nstd174human GRCh37 chr2: 9,546,094-9,546,805 , GRCh38.p12 chr2: 9,405,965-9,406,676 ITGB1BP1, ASAP2
    nsv4396474copy number variation1nstd174human GRCh37 chr2: 9,546,030-9,546,805 , GRCh38.p12 chr2: 9,405,901-9,406,676 ASAP2, ITGB1BP1
    nsv4057234copy number variation1nstd166human GRCh37.p13 chr2: 9,546,180-9,546,630 , GRCh38.p12 chr2: 9,406,051-9,406,501 ASAP2, ITGB1BP1
    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