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 203

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120675copy number variation1nstd186human GRCh37 chr16: 67,253,676-67,253,981 , GRCh38.p12 chr16: 67,219,773-67,220,078 FBXL9P
    nsv5943633copy number variation1nstd209human GRCh38 chr16: 67,219,762-67,220,077 , GRCh37.p13 chr16: 67,253,665-67,253,980 FBXL9P
    nsv5647040insertion1nstd207human GRCh38 chr16: 67,209,395-67,209,395 , GRCh37.p13 chr16: 67,243,298-67,243,298 FBXL9P
    nsv5600171copy number variation1nstd207human GRCh38 chr16: 67,219,762-67,220,077 , GRCh37.p13 chr16: 67,253,665-67,253,980 FBXL9P
    nsv5533342copy number variation1nstd206human GRCh38 chr16: 67,218,892-67,219,587 , GRCh37.p13 chr16: 67,252,795-67,253,490 FBXL9P
    nsv5532090copy number variation1nstd206human GRCh38 chr16: 67,223,660-67,225,381 , GRCh37.p13 chr16: 67,257,563-67,259,284 FBXL9P, TMEM208
    nsv5520293copy number variation1nstd206human GRCh38 chr16: 67,219,773-67,220,078 , GRCh37.p13 chr16: 67,253,676-67,253,981 FBXL9P
    nsv5383052mobile element deletion2nstd186human GRCh37 chr16: 67,253,676-67,253,981 , GRCh38.p12 chr16: 67,219,773-67,220,078 FBXL9P
    nsv5271417copy number variation1nstd204human GRCh38.p13 chr16: 67,219,801-67,220,100 , GRCh37.p13 chr16: 67,253,704-67,254,003 FBXL9P
    nsv5211384mobile element deletion1nstd204human GRCh38.p13 chr16: 67,219,773-67,220,078 , GRCh37.p13 chr16: 67,253,676-67,253,981 FBXL9P
    nsv5141102mobile element insertion1nstd203human GRCh38 chr16: 67,221,991-67,222,024 , GRCh37.p13 chr16: 67,255,894-67,255,927 FBXL9P
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005780copy number variation1nstd200human GRCh38 chr16: 67,159,261-67,221,610 , GRCh37.p13 chr16: 67,193,164-67,255,513 TRADD, HSF4, 8 more genes
    nsv5005779copy number variation1nstd200human GRCh38 chr16: 67,159,176-67,212,734 , GRCh37.p13 chr16: 67,193,079-67,246,637 EXOC3L1, FBXL9P, 8 more genes
    nsv4993094copy number variation1nstd200human GRCh38 chr16: 67,223,232-67,224,715 , GRCh37.p13 chr16: 67,257,135-67,258,618 FBXL9P
    nsv4993093copy number variation1nstd200human GRCh38 chr16: 67,202,558-67,205,520 , GRCh37.p13 chr16: 67,236,461-67,239,423 ELMO3, FBXL9P, 1 more genes
    nsv4900168mobile element deletion1nstd200human GRCh38 chr16: 67,219,773-67,220,078 , GRCh37.p13 chr16: 67,253,676-67,253,981 FBXL9P
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4857468copy number variation1nstd200human GRCh37 chr16: 67,255,819-67,256,105 , GRCh38.p12 chr16: 67,221,916-67,222,202 FBXL9P
    nsv4786103mobile element deletion1nstd200human GRCh37 chr16: 67,253,676-67,253,981 , GRCh38.p12 chr16: 67,219,773-67,220,078 FBXL9P
    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