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 427

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120287copy number variation1nstd186human GRCh37 chr6: 132,707,435-132,712,421 , GRCh38.p12 chr6: 132,386,296-132,391,282 MOXD1
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
    nsv5905416copy number variation1nstd209human GRCh38 chr6: 132,376,489-132,376,811 , GRCh37.p13 chr6: 132,697,628-132,697,950 MOXD1
    nsv5900350copy number variation1nstd209human GRCh38 chr6: 132,338,046-132,338,220 , GRCh37.p13 chr6: 132,659,185-132,659,359 MOXD1
    nsv5897550copy number variation1nstd209human GRCh38 chr6: 132,386,333-132,391,238 , GRCh37.p13 chr6: 132,707,472-132,712,377 MOXD1
    nsv5894055copy number variation1nstd209human GRCh38 chr6: 132,370,026-132,370,391 , GRCh37.p13 chr6: 132,691,165-132,691,530 MOXD1
    nsv5844282copy number variation1nstd209human GRCh38 chr6: 132,353,310-132,359,656 , GRCh37.p13 chr6: 132,674,449-132,680,795 MOXD1
    nsv5844027copy number variation1nstd209human GRCh38 chr6: 132,386,386-132,391,282 , GRCh37.p13 chr6: 132,707,525-132,712,421 MOXD1
    nsv5717534mobile element insertion1nstd211human GRCh38 chr6: 132,366,436-132,366,436 , GRCh37.p13 chr6: 132,687,575-132,687,575 MOXD1
    nsv5583161copy number variation1nstd207human GRCh38 chr6: 132,376,489-132,376,811 , GRCh37.p13 chr6: 132,697,628-132,697,950 MOXD1
    nsv5581289copy number variation1nstd207human GRCh38 chr6: 132,386,421-132,391,278 , GRCh37.p13 chr6: 132,707,560-132,712,417 MOXD1
    nsv5577377copy number variation1nstd207human GRCh38 chr6: 132,349,402-132,349,451 , GRCh37.p13 chr6: 132,670,541-132,670,590 MOXD1
    nsv5576139copy number variation1nstd207human GRCh38 chr6: 132,386,028-132,386,326 , GRCh37.p13 chr6: 132,707,167-132,707,465 MOXD1
    nsv5562222mobile element insertion1nstd206human GRCh38 chr6: 132,366,436-132,366,487 , GRCh37.p13 chr6: 132,687,575-132,687,626 MOXD1
    nsv5473163copy number variation1nstd206human GRCh38 chr6: 132,358,316-132,358,392 , GRCh37.p13 chr6: 132,679,455-132,679,531 MOXD1
    nsv5472888copy number variation1nstd206human GRCh38 chr6: 132,376,503-132,376,812 , GRCh37.p13 chr6: 132,697,642-132,697,951 MOXD1
    nsv5471051copy number variation1nstd206human GRCh38 chr6: 132,338,042-132,338,230 , GRCh37.p13 chr6: 132,659,181-132,659,369 MOXD1
    nsv5466428copy number variation1nstd206human GRCh38 chr6: 132,314,608-132,314,686 , GRCh37.p13 chr6: 132,635,747-132,635,825 MOXD1
    nsv5462487copy number variation1nstd206human GRCh38 chr6: 132,303,802-132,303,947 , GRCh37.p13 chr6: 132,624,941-132,625,086 MOXD1
    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