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 342

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077847inversion1nstd229human GRCh38 chr13: 62,019,069-62,027,115 , GRCh37.p13 chr13: 62,593,202-62,601,248 LINC00358
    nsv7071638inversion1nstd229human GRCh38 chr13: 55,583,879-63,209,085 , GRCh37.p13 chr13: 56,158,014-63,783,218 MIR3169, PCDH20, 66 more genes
    nsv7067544inversion1nstd229human GRCh38 chr13: 62,015,676-62,027,112 , GRCh37.p13 chr13: 62,589,809-62,601,245 LINC00358
    nsv7063310inversion1nstd229human GRCh38 chr13: 60,352,407-63,352,731 , GRCh37.p13 chr13: 60,926,541-63,926,864 TDRD3, LOC105370230, 23 more genes
    nsv6956288copy number variation1nstd229human GRCh38 chr13: 62,020,801-62,022,928 , GRCh37.p13 chr13: 62,594,934-62,597,061 LINC00358
    nsv6953120copy number variation1nstd229human GRCh38 chr13: 61,944,212-62,108,496 , GRCh37.p13 chr13: 62,518,345-62,682,629 LINC00358
    nsv6952716copy number variation1nstd229human GRCh38 chr13: 61,349,430-62,117,406 , GRCh37.p13 chr13: 61,923,563-62,691,539 LINC02339, PCDH20, 3 more genes
    nsv6947621copy number variation1nstd229human GRCh38 chr13: 62,003,094-62,071,027 , GRCh37.p13 chr13: 62,577,227-62,645,160 LINC00358
    nsv6946472copy number variation1nstd229human GRCh38 chr13: 62,026,207-62,035,724 , GRCh37.p13 chr13: 62,600,340-62,609,857 LINC00358
    nsv6945849copy number variation1nstd229human GRCh38 chr13: 61,945,598-62,011,210 , GRCh37.p13 chr13: 62,519,731-62,585,343 LINC00358
    nsv6944737copy number variation1nstd229human GRCh38 chr13: 61,676,666-62,422,606 , GRCh37.p13 chr13: 62,250,799-62,996,739 LINC01074, RPL32P28, 5 more genes
    nsv6637880copy number variation1nstd102humanUncertain significance GRCh37 chr13: 56,897,737-64,074,025 , GRCh38.p12 chr13: 56,323,603-63,499,892 DIAPH3-AS2, LOC107984625, 64 more genes
    nsv6634793copy number variation1nstd227human GRCh37 chr13: 62,595,610-62,629,774 , GRCh38.p12 chr13: 62,021,477-62,055,641 LINC00358
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622074copy number variation1nstd224human GRCh37 chr13: 62,577,816-62,643,941 , GRCh38.p12 chr13: 62,003,683-62,069,808 LINC00358
    nsv6481998copy number variation1nstd223human GRCh38 chr13: 62,012,815-62,013,469 , GRCh37.p13 chr13: 62,586,948-62,587,602 LINC00358
    nsv6479554copy number variation1nstd223human GRCh38 chr13: 62,021,734-62,022,392 , GRCh37.p13 chr13: 62,595,867-62,596,525 LINC00358
    nsv6479400copy number variation1nstd223human GRCh38 chr13: 62,026,148-62,026,741 , GRCh37.p13 chr13: 62,600,281-62,600,874 LINC00358
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 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