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 344

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965947insertion1nstd209human GRCh38 chr8: 123,354,864-123,354,864 , GRCh37.p13 chr8: 124,367,104-124,367,104 ATAD2
    nsv5964350insertion1nstd209human GRCh38 chr8: 123,382,618-123,382,618 , GRCh37.p13 chr8: 124,394,858-124,394,858 ATAD2
    nsv5950215insertion1nstd209human GRCh38 chr8: 123,377,091-123,377,091 , GRCh37.p13 chr8: 124,389,331-124,389,331 ATAD2
    nsv5922491copy number variation1nstd209human GRCh38 chr8: 123,330,626-123,331,069 , GRCh37.p13 chr8: 124,342,866-124,343,309 ATAD2
    nsv5919984copy number variation1nstd209human GRCh38 chr8: 123,381,433-123,384,012 , GRCh37.p13 chr8: 124,393,673-124,396,252 ATAD2
    nsv5918868copy number variation1nstd209human GRCh38 chr8: 123,353,026-123,353,322 , GRCh37.p13 chr8: 124,365,266-124,365,562 ATAD2, DUTP2
    nsv5914047copy number variation1nstd209human GRCh38 chr8: 123,383,661-123,383,968 , GRCh37.p13 chr8: 124,395,901-124,396,208 ATAD2
    nsv5854918copy number variation1nstd209human GRCh38 chr8: 123,381,661-123,383,817 , GRCh37.p13 chr8: 124,393,901-124,396,057 ATAD2
    nsv5491587copy number variation1nstd206human GRCh38 chr8: 123,376,447-123,377,016 , GRCh37.p13 chr8: 124,388,687-124,389,256 ATAD2
    nsv5479988copy number variation1nstd206human GRCh38 chr8: 123,352,151-123,352,277 , GRCh37.p13 chr8: 124,364,391-124,364,517 ATAD2, DUTP2
    nsv5379388translocation1nstd200human GRCh38 chr8: 123,330,097-123,330,097 , GRCh38 chr8: 123,330,210-123,330,210 , GRCh37.p13 chr8: 124,342,337-124,342,337 , GRCh37.p13 chr8: 124,342,450-124,342,450 ATAD2
    nsv5347368translocation1nstd200human GRCh38 chr12: 53,369,903-53,369,903 , GRCh38 chr8: 123,354,873-123,354,873 , GRCh37.p13 chr12: 53,763,687-53,763,687 , GRCh37.p13 chr8: 124,367,113-124,367,113 ATAD2
    nsv5304023copy number variation1nstd204human GRCh38.p13 chr8: 123,372,843-123,373,144 , GRCh37.p13 chr8: 124,385,083-124,385,384 ATAD2
    nsv5111966mobile element insertion1nstd203human GRCh38 chr8: 123,342,401-123,342,412 , GRCh37.p13 chr8: 124,354,641-124,354,652 ATAD2, RNU6-875P
    nsv5101869mobile element insertion1nstd203human GRCh38 chr8: 123,342,397-123,342,412 , GRCh37.p13 chr8: 124,354,637-124,354,652 ATAD2, RNU6-875P
    nsv5060033copy number variation1nstd102humanUncertain significance GRCh37 chr8: 121,938,227-125,485,728 , GRCh38.p12 chr8: 120,925,987-124,473,487 RNU6-756P, FAM83A, 53 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4827969copy number variation1nstd200human GRCh37 chr8: 124,395,925-124,396,193 , GRCh38.p12 chr8: 123,383,685-123,383,953 ATAD2
    nsv4827968copy number variation1nstd200human GRCh37 chr8: 124,342,883-124,343,313 , GRCh38.p12 chr8: 123,330,643-123,331,073 ATAD2
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 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