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 135

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7069781inversion1nstd229human GRCh38 chr16: 24,962,563-25,492,782 , GRCh37.p13 chr16: 24,973,884-25,504,103 CYCSP39, ARHGAP17, 13 more genes
    nsv7066307inversion1nstd229human GRCh38 chr16: 25,128,995-25,267,847 , GRCh37.p13 chr16: 25,140,316-25,279,168 AQP8, LCMT1, 3 more genes
    nsv7060826inversion1nstd229human GRCh38 chr16: 25,236,956-25,237,057 , GRCh37.p13 chr16: 25,248,277-25,248,378 ZKSCAN2
    nsv6993951copy number variation1nstd229human GRCh38 chr16: 25,250,080-25,253,778 , GRCh37.p13 chr16: 25,261,401-25,265,099 ZKSCAN2
    nsv6980888copy number variation1nstd229human GRCh38 chr16: 25,239,820-25,244,294 , GRCh37.p13 chr16: 25,251,141-25,255,615 ZKSCAN2
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6587463inversion1nstd223human GRCh38 chr16: 25,249,357-25,250,297 , GRCh37.p13 chr16: 25,260,678-25,261,618 ZKSCAN2
    nsv6579247inversion1nstd223human GRCh38 chr16: 25,249,374-25,249,997 , GRCh37.p13 chr16: 25,260,695-25,261,318 ZKSCAN2
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 LOC105371149, SLX1B, 166 more genes
    nsv6289847copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924 GAPDHP35, NSMCE1, 154 more genes
    nsv6250192mobile element insertion1nstd215human GRCh38 chr16: 25,248,263-25,248,263 , GRCh37.p13 chr16: 25,259,584-25,259,584 ZKSCAN2
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133267copy number variation1nstd213human GRCh37 chr16: 22,710,000-30,200,001 , GRCh38.p12 chr16: 22,698,679-30,188,680 ALDOA, AQP8, 169 more genes
    nsv6133266copy number variation1nstd213human GRCh37 chr16: 22,710,000-26,360,001 , GRCh38.p12 chr16: 22,698,679-26,348,680 AQP8, NDUFAB1, 54 more genes
    nsv5711392mobile element insertion1nstd211human GRCh38 chr16: 25,247,904-25,247,904 , GRCh37.p13 chr16: 25,259,225-25,259,225 ZKSCAN2
    nsv5423528mobile element insertion1nstd206human GRCh38 chr16: 25,247,904-25,247,955 , GRCh37.p13 chr16: 25,259,225-25,259,276 ZKSCAN2
    nsv5349578translocation1nstd200human GRCh38 chr16: 25,257,744-25,257,744 , GRCh38 chr16: 25,257,658-25,257,658 , GRCh37.p13 chr16: 25,268,979-25,268,979 , GRCh37.p13 chr16: 25,269,065-25,269,065 ZKSCAN2
    nsv5335951translocation1nstd200human GRCh37 chr16: 25,269,065-25,269,065 , GRCh37 chr16: 25,268,979-25,268,979 , GRCh38.p12 chr16: 25,257,744-25,257,744 , GRCh38.p12 chr16: 25,257,658-25,257,658 ZKSCAN2
    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