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 192

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv7041575inversion1nstd229human GRCh38 chr3: 161,218,843-161,225,038 , GRCh37.p13 chr3: 160,936,631-160,942,826 NMD3
    nsv7040545inversion1nstd229human GRCh38 chr3: 161,245,242-161,248,361 , GRCh37.p13 chr3: 160,963,030-160,966,149 NMD3
    nsv6737570copy number variation1nstd229human GRCh38 chr3: 161,185,201-161,222,600 , GRCh37.p13 chr3: 160,902,989-160,940,388 NMD3
    nsv6735435copy number variation1nstd229human GRCh38 chr3: 161,248,960-161,273,158 , GRCh37.p13 chr3: 160,966,748-160,990,946 NMD3, LOC105374187
    nsv6733860copy number variation1nstd229human GRCh38 chr3: 161,149,701-161,423,600 , GRCh37.p13 chr3: 160,867,489-161,141,388 LOC105374186, EEF1GP4, 6 more genes
    nsv6721950copy number variation1nstd229human GRCh38 chr3: 161,243,145-161,250,226 , GRCh37.p13 chr3: 160,960,933-160,968,014 NMD3
    nsv6720541copy number variation1nstd229human GRCh38 chr3: 160,927,633-161,461,576 , GRCh37.p13 chr3: 160,645,421-161,179,364 LOC112268450, PPM1L, 10 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6566374inversion1nstd223human GRCh38 chr3: 161,247,573-161,248,031 , GRCh37.p13 chr3: 160,965,361-160,965,819 NMD3
    nsv6557443inversion1nstd223human GRCh38 chr3: 161,245,242-161,248,361 , GRCh37.p13 chr3: 160,963,030-160,966,149 NMD3
    nsv6371487copy number variation1nstd223human GRCh38 chr3: 161,218,001-161,224,900 , GRCh37.p13 chr3: 160,935,789-160,942,688 NMD3
    nsv6369613copy number variation1nstd223human GRCh38 chr3: 161,245,241-161,250,249 , GRCh37.p13 chr3: 160,963,029-160,968,037 NMD3
    nsv6363419copy number variation1nstd223human GRCh38 chr3: 161,246,101-161,247,400 , GRCh37.p13 chr3: 160,963,889-160,965,188 NMD3
    nsv6297922copy number variation1nstd186human GRCh37 chr3: 160,962,883-160,965,589 , GRCh38.p12 chr3: 161,245,095-161,247,801 NMD3
    nsv6291134copy number variation1nstd102humanLikely benign GRCh37 chr3: 160,826,404-161,251,252 , GRCh38.p12 chr3: 161,108,616-161,533,464 LOC105374186, PSMC1P7, 9 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv6134676copy number variation1nstd213human GRCh37 chr3: 160,770,000-161,010,001 , GRCh38.p12 chr3: 161,052,212-161,292,213 B3GALNT1, NMD3, 4 more genes
    nsv5447423copy number variation1nstd206human GRCh38 chr3: 161,245,095-161,247,801 , GRCh37.p13 chr3: 160,962,883-160,965,589 NMD3
    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