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 603

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7062430inversion1nstd229human GRCh38 chr22: 30,713,704-30,713,749 , GRCh37.p13 chr22: 31,109,691-31,109,736 OSBP2
    nsv7061896inversion1nstd229human GRCh38 chr22: 30,780,746-30,787,412 , GRCh37.p13 chr22: 31,176,733-31,183,399 OSBP2
    nsv7036315copy number variation1nstd229human GRCh38 chr22: 30,773,364-30,783,466 , GRCh37.p13 chr22: 31,169,351-31,179,453 OSBP2
    nsv7035858copy number variation1nstd229human GRCh38 chr22: 30,895,677-30,900,044 , GRCh37.p13 chr22: 31,291,664-31,296,031 LOC107985544, OSBP2
    nsv7035800copy number variation1nstd229human GRCh38 chr22: 30,480,363-30,697,469 , GRCh37.p13 chr22: 30,876,350-31,093,456 SIRPAP1, DUSP18, 10 more genes
    nsv7034702copy number variation1nstd229human GRCh38 chr22: 30,814,044-30,856,630 , GRCh37.p13 chr22: 31,210,031-31,252,617 OSBP2
    nsv7034089copy number variation1nstd229human GRCh38 chr22: 30,803,895-30,826,537 , GRCh37.p13 chr22: 31,199,882-31,222,524 OSBP2
    nsv7032401copy number variation1nstd229human GRCh38 chr22: 30,908,205-30,915,891 , GRCh37.p13 chr22: 31,304,192-31,311,878 LOC107985544, OSBP2
    nsv7032215copy number variation1nstd229human GRCh38 chr22: 30,688,538-30,725,927 , GRCh37.p13 chr22: 31,084,525-31,121,914 OSBP2
    nsv7031798copy number variation1nstd229human GRCh38 chr22: 30,805,765-30,814,798 , GRCh37.p13 chr22: 31,201,752-31,210,785 OSBP2
    nsv7030958copy number variation1nstd229human GRCh38 chr22: 30,741,801-30,741,943 , GRCh37.p13 chr22: 31,137,788-31,137,930 OSBP2
    nsv7030509copy number variation1nstd229human GRCh38 chr22: 30,843,071-30,858,364 , GRCh37.p13 chr22: 31,239,058-31,254,351 OSBP2
    nsv7029977copy number variation1nstd229human GRCh38 chr22: 30,745,378-30,750,900 , GRCh37.p13 chr22: 31,141,365-31,146,887 OSBP2
    nsv7029843copy number variation1nstd229human GRCh38 chr22: 30,703,116-30,729,158 , GRCh37.p13 chr22: 31,099,103-31,125,145 OSBP2
    nsv7029788copy number variation1nstd229human GRCh38 chr22: 30,691,771-30,691,944 , GRCh37.p13 chr22: 31,087,758-31,087,931 OSBP2
    nsv7028739copy number variation1nstd229human GRCh38 chr22: 30,702,701-30,721,300 , GRCh37.p13 chr22: 31,098,688-31,117,287 OSBP2
    nsv7027285copy number variation1nstd229human GRCh38 chr22: 30,698,783-30,706,797 , GRCh37.p13 chr22: 31,094,770-31,102,784 OSBP2
    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