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 529

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098327copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,681,834-71,681,968 , GRCh38.p12 chrX: 72,461,984-72,462,118 HDAC8
    nsv7088777copy number variation1nstd229human GRCh38 chrX: 72,568,245-72,568,622 , GRCh37.p13 chrX|NW_004070882.1: 257,262-257,639 , GRCh37.p13 chrX: 71,788,095-71,788,472 HDAC8
    nsv7088776copy number variation1nstd229human GRCh38 chrX: 72,557,974-72,664,545 , GRCh37.p13 chrX|NW_004070882.1: 246,991-353,562 , GRCh37.p13 chrX: 71,777,824-71,884,395 MATR3P1, PHKA1, 1 more genes
    nsv7088775copy number variation1nstd229human GRCh38 chrX: 72,529,785-72,529,864 , GRCh37.p13 chrX|NW_004070882.1: 218,802-218,881 , GRCh37.p13 chrX: 71,749,635-71,749,714 HDAC8
    nsv7088774copy number variation1nstd229human GRCh38 chrX: 72,527,565-72,533,093 , GRCh37.p13 chrX|NW_004070882.1: 216,582-222,110 , GRCh37.p13 chrX: 71,747,415-71,752,943 HDAC8
    nsv7088773copy number variation1nstd229human GRCh38 chrX: 72,486,501-72,488,400 , GRCh37.p13 chrX|NW_004070882.1: 175,518-177,417 , GRCh37.p13 chrX: 71,706,351-71,708,250 HDAC8
    nsv7088772copy number variation1nstd229human GRCh38 chrX: 72,433,083-72,451,696 , GRCh37.p13 chrX: 71,652,933-71,671,546 , GRCh37.p13 chrX|NW_004070882.1: 122,100-140,713 HDAC8
    nsv7088771copy number variation1nstd229human GRCh38 chrX: 72,423,426-72,429,525 , GRCh37.p13 chrX|NW_004070882.1: 112,443-118,542 , GRCh37.p13 chrX: 71,643,276-71,649,375 HDAC8
    nsv7088770copy number variation1nstd229human GRCh38 chrX: 72,411,441-72,422,190 , GRCh37.p13 chrX|NW_004070882.1: 100,458-111,207 , GRCh37.p13 chrX: 71,631,291-71,642,040 HDAC8
    nsv7088769copy number variation1nstd229human GRCh38 chrX: 72,409,352-72,412,832 , GRCh37.p13 chrX|NW_004070882.1: 98,369-101,849 , GRCh37.p13 chrX: 71,629,202-71,632,682 HDAC8
    nsv7088768copy number variation1nstd229human GRCh38 chrX: 72,392,820-72,393,599 , GRCh37.p13 chrX: 71,612,670-71,613,449 , GRCh37.p13 chrX|NW_004070882.1: 81,837-82,616 HDAC8
    nsv7088767copy number variation1nstd229human GRCh38 chrX: 72,391,424-72,399,719 , GRCh37.p13 chrX|NW_004070882.1: 80,441-88,736 , GRCh37.p13 chrX: 71,611,274-71,619,569 HDAC8
    nsv7088766copy number variation1nstd229human GRCh38 chrX: 72,389,623-72,389,988 , GRCh37.p13 chrX|NW_004070882.1: 78,640-79,005 , GRCh37.p13 chrX: 71,609,473-71,609,838 HDAC8
    nsv7088765copy number variation1nstd229human GRCh38 chrX: 72,387,944-72,391,014 , GRCh37.p13 chrX|NW_004070882.1: 76,961-80,031 , GRCh37.p13 chrX: 71,607,794-71,610,864 HDAC8
    nsv7088764copy number variation1nstd229human GRCh38 chrX: 72,378,412-72,382,765 , GRCh37.p13 chrX|NW_004070882.1: 67,429-71,782 , GRCh37.p13 chrX: 71,598,262-71,602,615 HDAC8
    nsv7088763copy number variation1nstd229human GRCh38 chrX: 72,372,075-72,388,011 , GRCh37.p13 chrX|NW_004070882.1: 61,092-77,028 , GRCh37.p13 chrX: 71,591,925-71,607,861 RNU2-68P, HDAC8
    nsv7088762copy number variation1nstd229human GRCh38 chrX: 72,341,340-72,341,501 , GRCh37.p13 chrX|NW_004070882.1: 30,357-30,518 , GRCh37.p13 chrX: 71,561,190-71,561,351 HDAC8
    nsv7088761copy number variation1nstd229human GRCh38 chrX: 72,335,852-72,341,058 , GRCh37.p13 chrX|NW_004070882.1: 24,869-30,075 , GRCh37.p13 chrX: 71,555,702-71,560,908 HDAC8
    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