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 439

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5729875mobile element insertion1nstd211human GRCh38 chr1: 180,044,002-180,044,002 , GRCh37.p13 chr1: 180,013,137-180,013,137 CEP350
    nsv5721404mobile element insertion1nstd211human GRCh38 chr1: 180,067,073-180,067,073 , GRCh37.p13 chr1: 180,036,208-180,036,208 CEP350
    nsv5720474mobile element insertion1nstd211human GRCh38 chr1: 180,071,642-180,071,642 , GRCh37.p13 chr1: 180,040,777-180,040,777 CEP350
    nsv5683745mobile element insertion2nstd211human GRCh38 chr1: 180,102,647-180,102,647 , GRCh37.p13 chr1: 180,071,782-180,071,782 CEP350
    nsv5680380mobile element insertion1nstd211human GRCh38 chr1: 180,079,527-180,079,527 , GRCh37.p13 chr1: 180,048,662-180,048,662 CEP350
    nsv5614670insertion1nstd207human GRCh38 chr1: 180,079,515-180,079,515 , GRCh37.p13 chr1: 180,048,650-180,048,650 CEP350
    nsv5559093mobile element insertion1nstd206human GRCh38 chr1: 180,071,642-180,071,693 , GRCh37.p13 chr1: 180,040,777-180,040,828 CEP350
    nsv5428287copy number variation1nstd206human GRCh38 chr1: 179,961,913-179,970,533 , GRCh37.p13 chr1: 179,931,048-179,939,668 RPSAP16, CEP350
    nsv5420365copy number variation1nstd206human GRCh38 chr1: 179,981,762-179,981,876 , GRCh37.p13 chr1: 179,950,897-179,951,011 CEP350
    nsv5402617mobile element insertion1nstd206human GRCh38 chr1: 180,079,527-180,079,578 , GRCh37.p13 chr1: 180,048,662-180,048,713 CEP350
    nsv5400613mobile element insertion1nstd206human GRCh38 chr1: 180,102,647-180,102,698 , GRCh37.p13 chr1: 180,071,782-180,071,833 CEP350
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5379282translocation1nstd200human GRCh38 chr1: 180,002,456-180,002,456 , GRCh38 chr1: 180,006,674-180,006,674 , GRCh37.p13 chr1: 179,971,591-179,971,591 , GRCh37.p13 chr1: 179,975,809-179,975,809 CEP350
    nsv5347343translocation1nstd200human GRCh38 chr1: 180,002,350-180,002,350 , GRCh38 chr1: 180,006,186-180,006,186 , GRCh37.p13 chr1: 179,975,321-179,975,321 , GRCh37.p13 chr1: 179,971,485-179,971,485 CEP350
    nsv5347342translocation1nstd200human GRCh38 chr1: 179,961,913-179,961,913 , GRCh38 chr1: 179,970,533-179,970,533 , GRCh37.p13 chr1: 179,939,668-179,939,668 , GRCh37.p13 chr1: 179,931,048-179,931,048 CEP350
    nsv5287165copy number variation1nstd204human GRCh38.p13 chr1: 179,953,028-179,966,035 , GRCh37.p13 chr1: 179,922,163-179,935,170 LOC101928933, CEP350
    nsv5210313copy number variation1nstd204human GRCh38.p13 chr1: 179,954,674-179,964,667 , GRCh37.p13 chr1: 179,923,809-179,933,802 LOC101928933, CEP350
    nsv5077062mobile element insertion1nstd203human GRCh38 chr1: 180,102,633-180,102,647 , GRCh37.p13 chr1: 180,071,768-180,071,782 CEP350
    nsv5073708mobile element insertion1nstd203human GRCh38 chr1: 180,030,203-180,030,214 , GRCh37.p13 chr1: 179,999,338-179,999,349 CEP350
    nsv5068662mobile element insertion1nstd203human GRCh38 chr1: 180,079,421-180,079,436 , GRCh37.p13 chr1: 180,048,556-180,048,571 CEP350
    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