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 987

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125658copy number variation1nstd186human GRCh37 chr19: 9,015,192-9,017,985 , GRCh38.p12 chr19: 8,904,516-8,907,309 MUC16
    nsv5976438insertion1nstd209human GRCh38 chr19: 8,931,343-8,931,343 , GRCh37.p13 chr19: 9,042,019-9,042,019 MUC16
    nsv5968843insertion1nstd209human GRCh38 chr19: 8,896,564-8,896,564 , GRCh37.p13 chr19: 9,007,240-9,007,240 MUC16
    nsv5968354insertion1nstd209human GRCh38 chr19: 8,982,068-8,982,068 , GRCh37.p13 chr19: 9,092,744-9,092,744 MUC16
    nsv5946824copy number variation1nstd209human GRCh38 chr19: 8,884,374-8,884,520 , GRCh37.p13 chr19: 8,995,050-8,995,196 MUC16
    nsv5936250copy number variation1nstd209human GRCh38 chr19: 8,931,524-9,173,686 , GRCh37.p13 chr19: 9,042,200-9,284,362 ZNF317, OR7G1, 8 more genes
    nsv5932260copy number variation1nstd209human GRCh38 chr19: 8,932,063-8,932,120 , GRCh37.p13 chr19: 9,042,739-9,042,796 MUC16
    nsv5931485copy number variation1nstd209human GRCh38 chr19: 8,888,616-8,891,724 , GRCh37.p13 chr19: 8,999,292-9,002,400 MUC16
    nsv5928158copy number variation1nstd209human GRCh38 chr19: 8,904,485-8,907,299 , GRCh37.p13 chr19: 9,015,161-9,017,975 MUC16
    nsv5881197copy number variation1nstd209human GRCh38 chr19: 8,889,018-8,891,681 , GRCh37.p13 chr19: 8,999,694-9,002,357 MUC16
    nsv5870156copy number variation1nstd209human GRCh38 chr19: 8,888,418-8,890,881 , GRCh37.p13 chr19: 8,999,094-9,001,557 MUC16
    nsv5869592copy number variation2nstd209human GRCh38 chr19: 8,904,466-8,907,270 , GRCh37.p13 chr19: 9,015,142-9,017,946 MUC16
    nsv5719560mobile element insertion1nstd211human GRCh38 chr19: 8,883,908-8,883,908 , GRCh37.p13 chr19: 8,994,584-8,994,584 MUC16
    nsv5662360insertion1nstd207human GRCh38 chr19: 8,896,151-8,896,151 , GRCh37.p13 chr19: 9,006,827-9,006,827 MUC16
    nsv5659354insertion1nstd207human GRCh38 chr19: 8,895,814-8,895,814 , GRCh37.p13 chr19: 9,006,490-9,006,490 MUC16
    nsv5657818insertion1nstd207human GRCh38 chr19: 8,931,343-8,931,343 , GRCh37.p13 chr19: 9,042,019-9,042,019 MUC16
    nsv5657593insertion1nstd207human GRCh38 chr19: 8,897,441-8,897,441 , GRCh37.p13 chr19: 9,008,117-9,008,117 MUC16
    nsv5654810insertion1nstd207human GRCh38 chr19: 8,898,649-8,898,649 , GRCh37.p13 chr19: 9,009,325-9,009,325 MUC16
    nsv5647022insertion1nstd207human GRCh38 chr19: 8,904,228-8,904,228 , GRCh37.p13 chr19: 9,014,904-9,014,904 MUC16
    nsv5604036copy number variation1nstd207human GRCh38 chr19: 8,884,374-8,884,520 , GRCh37.p13 chr19: 8,995,050-8,995,196 MUC16
    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