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 369

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7072028inversion1nstd229human GRCh38 chr10: 62,261,311-62,267,028 , GRCh37.p13 chr10: 64,021,070-64,026,787 RTKN2
    nsv6896117copy number variation1nstd229human GRCh38 chr10: 62,268,064-62,278,335 , GRCh37.p13 chr10: 64,027,823-64,038,094 RTKN2
    nsv6895892copy number variation1nstd229human GRCh38 chr10: 62,211,501-62,217,900 , GRCh37.p13 chr10: 63,971,260-63,977,659 RTKN2
    nsv6892438copy number variation1nstd229human GRCh38 chr10: 62,229,176-62,287,652 , GRCh37.p13 chr10: 63,988,935-64,047,411 LINC02621, RTKN2
    nsv6892039copy number variation1nstd229human GRCh38 chr10: 62,138,002-62,261,592 , GRCh37.p13 chr10: 63,897,761-64,021,351 RTKN2
    nsv6891943copy number variation1nstd229human GRCh38 chr10: 62,175,083-62,175,173 , GRCh37.p13 chr10: 63,934,842-63,934,932 RTKN2
    nsv6890238copy number variation1nstd229human GRCh38 chr10: 62,215,301-62,228,800 , GRCh37.p13 chr10: 63,975,060-63,988,559 RTKN2
    nsv6884675copy number variation1nstd229human GRCh38 chr10: 62,175,576-62,183,424 , GRCh37.p13 chr10: 63,935,335-63,943,183 RTKN2
    nsv6883240copy number variation1nstd229human GRCh38 chr10: 62,167,876-62,167,992 , GRCh37.p13 chr10: 63,927,635-63,927,751 RTKN2
    nsv6882920copy number variation1nstd229human GRCh38 chr10: 62,194,028-62,194,441 , GRCh37.p13 chr10: 63,953,787-63,954,200 RTKN2
    nsv6879680copy number variation1nstd229human GRCh38 chr10: 62,193,526-62,197,052 , GRCh37.p13 chr10: 63,953,285-63,956,811 RTKN2
    nsv6637363copy number variation1nstd102humanUncertain significance GRCh37 chr10: 57,941,252-64,846,332 , GRCh38.p12 chr10: 56,181,491-63,086,572 TMEM26-AS1, LOC112268068, 53 more genes
    nsv6591910inversion1nstd223human GRCh38 chr10: 62,202,814-62,203,543 , GRCh37.p13 chr10: 63,962,573-63,963,302 RTKN2
    nsv6591150inversion1nstd223human GRCh38 chr10: 62,254,666-62,256,368 , GRCh37.p13 chr10: 64,014,425-64,016,127 RTKN2
    nsv6584735inversion1nstd223human GRCh38 chr10: 62,211,643-62,212,556 , GRCh37.p13 chr10: 63,971,402-63,972,315 RTKN2
    nsv6584438inversion1nstd223human GRCh38 chr10: 62,242,123-62,242,450 , GRCh37.p13 chr10: 64,001,882-64,002,209 RTKN2
    nsv6580716inversion1nstd223human GRCh38 chr10: 62,174,305-62,174,565 , GRCh37.p13 chr10: 63,934,064-63,934,324 RTKN2
    nsv6452910copy number variation1nstd223human GRCh38 chr10: 62,251,501-62,253,000 , GRCh37.p13 chr10: 64,011,260-64,012,759 RTKN2
    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