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 158

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941864copy number variation1nstd209human GRCh38 chr14: 22,894,713-22,895,017 , GRCh37.p13 chr14: 23,363,922-23,364,226 RBM23
    nsv5650793insertion1nstd207human GRCh38 chr14: 22,910,151-22,910,151 , GRCh37.p13 chr14: 23,379,360-23,379,360 RBM23
    nsv5504350copy number variation1nstd206human GRCh38 chr14: 22,902,628-22,903,463 , GRCh37.p13 chr14: 23,371,837-23,372,672 RBM23
    nsv5307183copy number variation1nstd204human GRCh38.p13 chr14: 22,902,625-22,903,472 , GRCh37.p13 chr14: 23,371,834-23,372,681 RBM23
    nsv5260854copy number variation1nstd204human GRCh38.p13 chr14: 22,897,992-22,898,991 , GRCh37.p13 chr14: 23,367,201-23,368,200 RBM23
    nsv5152867mobile element insertion1nstd203human GRCh38 chr14: 22,913,756-22,913,769 , GRCh37.p13 chr14: 23,382,965-23,382,978 RBM23
    nsv5143111mobile element insertion1nstd203human GRCh38 chr14: 22,905,767-22,905,781 , GRCh37.p13 chr14: 23,374,976-23,374,990 RBM23
    nsv4990840copy number variation1nstd200human GRCh38 chr14: 22,914,280-22,918,344 , GRCh37.p13 chr14: 23,383,489-23,387,553 PRMT5-AS1, RBM23
    nsv4990839copy number variation1nstd200human GRCh38 chr14: 22,910,979-22,914,402 , GRCh37.p13 chr14: 23,380,188-23,383,611 RBM23
    nsv4990838copy number variation1nstd200human GRCh38 chr14: 22,902,628-22,903,463 , GRCh37.p13 chr14: 23,371,837-23,372,672 RBM23
    nsv4849399copy number variation1nstd200human GRCh37 chr14: 23,383,517-23,387,526 , GRCh38.p12 chr14: 22,914,308-22,918,317 PRMT5-AS1, RBM23
    nsv4843088copy number variation1nstd200human GRCh37 chr14: 23,380,172-23,383,609 , GRCh38.p12 chr14: 22,910,963-22,914,400 RBM23
    nsv4746177copy number variation1nstd199human GRCh37 chr14: 23,360,579-23,360,657 , GRCh38.p12 chr14: 22,891,370-22,891,448 RBM23
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4667079copy number variation1nstd186human GRCh37 chr14: 23,371,837-23,372,687 , GRCh38.p12 chr14: 22,902,628-22,903,478 RBM23
    nsv4632069copy number variation1nstd183human GRCh37 chr14: 23,371,837-23,372,687 , GRCh38.p12 chr14: 22,902,628-22,903,478 RBM23
    nsv4622845copy number variation1nstd183human GRCh37 chr14: 23,374,378-23,380,835 , GRCh38.p12 chr14: 22,905,169-22,911,626 RBM23
    nsv4578270copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,717,093-24,027,220 , GRCh38.p12 chr14: 21,248,934-23,558,011 BCL2L2, CEBPE, 215 more genes
    nsv4575375mobile element insertion1nstd166human GRCh37.p13 chr14: 23,369,516-23,369,516 , GRCh38.p12 chr14: 22,900,307-22,900,307 RBM23
    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