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 387

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960881insertion1nstd209human GRCh38 chr3: 10,070,476-10,070,476 , GRCh37.p13 chr3: 10,112,160-10,112,160 FANCD2
    nsv5952131insertion1nstd209human GRCh38 chr3: 10,036,105-10,036,105 , GRCh37.p13 chr3: 10,077,789-10,077,789 FANCD2, RNU6-670P
    nsv5904127copy number variation1nstd209human GRCh38 chr3: 9,996,659-11,875,087 , GRCh37.p13 chr3: 10,038,343-11,916,561 , EMC3, 35 more genes
    nsv5902924copy number variation1nstd209human GRCh38 chr3: 10,045,650-10,046,101 , GRCh37.p13 chr3: 10,087,334-10,087,785 FANCD2
    nsv5901270copy number variation1nstd209human GRCh38 chr3: 10,048,544-11,870,471 , GRCh37.p13 chr3: 10,090,228-11,911,945 , SLC6A11, 29 more genes
    nsv5891525copy number variation1nstd209human GRCh38 chr3: 9,996,478-11,874,953 , GRCh37.p13 chr3: 10,038,162-11,916,427 , TATDN2, 35 more genes
    nsv5888016copy number variation1nstd209human GRCh38 chr3: 9,994,085-10,047,814 , GRCh37.p13 chr3: 10,035,769-10,089,498 FANCD2, EMC3, 6 more genes
    nsv5673714copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,094,065-10,094,065 , GRCh38.p12 chr3: 10,052,381-10,052,381 FANCD2
    nsv5673636copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,074,510-10,085,282 , GRCh38.p12 chr3: 10,032,826-10,043,598 FANCD2, RNU6-670P
    nsv5673556copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 10,084,233-10,085,286 , GRCh38.p12 chr3: 10,042,549-10,043,602 FANCD2
    nsv5673552copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,106,407-10,106,407 , GRCh38.p12 chr3: 10,064,723-10,064,723 FANCD2
    nsv5673471copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 10,091,048-10,140,634 , GRCh38.p12 chr3: 10,049,364-10,098,950 FANCD2, FANCD2OS, 1 more genes
    nsv5673470copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,070,342-10,074,666 , GRCh38.p12 chr3: 10,028,658-10,032,982 FANCD2
    nsv5623692insertion1nstd207human GRCh38 chr3: 10,069,493-10,069,493 , GRCh37.p13 chr3: 10,111,177-10,111,177 FANCD2
    nsv5617608insertion1nstd207human GRCh38 chr3: 10,070,476-10,070,476 , GRCh37.p13 chr3: 10,112,160-10,112,160 FANCD2
    nsv5612940insertion1nstd207human GRCh38 chr3: 10,070,538-10,070,538 , GRCh37.p13 chr3: 10,112,222-10,112,222 FANCD2
    nsv5604733insertion1nstd207human GRCh38 chr3: 10,069,478-10,069,478 , GRCh37.p13 chr3: 10,111,162-10,111,162 FANCD2
    nsv5449283copy number variation1nstd206human GRCh38 chr3: 10,093,566-10,093,631 , GRCh37.p13 chr3: 10,135,250-10,135,315 FANCD2OS, FANCD2
    nsv5444112copy number variation1nstd206human GRCh38 chr3: 10,084,219-10,085,669 , GRCh37.p13 chr3: 10,125,903-10,127,353 FANCD2OS, FANCD2
    nsv5435890copy number variation1nstd206human GRCh38 chr3: 10,025,800-10,025,992 , GRCh37.p13 chr3: 10,067,484-10,067,676 FANCD2, CIDECP1
    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