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Items: 1 to 20 of 115

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    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
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