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 577

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960518insertion1nstd209human GRCh38 chr7: 51,098,224-51,098,224 , GRCh37.p13 chr7: 51,165,921-51,165,921 COBL
    nsv5958722insertion1nstd209human GRCh38 chr7: 51,018,906-51,018,906 , GRCh37.p13 chr7: 51,086,603-51,086,603 COBL
    nsv5925105copy number variation1nstd209human GRCh38 chr7: 51,288,776-51,288,866 , GRCh37.p13 chr7: 51,356,473-51,356,563 COBL
    nsv5921329copy number variation1nstd209human GRCh38 chr7: 51,093,999-51,097,700 , GRCh37.p13 chr7: 51,161,696-51,165,397 COBL
    nsv5917521copy number variation1nstd209human GRCh38 chr7: 51,315,697-51,315,950 , GRCh37.p13 chr7: 51,383,394-51,383,647 COBL
    nsv5914559copy number variation1nstd209human GRCh38 chr7: 51,203,205-51,203,474 , GRCh37.p13 chr7: 51,270,902-51,271,171 COBL
    nsv5910629copy number variation1nstd209human GRCh38 chr7: 51,257,606-51,258,234 , GRCh37.p13 chr7: 51,325,303-51,325,931 COBL, RPL7L1P2
    nsv5846895copy number variation1nstd209human GRCh38 chr7: 51,094,049-51,097,698 , GRCh37.p13 chr7: 51,161,746-51,165,395 COBL
    nsv5684143mobile element insertion1nstd211human GRCh38 chr7: 51,236,815-51,236,815 , GRCh37.p13 chr7: 51,304,512-51,304,512 COBL
    nsv5681699mobile element insertion1nstd211human GRCh38 chr7: 51,248,631-51,248,631 , GRCh37.p13 chr7: 51,316,328-51,316,328 COBL
    nsv5679273mobile element insertion1nstd211human GRCh38 chr7: 51,151,486-51,151,486 , GRCh37.p13 chr7: 51,219,183-51,219,183 COBL
    nsv5676615mobile element insertion2nstd211human GRCh38 chr7: 51,098,236-51,098,236 , GRCh37.p13 chr7: 51,165,933-51,165,933 COBL
    nsv5583083copy number variation1nstd207human GRCh38 chr7: 51,288,788-51,288,879 , GRCh37.p13 chr7: 51,356,485-51,356,576 COBL
    nsv5574602copy number variation1nstd207human GRCh38 chr7: 51,208,375-51,208,424 , GRCh37.p13 chr7: 51,276,072-51,276,121 COBL
    nsv5573022copy number variation1nstd207human GRCh38 chr7: 51,203,205-51,203,474 , GRCh37.p13 chr7: 51,270,902-51,271,171 COBL
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5540103insertion1nstd206human GRCh38 chr7: 51,224,698-51,224,733 , GRCh37.p13 chr7: 51,292,395-51,292,430 COBL
    nsv5493582copy number variation1nstd206human GRCh38 chr7: 51,288,776-51,288,884 , GRCh37.p13 chr7: 51,356,473-51,356,581 COBL
    nsv5490805copy number variation1nstd206human GRCh38 chr7: 51,119,191-51,119,258 , GRCh37.p13 chr7: 51,186,888-51,186,955 COBL
    nsv5487900copy number variation1nstd206human GRCh38 chr7: 51,315,700-51,315,951 , GRCh37.p13 chr7: 51,383,397-51,383,648 COBL
    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