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 155

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148136copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,367,259-101,508,462 , GRCh38.p12 chr14: 99,900,922-101,042,125 SNORD113-5, SNORD114-27, 99 more genes
    nsv6975296copy number variation1nstd229human GRCh38 chr14: 100,953,886-100,962,414 , GRCh37.p13 chr14: 101,420,223-101,428,751 SNORD114-6, MEG8, 4 more genes
    nsv6962348copy number variation1nstd229human GRCh38 chr14: 100,955,912-100,963,742 , GRCh37.p13 chr14: 101,422,249-101,430,079 SNORD114-6, SNORD114-7, 3 more genes
    nsv6958859copy number variation1nstd229human GRCh38 chr14: 100,868,127-101,331,726 , GRCh37.p13 chr14: 101,334,464-101,798,063 MIR136, MIR329-2, 97 more genes
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6497121copy number variation1nstd223human GRCh38 chr14: 100,955,601-100,956,700 , GRCh37.p13 chr14: 101,421,938-101,423,037 SNORD114-5, SNORD114-6, 1 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6291768copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186 CCDC85C, MEG3, 206 more genes
    nsv6132885copy number variation1nstd213human GRCh37 chr14: 99,590,000-101,630,001 , GRCh38.p12 chr14: 99,123,663-101,163,664 DLK1, MEG8, 135 more genes
    nsv6083019insertion1nstd212human GRCh38 chr14: 100,957,556-100,957,556 , GRCh37.p13 chr14: 101,423,893-101,423,893 MEG8, SNORD114-6
    nsv6027823copy number variation1nstd212human GRCh38 chr14: 100,957,275-100,957,558 , GRCh37.p13 chr14: 101,423,612-101,423,895 MEG8, SNORD114-6
    nsv5654553insertion1nstd207human GRCh38 chr14: 100,957,286-100,957,286 , GRCh37.p13 chr14: 101,423,623-101,423,623 MEG8, SNORD114-6
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4618949copy number variation1nstd183human GRCh37 chr14: 101,372,908-101,884,282 , GRCh38.p12 chr14: 100,906,571-101,417,945 , LOC100128373, 90 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4455156copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229 IGHG4, IGHV3-57, 464 more genes
    nsv4445738insertion1nstd175human GRCh37 chr14: 101,423,612-101,423,612 , GRCh38.p12 chr14: 100,957,275-100,957,275 MEG8, SNORD114-6
    nsv4413532copy number variation1nstd174human GRCh37 chr14: 101,372,741-101,967,655 , GRCh38.p12 chr14: 100,906,404-101,501,318 , MIR369, 92 more genes
    nsv4349898copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 99,737,888-101,847,855 , GRCh38.p12 chr14: 99,271,551-101,381,518 EML1, WARS1, 136 more genes
    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