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 1685

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960762insertion1nstd209human GRCh38 chr8: 103,706,759-103,706,759 , GRCh37.p13 chr8: 104,718,987-104,718,987 RIMS2
    nsv5960200insertion1nstd209human GRCh38 chr8: 104,138,576-104,138,576 , GRCh37.p13 chr8: 105,150,804-105,150,804 RIMS2
    nsv5959653insertion1nstd209human GRCh38 chr8: 103,840,433-103,840,433 , GRCh37.p13 chr8: 104,852,661-104,852,661 RIMS2
    nsv5957494insertion1nstd209human GRCh38 chr8: 103,978,360-103,978,360 , GRCh37.p13 chr8: 104,990,588-104,990,588 LOC105375689, RIMS2
    nsv5950543insertion1nstd209human GRCh38 chr8: 103,559,056-103,559,056 , GRCh37.p13 chr8: 104,571,284-104,571,284 PTMAP15, RIMS2
    nsv5923516copy number variation1nstd209human GRCh38 chr8: 103,852,268-103,852,393 , GRCh37.p13 chr8: 104,864,496-104,864,621 RIMS2
    nsv5921965copy number variation1nstd209human GRCh38 chr8: 103,854,817-103,854,949 , GRCh37.p13 chr8: 104,867,045-104,867,177 RIMS2
    nsv5921305copy number variation1nstd209human GRCh38 chr8: 103,506,435-103,506,506 , GRCh37.p13 chr8: 104,518,663-104,518,734 RIMS2
    nsv5920176copy number variation1nstd209human GRCh38 chr8: 103,695,773-103,708,954 , GRCh37.p13 chr8: 104,708,001-104,721,182 RIMS2
    nsv5919890copy number variation1nstd209human GRCh38 chr8: 103,927,392-103,928,864 , GRCh37.p13 chr8: 104,939,620-104,941,092 RIMS2
    nsv5919507copy number variation1nstd209human GRCh38 chr8: 104,101,037-104,101,103 , GRCh37.p13 chr8: 105,113,265-105,113,331 LOC105375688, RIMS2
    nsv5919478copy number variation1nstd209human GRCh38 chr8: 103,828,669-103,829,507 , GRCh37.p13 chr8: 104,840,897-104,841,735 RIMS2
    nsv5917403copy number variation1nstd209human GRCh38 chr8: 103,939,416-103,942,204 , GRCh37.p13 chr8: 104,951,644-104,954,432 RIMS2
    nsv5916234copy number variation1nstd209human GRCh38 chr8: 103,546,307-103,574,496 , GRCh37.p13 chr8: 104,558,535-104,586,724 RIMS2, LOC101101841, 1 more genes
    nsv5915282copy number variation1nstd209human GRCh38 chr8: 103,894,153-103,900,468 , GRCh37.p13 chr8: 104,906,381-104,912,696 RIMS2
    nsv5912585copy number variation1nstd209human GRCh38 chr8: 104,255,192-104,255,292 , GRCh37.p13 chr8: 105,267,420-105,267,520 RIMS2
    nsv5911926copy number variation1nstd209human GRCh38 chr8: 103,746,255-103,751,921 , GRCh37.p13 chr8: 104,758,483-104,764,149 RIMS2
    nsv5911522copy number variation1nstd209human GRCh38 chr8: 103,933,277-103,933,350 , GRCh37.p13 chr8: 104,945,505-104,945,578 RIMS2
    nsv5862173copy number variation1nstd209human GRCh38 chr8: 103,546,295-103,559,027 , GRCh37.p13 chr8: 104,558,523-104,571,255 RIMS2, PTMAP15
    nsv5857873copy number variation1nstd209human GRCh38 chr8: 103,746,210-103,751,441 , GRCh37.p13 chr8: 104,758,438-104,763,669 RIMS2
    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