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 377

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965866copy number variation1nstd209human GRCh38 chr22: 46,687,275-46,687,337 , GRCh37.p13 chr22: 47,083,172-47,083,234 CERK
    nsv5602945copy number variation1nstd207human GRCh38 chr22: 46,687,275-46,687,337 , GRCh37.p13 chr22: 47,083,172-47,083,234 CERK
    nsv5550695copy number variation1nstd206human GRCh38 chr22: 46,718,547-46,726,921 , GRCh37.p13 chr22: 47,114,444-47,122,818 CERK
    nsv5538993copy number variation1nstd206human GRCh38 chr22: 46,723,465-46,724,803 , GRCh37.p13 chr22: 47,119,362-47,120,700 CERK
    nsv5535335copy number variation1nstd206human GRCh38 chr22: 46,692,224-46,692,702 , GRCh37.p13 chr22: 47,088,121-47,088,599 CERK
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 WBP2NL, RN7SKP80, 210 more genes
    nsv5327234copy number variation1nstd204human GRCh38.p13 chr22: 46,718,543-46,726,930 , GRCh37.p13 chr22: 47,114,440-47,122,827 CERK
    nsv5292974copy number variation1nstd204human GRCh38.p13 chr22: 46,719,352-46,726,901 , GRCh37.p13 chr22: 47,115,249-47,122,798 CERK
    nsv5209520mobile element deletion1nstd204human GRCh38.p13 chr22: 46,712,830-46,713,064 , GRCh37.p13 chr22: 47,108,727-47,108,961 CERK
    nsv5162748mobile element insertion1nstd203human GRCh38 chr22: 46,710,840-46,710,854 , GRCh37.p13 chr22: 47,106,737-47,106,751 CERK
    nsv5040967copy number variation1nstd200human GRCh38 chr22: 46,731,686-46,741,107 , GRCh37.p13 chr22: 47,127,583-47,137,004 CERK, LOC105373077
    nsv5033551copy number variation1nstd200human GRCh38 chr22: 46,586,124-46,702,806 , GRCh37.p13 chr22: 46,982,021-47,098,703 GRAMD4, CERK
    nsv5033377copy number variation1nstd200human GRCh38 chr22: 46,718,547-46,726,921 , GRCh37.p13 chr22: 47,114,444-47,122,818 CERK
    nsv5030363copy number variation1nstd200human GRCh38 chr22: 46,724,277-46,730,848 , GRCh37.p13 chr22: 47,120,174-47,126,745 CERK
    nsv4893160mobile element deletion1nstd200human GRCh38 chr22: 46,712,839-46,713,056 , GRCh37.p13 chr22: 47,108,736-47,108,953 CERK
    nsv4889019copy number variation1nstd200human GRCh37 chr22: 47,120,174-47,126,745 , GRCh38.p12 chr22: 46,724,277-46,730,848 CERK
    nsv4885164copy number variation1nstd200human GRCh37 chr22: 47,114,444-47,122,818 , GRCh38.p12 chr22: 46,718,547-46,726,921 CERK
    nsv4881657copy number variation1nstd200human GRCh37 chr22: 46,982,021-47,098,703 , GRCh38.p12 chr22: 46,586,124-46,702,806 CERK, GRAMD4
    nsv4873185copy number variation1nstd200human GRCh37 chr22: 47,088,087-47,088,609 , GRCh38.p12 chr22: 46,692,190-46,692,712 CERK
    nsv4777737mobile element deletion1nstd200human GRCh37 chr22: 47,108,736-47,108,953 , GRCh38.p12 chr22: 46,712,839-46,713,056 CERK
    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