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 292

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977544insertion1nstd209human GRCh38 chr13: 100,656,560-100,656,560 , GRCh37.p13 chr13: 101,308,814-101,308,814 TMTC4
    nsv5944468copy number variation1nstd209human GRCh38 chr13: 100,619,015-100,619,190 , GRCh37.p13 chr13: 101,271,269-101,271,444 TMTC4
    nsv5931521copy number variation1nstd209human GRCh38 chr13: 100,607,526-100,607,690 , GRCh37.p13 chr13: 101,259,780-101,259,944 TMTC4
    nsv5672807copy number variation1nstd102humanPathogenic GRCh37 chr13: 92,002,837-103,343,314 , GRCh38.p12 chr13: 91,350,583-102,690,964 RPL7L1P12, MIR548AS, 153 more genes
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5645788insertion1nstd207human GRCh38 chr13: 100,615,041-100,615,041 , GRCh37.p13 chr13: 101,267,295-101,267,295 TMTC4
    nsv5588387copy number variation1nstd207human GRCh38 chr13: 100,607,526-100,607,690 , GRCh37.p13 chr13: 101,259,780-101,259,944 TMTC4
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5512835copy number variation1nstd206human GRCh38 chr13: 100,607,527-100,607,691 , GRCh37.p13 chr13: 101,259,781-101,259,945 TMTC4
    nsv5503923copy number variation1nstd206human GRCh38 chr13: 100,615,568-100,616,368 , GRCh37.p13 chr13: 101,267,822-101,268,622 TMTC4
    nsv5498545copy number variation1nstd206human GRCh38 chr13: 100,669,402-100,672,937 , GRCh37.p13 chr13: 101,321,656-101,325,191 TMTC4
    nsv5374375translocation1nstd200human GRCh38 chr13: 100,615,660-100,615,660 , GRCh38 chr13: 100,616,368-100,616,368 , GRCh37.p13 chr13: 101,267,914-101,267,914 , GRCh37.p13 chr13: 101,268,622-101,268,622 TMTC4
    nsv5348895translocation1nstd200human GRCh38 chr13: 100,636,357-100,636,357 , GRCh38 chr13: 100,636,433-100,636,433 , GRCh37.p13 chr13: 101,288,611-101,288,611 , GRCh37.p13 chr13: 101,288,687-101,288,687 TMTC4
    nsv5306806copy number variation1nstd204human GRCh38.p13 chr13: 100,615,660-100,616,381 , GRCh37.p13 chr13: 101,267,914-101,268,635 TMTC4
    nsv5212397mobile element deletion1nstd204human GRCh38.p13 chr13: 100,644,091-100,644,411 , GRCh37.p13 chr13: 101,296,345-101,296,665 TMTC4
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4998437copy number variation1nstd200human GRCh38 chr13: 100,645,875-100,649,683 , GRCh37.p13 chr13: 101,298,129-101,301,937 TMTC4
    nsv4993921copy number variation1nstd200human GRCh38 chr13: 100,611,372-100,633,202 , GRCh37.p13 chr13: 101,263,626-101,285,456 TMTC4, COX5BP6
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4845256copy number variation1nstd200human GRCh37 chr13: 101,267,915-101,268,621 , GRCh38.p12 chr13: 100,615,661-100,616,367 TMTC4
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center