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 335

    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
    nsv7071055inversion1nstd229human GRCh38 chr10: 31,716,519-31,893,416 , GRCh37.p13 chr10: 32,005,447-32,182,344 ARHGAP12
    nsv7069906inversion1nstd229human GRCh38 chr10: 31,716,506-31,893,425 , GRCh37.p13 chr10: 32,005,434-32,182,353 ARHGAP12
    nsv6895406copy number variation1nstd229human GRCh38 chr10: 31,865,130-31,868,134 , GRCh37.p13 chr10: 32,154,058-32,157,062 ARHGAP12
    nsv6894751copy number variation1nstd229human GRCh38 chr10: 31,821,815-31,822,013 , GRCh37.p13 chr10: 32,110,743-32,110,941 ARHGAP12
    nsv6894377copy number variation1nstd229human GRCh38 chr10: 28,466,728-36,061,502 , GRCh37.p13 chr10: 28,755,657-36,350,430 LOC105376482, LOC101929431, 130 more genes
    nsv6892919copy number variation1nstd229human GRCh38 chr10: 31,921,185-31,952,672 , GRCh37.p13 chr10: 32,210,113-32,241,600 ARHGAP12, LOC107984219
    nsv6892407copy number variation1nstd229human GRCh38 chr10: 31,846,103-31,853,547 , GRCh37.p13 chr10: 32,135,031-32,142,475 ARHGAP12
    nsv6884550copy number variation1nstd229human GRCh38 chr10: 31,911,105-31,935,055 , GRCh37.p13 chr10: 32,200,033-32,223,983 ARHGAP12, HMGB1P7, 1 more genes
    nsv6883414copy number variation1nstd229human GRCh38 chr10: 31,845,756-31,854,403 , GRCh37.p13 chr10: 32,134,684-32,143,331 ARHGAP12
    nsv6882759copy number variation1nstd229human GRCh38 chr10: 31,892,801-31,895,500 , GRCh37.p13 chr10: 32,181,729-32,184,428 ARHGAP12
    nsv6879391copy number variation1nstd229human GRCh38 chr10: 31,925,301-31,951,800 , GRCh37.p13 chr10: 32,214,229-32,240,728 LOC107984219, ARHGAP12
    nsv6879073copy number variation1nstd229human GRCh38 chr10: 31,832,409-31,832,950 , GRCh37.p13 chr10: 32,121,337-32,121,878 ARHGAP12
    nsv6592743inversion1nstd223human GRCh38 chr10: 31,916,769-31,917,257 , GRCh37.p13 chr10: 32,205,697-32,206,185 ARHGAP12
    nsv6582027inversion1nstd223human GRCh38 chr10: 26,903,422-36,846,484 , GRCh37.p13 chr10: 27,192,351-37,135,412 KIF5B, EPC1-AS1, 167 more genes
    nsv6576879inversion1nstd223human GRCh38 chr10: 31,815,471-31,816,503 , GRCh37.p13 chr10: 32,104,399-32,105,431 ARHGAP12
    nsv6449440copy number variation1nstd223human GRCh38 chr10: 31,879,185-31,880,058 , GRCh37.p13 chr10: 32,168,113-32,168,986 ARHGAP12
    nsv6445458copy number variation1nstd223human GRCh38 chr10: 31,909,734-31,912,483 , GRCh37.p13 chr10: 32,198,662-32,201,411 ARHGAP12, HMGB1P7
    nsv6440865copy number variation1nstd223human GRCh38 chr10: 31,885,673-31,978,421 , GRCh37.p13 chr10: 32,174,601-32,267,349 HMGB1P7, LOC107984219, 1 more genes
    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