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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885478copy number variation1nstd209human GRCh38 chr1: 32,081,050-32,081,102 , GRCh37.p13 chr1: 32,546,651-32,546,703 TMEM39B
    nsv5881935copy number variation1nstd209human GRCh38 chr1: 32,088,832-32,090,720 , GRCh37.p13 chr1: 32,554,433-32,556,321 TMEM39B
    nsv5876889copy number variation1nstd209human GRCh38 chr1: 32,085,503-32,087,373 , GRCh37.p13 chr1: 32,551,104-32,552,974 TMEM39B, MIR5585
    nsv5876839copy number variation1nstd209human GRCh38 chr1: 32,070,397-32,072,003 , GRCh37.p13 chr1: 32,535,998-32,537,604 TMEM39B
    nsv5830290copy number variation1nstd209human GRCh38 chr1: 32,088,794-32,090,693 , GRCh37.p13 chr1: 32,554,395-32,556,294 TMEM39B
    nsv5829988copy number variation1nstd209human GRCh38 chr1: 32,084,092-32,087,975 , GRCh37.p13 chr1: 32,549,693-32,553,576 MIR5585, TMEM39B
    nsv5829695copy number variation1nstd209human GRCh38 chr1: 32,085,467-32,087,574 , GRCh37.p13 chr1: 32,551,068-32,553,175 MIR5585, TMEM39B
    nsv5686487mobile element insertion2nstd211human GRCh38 chr1: 32,088,772-32,088,772 , GRCh37.p13 chr1: 32,554,373-32,554,373 TMEM39B
    nsv5431898copy number variation1nstd206human GRCh38 chr1: 32,088,772-32,090,673 , GRCh37.p13 chr1: 32,554,373-32,556,274 TMEM39B
    nsv5431127copy number variation1nstd206human GRCh38 chr1: 32,083,331-32,083,670 , GRCh37.p13 chr1: 32,548,932-32,549,271 TMEM39B
    nsv5429233copy number variation1nstd206human GRCh38 chr1: 32,085,520-32,087,351 , GRCh37.p13 chr1: 32,551,121-32,552,952 MIR5585, TMEM39B
    nsv5427309copy number variation1nstd206human GRCh38 chr1: 32,083,530-32,090,747 , GRCh37.p13 chr1: 32,549,131-32,556,348 TMEM39B, MIR5585
    nsv5424270copy number variation1nstd206human GRCh38 chr1: 32,070,397-32,072,004 , GRCh37.p13 chr1: 32,535,998-32,537,605 TMEM39B
    nsv5423357copy number variation1nstd206human GRCh38 chr1: 32,082,586-32,087,762 , GRCh37.p13 chr1: 32,548,187-32,553,363 MIR5585, TMEM39B
    nsv5419336copy number variation1nstd206human GRCh38 chr1: 32,078,850-32,083,006 , GRCh37.p13 chr1: 32,544,451-32,548,607 TMEM39B
    nsv5361100translocation1nstd200human GRCh38 chr1: 32,086,437-32,086,437 , GRCh38 chr1: 32,086,363-32,086,363 , GRCh37.p13 chr1: 32,551,964-32,551,964 , GRCh37.p13 chr1: 32,552,038-32,552,038 MIR5585, TMEM39B
    nsv5289800copy number variation1nstd204human GRCh38.p13 chr1: 32,088,743-32,090,724 , GRCh37.p13 chr1: 32,554,344-32,556,325 TMEM39B
    nsv5217268mobile element deletion1nstd204human GRCh38.p13 chr1: 32,093,391-32,093,711 , GRCh37.p13 chr1: 32,558,992-32,559,312 TMEM39B
    nsv5216521copy number variation1nstd204human GRCh38.p13 chr1: 32,087,976-32,090,393 , GRCh37.p13 chr1: 32,553,577-32,555,994 TMEM39B
    nsv5213456copy number variation1nstd204human GRCh38.p13 chr1: 31,802,501-32,105,200 , GRCh37.p13 chr1: 32,268,102-32,570,801 TMEM39B, KHDRBS1, 3 more genes
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