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 226

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976050insertion1nstd209human GRCh38 chr14: 92,071,010-92,071,010 , GRCh37.p13 chr14: 92,537,354-92,537,354 ATXN3
    nsv5967595insertion1nstd209human GRCh38 chr14: 92,061,803-92,061,803 , GRCh37.p13 chr14: 92,528,147-92,528,147 ATXN3
    nsv5706821mobile element insertion2nstd211human GRCh38 chr14: 92,070,760-92,070,760 , GRCh37.p13 chr14: 92,537,104-92,537,104 ATXN3
    nsv5694793mobile element insertion2nstd211human GRCh38 chr14: 92,096,166-92,096,166 , GRCh37.p13 chr14: 92,562,510-92,562,510 ATXN3
    nsv5663539insertion1nstd207human GRCh38 chr14: 92,071,009-92,071,009 , GRCh37.p13 chr14: 92,537,353-92,537,353 ATXN3
    nsv5657182insertion1nstd207human GRCh38 chr14: 92,073,408-92,073,408 , GRCh37.p13 chr14: 92,539,752-92,539,752 ATXN3
    nsv5656160insertion1nstd207human GRCh38 chr14: 92,060,270-92,060,270 , GRCh37.p13 chr14: 92,526,614-92,526,614 ATXN3
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , LINC00523, 713 more genes
    nsv5357546translocation1nstd200human GRCh38 chr14: 92,068,889-92,068,889 , GRCh38 chr14: 92,069,395-92,069,395 , GRCh37.p13 chr14: 92,535,233-92,535,233 , GRCh37.p13 chr14: 92,535,739-92,535,739 ATXN3
    nsv5149217mobile element insertion1nstd203human GRCh38 chr14: 92,073,408-92,073,425 , GRCh37.p13 chr14: 92,539,752-92,539,769 ATXN3
    nsv5143539mobile element insertion1nstd203human GRCh38 chr14: 92,059,447-92,059,464 , GRCh37.p13 chr14: 92,525,791-92,525,808 ATXN3
    nsv5004934copy number variation1nstd200human GRCh38 chr14: 91,569,497-92,338,399 , GRCh37.p13 chr14: 92,073,684-92,804,743 LOC101928957, FBLN5, 13 more genes
    nsv4863561copy number variation1nstd200human GRCh37 chr14: 92,035,841-92,804,743 , GRCh38.p12 chr14: 91,607,340-92,338,399 RNU6-366P, SLC24A4, 10 more genes
    nsv4849492copy number variation1nstd200human GRCh37 chr14: 92,534,503-92,534,574 , GRCh38.p12 chr14: 92,068,159-92,068,230 ATXN3
    nsv4753849insertion1nstd199human GRCh37 chr14: 92,537,352-92,537,352 , GRCh38.p12 chr14: 92,071,008-92,071,008 ATXN3
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 LOC105370644, EFCAB11, 175 more genes
    nsv4574937mobile element insertion1nstd166human GRCh37.p13 chr14: 92,541,193-92,541,193 , GRCh38.p12 chr14: 92,074,849-92,074,849 ATXN3
    nsv4548302insertion1nstd166human GRCh37.p13 chr14: 92,526,569-92,526,569 , GRCh38.p12 chr14: 92,060,225-92,060,225 ATXN3
    nsv4506816mobile element insertion1nstd166human GRCh37.p13 chr14: 92,539,752-92,539,752 , GRCh38.p12 chr14: 92,073,408-92,073,408 ATXN3
    nsv4505756mobile element insertion1nstd166human GRCh37.p13 chr14: 92,557,877-92,557,877 , GRCh38.p12 chr14: 92,091,533-92,091,533 ATXN3
    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