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 311

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939393copy number variation1nstd209human GRCh38 chr14: 104,097,211-104,097,266 , GRCh37.p13 chr14: 104,563,548-104,563,603 ASPG
    nsv5927698copy number variation1nstd209human GRCh38 chr14: 104,087,894-104,093,763 , GRCh37.p13 chr14: 104,554,231-104,560,100 ASPG
    nsv5859746copy number variation1nstd209human GRCh38 chr14: 104,087,867-104,093,543 , GRCh37.p13 chr14: 104,554,204-104,559,880 ASPG
    nsv5851421copy number variation1nstd209human GRCh38 chr14: 104,090,417-104,092,743 , GRCh37.p13 chr14: 104,556,754-104,559,080 ASPG
    nsv5662413insertion1nstd207human GRCh38 chr14: 104,098,127-104,098,127 , GRCh37.p13 chr14: 104,564,464-104,564,464 ASPG
    nsv5659201insertion1nstd207human GRCh38 chr14: 104,098,112-104,098,112 , GRCh37.p13 chr14: 104,564,449-104,564,449 ASPG
    nsv5653915insertion1nstd207human GRCh38 chr14: 104,085,483-104,085,483 , GRCh37.p13 chr14: 104,551,820-104,551,820 ASPG
    nsv5645549insertion1nstd207human GRCh38 chr14: 104,097,878-104,097,878 , GRCh37.p13 chr14: 104,564,215-104,564,215 ASPG
    nsv5601092copy number variation1nstd207human GRCh38 chr14: 104,097,809-104,097,860 , GRCh37.p13 chr14: 104,564,146-104,564,197 ASPG
    nsv5509508copy number variation1nstd206human GRCh38 chr14: 104,087,874-104,093,786 , GRCh37.p13 chr14: 104,554,211-104,560,123 ASPG
    nsv5504618copy number variation1nstd206human GRCh38 chr14: 104,066,681-104,089,743 , GRCh37.p13 chr14: 104,533,018-104,556,080 ASPG
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5379910translocation1nstd200human GRCh38 chr14: 104,129,128-104,129,128 , GRCh38 chr14: 104,084,052-104,084,052 , GRCh37.p13 chr14: 104,595,465-104,595,465 , GRCh37.p13 chr14: 104,550,389-104,550,389 ASPG
    nsv5345200translocation1nstd200human GRCh37 chr14: 104,550,389-104,550,389 , GRCh37 chr14: 104,595,465-104,595,465 , GRCh38.p12 chr14: 104,084,052-104,084,052 , GRCh38.p12 chr14: 104,129,128-104,129,128 ASPG
    nsv5325299translocation1nstd204human GRCh38.p13 chr14: 104,084,052-104,084,052 , GRCh38.p13 chr14: 104,129,128-104,129,128 , GRCh37.p13 chr14: 104,550,389-104,550,389 , GRCh37.p13 chr14: 104,595,465-104,595,465 ASPG
    nsv5274806copy number variation1nstd204human GRCh38.p13 chr14: 104,084,079-104,088,216 , GRCh37.p13 chr14: 104,550,416-104,554,553 ASPG
    nsv5153113mobile element insertion1nstd203human GRCh38 chr14: 104,108,225-104,108,235 , GRCh37.p13 chr14: 104,574,562-104,574,572 ASPG
    nsv5005032copy number variation1nstd200human GRCh38 chr14: 104,058,547-104,336,906 , GRCh37.p13 chr14: 104,524,884-104,803,243 ASPG, MIR203B, 4 more genes
    nsv5005031copy number variation1nstd200human GRCh38 chr14: 103,944,079-104,113,007 , GRCh37.p13 chr14: 104,410,416-104,579,344 ASPG, RN7SL634P, 1 more genes
    nsv4991555copy number variation1nstd200human GRCh38 chr14: 104,105,926-104,110,407 , GRCh37.p13 chr14: 104,572,263-104,576,744 ASPG
    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