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 224

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7076161inversion1nstd229human GRCh38 chr16: 67,897,916-67,902,980 , GRCh37.p13 chr16: 67,931,819-67,936,883 PSKH1
    nsv7075094inversion1nstd229human GRCh38 chr16: 67,913,190-69,541,641 , GRCh37.p13 chr16: 67,947,093-69,575,544 PSMB10, COG8, 52 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv7062477inversion1nstd229human GRCh38 chr16: 67,899,815-67,902,980 , GRCh37.p13 chr16: 67,933,718-67,936,883 PSKH1
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6995421copy number variation1nstd229human GRCh38 chr16: 67,891,780-67,905,720 , GRCh37.p13 chr16: 67,925,683-67,939,623 PSKH1
    nsv6994907copy number variation1nstd229human GRCh38 chr16: 67,923,841-67,926,854 , GRCh37.p13 chr16: 67,957,744-67,960,757 PSKH1
    nsv6987867copy number variation1nstd229human GRCh38 chr16: 67,764,668-68,219,679 , GRCh37.p13 chr16: 67,798,571-68,253,582 DDX28, NUTF2, 19 more genes
    nsv6987567copy number variation1nstd229human GRCh38 chr16: 67,914,107-67,917,905 , GRCh37.p13 chr16: 67,948,010-67,951,808 PSKH1
    nsv6983664copy number variation1nstd229human GRCh38 chr16: 67,899,601-67,905,100 , GRCh37.p13 chr16: 67,933,504-67,939,003 PSKH1
    nsv6979614copy number variation1nstd229human GRCh38 chr16: 67,899,101-67,905,700 , GRCh37.p13 chr16: 67,933,004-67,939,603 PSKH1
    nsv6623489copy number variation1nstd224human GRCh37 chr16: 67,943,050-68,068,627 , GRCh38.p12 chr16: 67,909,147-68,034,724 DPEP2NB, PSKH1, 10 more genes
    nsv6508491copy number variation1nstd223human GRCh38 chr16: 67,895,696-67,906,186 , GRCh37.p13 chr16: 67,929,599-67,940,089 PSKH1
    nsv6507530copy number variation1nstd223human GRCh38 chr16: 67,905,010-67,905,695 , GRCh37.p13 chr16: 67,938,913-67,939,598 PSKH1
    nsv6503627copy number variation1nstd223human GRCh38 chr16: 67,899,628-67,905,045 , GRCh37.p13 chr16: 67,933,531-67,938,948 PSKH1
    nsv6503352copy number variation1nstd223human GRCh38 chr16: 67,897,758-67,898,746 , GRCh37.p13 chr16: 67,931,661-67,932,649 PSKH1
    nsv6499578copy number variation1nstd223human GRCh38 chr16: 67,893,001-67,893,700 , GRCh37.p13 chr16: 67,926,904-67,927,603 PSKH1
    nsv6498985copy number variation1nstd223human GRCh38 chr16: 67,890,434-67,891,504 , GRCh37.p13 chr16: 67,924,337-67,925,407 PSKH1
    nsv6496410copy number variation1nstd223human GRCh38 chr16: 67,906,801-67,911,100 , GRCh37.p13 chr16: 67,940,704-67,945,003 PSKH1
    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