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 655

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130287mobile element insertion1nstd186human GRCh37 chr13: 42,771,403-42,771,447 , GRCh38.p12 chr13: 42,197,267-42,197,311 DGKH
    nsv6114187mobile element insertion1nstd186human GRCh37 chr13: 42,726,786-42,726,786 , GRCh38.p12 chr13: 42,152,650-42,152,650 DGKH
    nsv5975128insertion1nstd209human GRCh38 chr13: 42,197,255-42,197,255 , GRCh37.p13 chr13: 42,771,391-42,771,391 DGKH
    nsv5974638insertion1nstd209human GRCh38 chr13: 42,152,650-42,152,650 , GRCh37.p13 chr13: 42,726,786-42,726,786 DGKH
    nsv5973094inversion1nstd209human GRCh38 chr13: 42,151,478-42,151,609 , GRCh37.p13 chr13: 42,725,614-42,725,745 DGKH
    nsv5968083insertion1nstd209human GRCh38 chr13: 42,159,244-42,159,244 , GRCh37.p13 chr13: 42,733,380-42,733,380 DGKH
    nsv5935941copy number variation1nstd209human GRCh38 chr13: 42,094,283-42,107,019 , GRCh37.p13 chr13: 42,668,419-42,681,155 DGKH
    nsv5934352copy number variation1nstd209human GRCh38 chr13: 42,181,816-42,182,067 , GRCh37.p13 chr13: 42,755,952-42,756,203 CHCHD2P11, DGKH
    nsv5933120copy number variation1nstd209human GRCh38 chr13: 42,184,120-42,185,189 , GRCh37.p13 chr13: 42,758,256-42,759,325 DGKH
    nsv5928954copy number variation1nstd209human GRCh38 chr13: 42,104,861-42,105,160 , GRCh37.p13 chr13: 42,678,997-42,679,296 DGKH
    nsv5855080copy number variation1nstd209human GRCh38 chr13: 42,094,342-42,103,824 , GRCh37.p13 chr13: 42,668,478-42,677,960 DGKH
    nsv5723734mobile element insertion1nstd211human GRCh38 chr13: 42,256,741-42,256,741 , GRCh37.p13 chr13: 42,830,877-42,830,877 DGKH, FHP1
    nsv5719644mobile element insertion2nstd211human GRCh38 chr13: 42,197,267-42,197,267 , GRCh37.p13 chr13: 42,771,403-42,771,403 DGKH
    nsv5717511mobile element insertion1nstd211human GRCh38 chr13: 42,137,868-42,137,868 , GRCh37.p13 chr13: 42,712,004-42,712,004 DGKH
    nsv5712944mobile element insertion2nstd211human GRCh38 chr13: 42,125,938-42,125,938 , GRCh37.p13 chr13: 42,700,074-42,700,074 DGKH
    nsv5708586mobile element insertion1nstd211human GRCh38 chr13: 42,191,122-42,191,122 , GRCh37.p13 chr13: 42,765,258-42,765,258 DGKH
    nsv5697663mobile element insertion2nstd211human GRCh38 chr13: 42,152,665-42,152,665 , GRCh37.p13 chr13: 42,726,801-42,726,801 DGKH
    nsv5663798insertion1nstd207human GRCh38 chr13: 42,197,252-42,197,252 , GRCh37.p13 chr13: 42,771,388-42,771,388 DGKH
    nsv5656682insertion1nstd207human GRCh38 chr13: 42,152,650-42,152,650 , GRCh37.p13 chr13: 42,726,786-42,726,786 DGKH
    nsv5652380insertion1nstd207human GRCh38 chr13: 42,151,533-42,151,533 , GRCh37.p13 chr13: 42,725,669-42,725,669 DGKH
    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