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 286

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129726insertion1nstd186human GRCh37 chr16: 57,027,043-57,027,086 , GRCh38.p12 chr16: 56,993,131-56,993,174 NLRC5
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5972724insertion1nstd209human GRCh38 chr16: 56,993,123-56,993,123 , GRCh37.p13 chr16: 57,027,035-57,027,035 NLRC5
    nsv5968899insertion1nstd209human GRCh38 chr16: 57,030,438-57,030,438 , GRCh37.p13 chr16: 57,064,350-57,064,350 NLRC5
    nsv5943278copy number variation1nstd209human GRCh38 chr16: 57,030,438-57,030,617 , GRCh37.p13 chr16: 57,064,350-57,064,529 NLRC5
    nsv5885276copy number variation1nstd209human GRCh38 chr16: 57,007,055-57,010,804 , GRCh37.p13 chr16: 57,040,967-57,044,716 NLRC5
    nsv5704398mobile element insertion1nstd211human GRCh38 chr16: 57,013,879-57,013,879 , GRCh37.p13 chr16: 57,047,791-57,047,791 CFAP69P1, NLRC5
    nsv5701535mobile element insertion1nstd211human GRCh38 chr16: 57,075,047-57,075,047 , GRCh37.p13 chr16: 57,108,959-57,108,959 NLRC5
    nsv5697100mobile element insertion1nstd211human GRCh38 chr16: 57,052,081-57,052,081 , GRCh37.p13 chr16: 57,085,993-57,085,993 NLRC5
    nsv5663561insertion1nstd207human GRCh38 chr16: 56,993,088-56,993,088 , GRCh37.p13 chr16: 57,027,000-57,027,000 NLRC5
    nsv5652656insertion1nstd207human GRCh38 chr16: 57,070,926-57,070,926 , GRCh37.p13 chr16: 57,104,838-57,104,838 NLRC5
    nsv5648360insertion1nstd207human GRCh38 chr16: 57,071,659-57,071,659 , GRCh37.p13 chr16: 57,105,571-57,105,571 NLRC5
    nsv5596274copy number variation1nstd207human GRCh38 chr16: 57,070,897-57,071,044 , GRCh37.p13 chr16: 57,104,809-57,104,956 NLRC5
    nsv5594242copy number variation1nstd207human GRCh38 chr16: 57,070,948-57,071,020 , GRCh37.p13 chr16: 57,104,860-57,104,932 NLRC5
    nsv5547196insertion1nstd206human GRCh38 chr16: 56,993,131-56,993,174 , GRCh37.p13 chr16: 57,027,043-57,027,086 NLRC5
    nsv5533857copy number variation1nstd206human GRCh38 chr16: 57,011,453-57,014,410 , GRCh37.p13 chr16: 57,045,365-57,048,322 NLRC5, CFAP69P1
    nsv5531930copy number variation1nstd206human GRCh38 chr16: 57,006,946-57,010,884 , GRCh37.p13 chr16: 57,040,858-57,044,796 NLRC5
    nsv5417668mobile element insertion1nstd206human GRCh38 chr16: 57,052,081-57,052,085 , GRCh37.p13 chr16: 57,085,993-57,085,997 NLRC5
    nsv5415225mobile element insertion1nstd206human GRCh38 chr16: 57,013,879-57,013,930 , GRCh37.p13 chr16: 57,047,791-57,047,842 CFAP69P1, NLRC5
    nsv5358217translocation1nstd200human GRCh38 chr16: 57,051,971-57,051,971 , GRCh38 chr16: 57,052,036-57,052,036 , GRCh37.p13 chr16: 57,085,948-57,085,948 , GRCh37.p13 chr16: 57,085,883-57,085,883 NLRC5
    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