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 347

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916843copy number variation1nstd209human GRCh38 chr9: 134,026,732-134,055,450 , GRCh37.p13 chr9: 136,891,854-136,920,572 LOC100130548, BRD3OS, 1 more genes
    nsv5861865copy number variation1nstd209human GRCh38 chr9: 134,026,574-134,028,873 , GRCh37.p13 chr9: 136,891,696-136,893,995 BRD3, BRD3OS
    nsv5858276copy number variation1nstd209human GRCh38 chr9: 134,024,841-134,030,554 , GRCh37.p13 chr9: 136,889,963-136,895,676 BRD3OS, BRD3
    nsv5854164copy number variation1nstd209human GRCh38 chr9: 134,042,596-134,045,802 , GRCh37.p13 chr9: 136,907,718-136,910,924 BRD3
    nsv5853435copy number variation1nstd209human GRCh38 chr9: 134,026,774-134,054,476 , GRCh37.p13 chr9: 136,891,896-136,919,598 BRD3OS, LOC100130548, 1 more genes
    nsv5852464copy number variation1nstd209human GRCh38 chr9: 134,037,646-134,043,268 , GRCh37.p13 chr9: 136,902,768-136,908,390 BRD3
    nsv5849427copy number variation1nstd209human GRCh38 chr9: 134,050,653-134,054,826 , GRCh37.p13 chr9: 136,915,775-136,919,948 BRD3, LOC100130548
    nsv5550009insertion1nstd206human GRCh38 chr9: 134,058,148-134,058,151 , GRCh37.p13 chr9: 136,923,270-136,923,273 LOC100130548, BRD3
    nsv5492080copy number variation1nstd206human GRCh38 chr9: 134,055,560-134,056,762 , GRCh37.p13 chr9: 136,920,682-136,921,884 BRD3, LOC100130548
    nsv5474523copy number variation1nstd206human GRCh38 chr9: 134,027,689-134,028,641 , GRCh37.p13 chr9: 136,892,811-136,893,763 BRD3OS, BRD3
    nsv5332041translocation1nstd200human GRCh37 chr9: 136,896,291-136,896,291 , GRCh37 chr14: 53,142,158-53,142,158 , GRCh38.p12 chr14: 52,675,440-52,675,440 , GRCh38.p12 chr9: 134,031,169-134,031,169 BRD3, ERO1A, 1 more genes
    nsv5329069translocation1nstd204human GRCh37.p13 chr9: 136,916,833-136,916,833 , GRCh37.p13 chr9: 136,917,427-136,917,427 , GRCh38.p13 chr9: 134,051,711-134,051,711 , GRCh38.p13 chr9: 134,052,305-134,052,305 BRD3, LOC100130548
    nsv5328535translocation1nstd204human GRCh38.p13 chr9: 134,036,031-134,036,031 , GRCh38.p13 chr9: 134,033,706-134,033,706 , GRCh37.p13 chr9: 136,898,828-136,898,828 , GRCh37.p13 chr9: 136,901,153-136,901,153 BRD3
    nsv5328306translocation1nstd204human GRCh38.p13 chr9: 134,051,558-134,051,558 , GRCh38.p13 chr9: 134,050,590-134,050,590 , GRCh37.p13 chr9: 136,916,680-136,916,680 , GRCh37.p13 chr9: 136,915,712-136,915,712 BRD3
    nsv5322734translocation1nstd204human GRCh37.p13 chr9: 136,915,713-136,915,713 , GRCh37.p13 chr9: 136,917,427-136,917,427 , GRCh38.p13 chr9: 134,050,591-134,050,591 , GRCh38.p13 chr9: 134,052,305-134,052,305 BRD3, LOC100130548
    nsv5321636translocation1nstd204human GRCh38.p13 chr9: 134,050,373-134,050,373 , GRCh38.p13 chr9: 134,048,456-134,048,456 , GRCh37.p13 chr9: 136,913,578-136,913,578 , GRCh37.p13 chr9: 136,915,495-136,915,495 BRD3
    nsv5321027translocation1nstd204human GRCh38.p13 chr9: 134,033,707-134,033,707 , GRCh38.p13 chr9: 134,034,700-134,034,700 , GRCh37.p13 chr9: 136,898,829-136,898,829 , GRCh37.p13 chr9: 136,899,822-136,899,822 BRD3
    nsv5124189mobile element insertion1nstd203human GRCh38 chr9: 134,057,024-134,057,032 , GRCh37.p13 chr9: 136,922,146-136,922,154 LOC100130548, BRD3
    nsv4985828copy number variation1nstd200human GRCh38 chr9: 134,026,732-134,055,452 , GRCh37.p13 chr9: 136,891,854-136,920,574 BRD3OS, LOC100130548, 1 more genes
    nsv4842303copy number variation1nstd200human GRCh37 chr9: 136,891,854-136,920,574 , GRCh38.p12 chr9: 134,026,732-134,055,452 BRD3OS, LOC100130548, 1 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