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 202

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5724934mobile element insertion1nstd211human GRCh38 chr2: 10,440,382-10,440,382 , GRCh37.p13 chr2: 10,580,508-10,580,508 ODC1
    nsv5554400mobile element insertion1nstd206human GRCh38 chr2: 10,440,332-10,440,382 , GRCh37.p13 chr2: 10,580,458-10,580,508 ODC1
    nsv5452274copy number variation1nstd206human GRCh38 chr2: 10,441,725-10,441,816 , GRCh37.p13 chr2: 10,581,851-10,581,942 ODC1
    nsv5451896copy number variation1nstd206human GRCh38 chr2: 10,440,869-10,441,507 , GRCh37.p13 chr2: 10,580,995-10,581,633 ODC1
    nsv5451707copy number variation1nstd206human GRCh38 chr2: 10,441,930-10,442,011 , GRCh37.p13 chr2: 10,582,056-10,582,137 ODC1
    nsv5450378copy number variation1nstd206human GRCh38 chr2: 10,444,269-10,444,473 , GRCh37.p13 chr2: 10,584,395-10,584,599 ODC1
    nsv5440958copy number variation1nstd206human GRCh38 chr2: 10,445,049-10,445,154 , GRCh37.p13 chr2: 10,585,175-10,585,280 SNORA80B, ODC1
    nsv5438153copy number variation1nstd206human GRCh38 chr2: 10,444,647-10,444,929 , GRCh37.p13 chr2: 10,584,773-10,585,055 ODC1, SNORA80B
    nsv5437260copy number variation1nstd206human GRCh38 chr2: 10,443,836-10,444,092 , GRCh37.p13 chr2: 10,583,962-10,584,218 ODC1
    nsv5380046translocation1nstd200human GRCh38 chr2: 10,444,092-10,444,092 , GRCh38 chr2: 10,442,175-10,442,175 , GRCh37.p13 chr2: 10,582,301-10,582,301 , GRCh37.p13 chr2: 10,584,218-10,584,218 ODC1
    nsv5380041translocation1nstd200human GRCh38 chr2: 10,440,388-10,440,388 , GRCh38 chrX: 97,186,647-97,186,647 , GRCh37.p13 chrX: 96,441,646-96,441,646 , GRCh37.p13 chr2: 10,580,514-10,580,514 DIAPH2, ODC1
    nsv5357879translocation1nstd200human GRCh38 chr2: 10,448,120-10,448,120 , GRCh38 chr2: 10,445,266-10,445,266 , GRCh37.p13 chr2: 10,588,246-10,588,246 , GRCh37.p13 chr2: 10,585,392-10,585,392 ODC1, SNORA80B, 1 more genes
    nsv5357869translocation1nstd200human GRCh38 chr2: 10,443,836-10,443,836 , GRCh38 chr2: 10,444,092-10,444,092 , GRCh37.p13 chr2: 10,584,218-10,584,218 , GRCh37.p13 chr2: 10,583,962-10,583,962 ODC1
    nsv5357864translocation1nstd200human GRCh38 chr2: 10,443,229-10,443,229 , GRCh38 chr2: 10,442,176-10,442,176 , GRCh37.p13 chr2: 10,583,355-10,583,355 , GRCh37.p13 chr2: 10,582,302-10,582,302 ODC1
    nsv5357853translocation1nstd200human GRCh38 chr2: 10,441,507-10,441,507 , GRCh38 chr2: 10,440,869-10,440,869 , GRCh37.p13 chr2: 10,580,995-10,580,995 , GRCh37.p13 chr2: 10,581,633-10,581,633 ODC1
    nsv5345989translocation1nstd200human GRCh37 chr2: 10,588,246-10,588,246 , GRCh37 chr2: 10,584,772-10,584,772 , GRCh38.p12 chr2: 10,444,646-10,444,646 , GRCh38.p12 chr2: 10,448,120-10,448,120 ODC1, ODC1-DT
    nsv5344066translocation1nstd200human GRCh37 chr2: 10,585,055-10,585,055 , GRCh37 chr2: 10,584,773-10,584,773 , GRCh38.p12 chr2: 10,444,929-10,444,929 , GRCh38.p12 chr2: 10,444,647-10,444,647 ODC1, SNORA80B
    nsv5330708translocation1nstd200human GRCh37 chr2: 10,583,962-10,583,962 , GRCh37 chr2: 10,584,218-10,584,218 , GRCh38.p12 chr2: 10,444,092-10,444,092 , GRCh38.p12 chr2: 10,443,836-10,443,836 ODC1
    nsv5325352translocation1nstd204human GRCh38.p13 chr2: 10,445,266-10,445,266 , GRCh38.p13 chr2: 10,448,120-10,448,120 , GRCh37.p13 chr2: 10,585,392-10,585,392 , GRCh37.p13 chr2: 10,588,246-10,588,246 ODC1, SNORA80B, 1 more genes
    nsv5323492translocation1nstd204human GRCh37.p13 chr2: 10,584,772-10,584,772 , GRCh37.p13 chr2: 10,588,246-10,588,246 , GRCh38.p13 chr2: 10,444,646-10,444,646 , GRCh38.p13 chr2: 10,448,120-10,448,120 ODC1, ODC1-DT
    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