Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 115

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094423copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,242,819-25,103,366 , GRCh38.p12 chr14: 22,773,610-24,634,160 LINC00596, NGDN, 107 more genes
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv6947564copy number variation1nstd229human GRCh38 chr14: 22,948,954-22,956,711 , GRCh37.p13 chr14: 23,418,163-23,425,920 PRMT5-DT, HAUS4, 1 more genes
    nsv6582206inversion1nstd223human GRCh38 chr14: 22,948,563-22,949,170 , GRCh37.p13 chr14: 23,417,772-23,418,379 PRMT5-DT, HAUS4
    nsv6486760copy number variation1nstd223human GRCh38 chr14: 22,953,792-22,954,866 , GRCh37.p13 chr14: 23,423,001-23,424,075 PRMT5-DT, HAUS4
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6290276copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 20,925,965-23,649,548 , GRCh38.p12 chr14: 20,457,806-23,180,339 ANG, APEX1, 255 more genes
    nsv6142967copy number variation1nstd206human GRCh38 chr14: 22,949,713-22,955,713 , GRCh37.p13 chr14: 23,418,922-23,424,922 HAUS4, MIR4707, 1 more genes
    nsv6132862copy number variation1nstd213human GRCh37 chr14: 23,180,000-23,940,001 , GRCh38.p12 chr14: 22,710,791-23,470,792 BCL2L2, CEBPE, 47 more genes
    nsv6132775copy number variation1nstd213human GRCh37 chr14: 22,590,000-24,410,001 , GRCh38.p12 chr14: 22,122,042-23,940,792 BCL2L2, CEBPE, 167 more genes
    nsv6097813insertion1nstd212human GRCh38 chr14: 22,944,957-22,944,957 , GRCh37.p13 chr14: 23,414,166-23,414,166 PRMT5-DT, HAUS4
    nsv6033413copy number variation1nstd212human GRCh38 chr14: 22,944,811-22,944,966 , GRCh37.p13 chr14: 23,414,020-23,414,175 HAUS4, PRMT5-DT
    nsv5976914insertion1nstd209human GRCh38 chr14: 22,944,942-22,944,942 , GRCh37.p13 chr14: 23,414,151-23,414,151 PRMT5-DT, HAUS4
    nsv5662494insertion1nstd207human GRCh38 chr14: 22,944,954-22,944,954 , GRCh37.p13 chr14: 23,414,163-23,414,163 HAUS4, PRMT5-DT
    nsv5158403mobile element insertion1nstd203human GRCh38 chr14: 22,947,214-22,947,214 , GRCh37.p13 chr14: 23,416,423-23,416,423 HAUS4, PRMT5-DT
    nsv5154451mobile element insertion1nstd203human GRCh38 chr14: 22,947,216-22,947,216 , GRCh37.p13 chr14: 23,416,425-23,416,425 HAUS4, PRMT5-DT
    nsv5151324mobile element insertion1nstd203human GRCh38 chr14: 22,954,032-22,954,032 , GRCh37.p13 chr14: 23,423,241-23,423,241 PRMT5-DT, HAUS4
    nsv5147843mobile element insertion1nstd203human GRCh38 chr14: 22,947,218-22,947,218 , GRCh37.p13 chr14: 23,416,427-23,416,427 HAUS4, PRMT5-DT
    nsv5142572mobile element insertion1nstd203human GRCh38 chr14: 22,947,220-22,947,220 , GRCh37.p13 chr14: 23,416,429-23,416,429 HAUS4, PRMT5-DT
    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