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 815

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044478inversion1nstd229human GRCh38 chr3: 140,992,844-142,136,153 , GRCh37.p13 chr3: 140,711,686-141,854,995 KRT18P35, SPSB4, 16 more genes
    nsv7044167inversion1nstd229human GRCh38 chr3: 142,085,550-142,089,420 , GRCh37.p13 chr3: 141,804,392-141,808,262 TFDP2
    nsv7039503inversion1nstd229human GRCh38 chr3: 142,018,944-142,019,048 , GRCh37.p13 chr3: 141,737,786-141,737,890 TFDP2
    nsv6737691copy number variation1nstd229human GRCh38 chr3: 142,148,501-142,204,500 , GRCh37.p13 chr3: 141,867,343-141,923,342 GK5, TFDP2
    nsv6737539copy number variation1nstd229human GRCh38 chr3: 142,126,833-142,126,878 , GRCh37.p13 chr3: 141,845,675-141,845,720 TFDP2
    nsv6735964copy number variation1nstd229human GRCh38 chr3: 142,130,910-142,133,645 , GRCh37.p13 chr3: 141,849,752-141,852,487 TFDP2
    nsv6735124copy number variation1nstd229human GRCh38 chr3: 142,116,180-142,121,546 , GRCh37.p13 chr3: 141,835,022-141,840,388 TFDP2
    nsv6733771copy number variation1nstd229human GRCh38 chr3: 142,139,850-142,140,353 , GRCh37.p13 chr3: 141,858,692-141,859,195 TFDP2
    nsv6733328copy number variation1nstd229human GRCh38 chr3: 142,129,667-142,137,182 , GRCh37.p13 chr3: 141,848,509-141,856,024 TFDP2
    nsv6731755copy number variation1nstd229human GRCh38 chr3: 141,757,101-142,395,000 , GRCh37.p13 chr3: 141,475,943-142,113,842 RNU6-509P, RNU6-425P, 8 more genes
    nsv6730680copy number variation1nstd229human GRCh38 chr3: 142,067,706-142,070,965 , GRCh37.p13 chr3: 141,786,548-141,789,807 TFDP2
    nsv6730524copy number variation1nstd229human GRCh38 chr3: 142,065,169-142,070,147 , GRCh37.p13 chr3: 141,784,011-141,788,989 TFDP2
    nsv6730402copy number variation1nstd229human GRCh38 chr3: 142,118,523-142,146,126 , GRCh37.p13 chr3: 141,837,365-141,864,968 RNU6-425P, TFDP2
    nsv6729549copy number variation1nstd229human GRCh38 chr3: 142,130,901-142,133,100 , GRCh37.p13 chr3: 141,849,743-141,851,942 TFDP2
    nsv6727341copy number variation1nstd229human GRCh38 chr3: 142,107,101-142,349,700 , GRCh37.p13 chr3: 141,825,943-142,068,542 GK5, XRN1, 2 more genes
    nsv6724599copy number variation1nstd229human GRCh38 chr3: 142,036,773-142,040,850 , GRCh37.p13 chr3: 141,755,615-141,759,692 TFDP2
    nsv6724455copy number variation1nstd229human GRCh38 chr3: 142,051,286-142,052,285 , GRCh37.p13 chr3: 141,770,128-141,771,127 TFDP2
    nsv6723016copy number variation1nstd229human GRCh38 chr3: 142,021,372-142,022,605 , GRCh37.p13 chr3: 141,740,214-141,741,447 TFDP2
    nsv6721803copy number variation1nstd229human GRCh38 chr3: 141,965,122-141,966,999 , GRCh37.p13 chr3: 141,683,964-141,685,841 TFDP2
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 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