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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146130copy number variation1nstd232human GRCh37.p13 chr14: 23,374,220-23,374,300 , GRCh38.p12 chr14: 22,905,011-22,905,091 RBM23
    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
    nsv6949713copy number variation1nstd229human GRCh38 chr14: 22,902,628-22,903,463 , GRCh37.p13 chr14: 23,371,837-23,372,672 RBM23
    nsv6947245copy number variation1nstd229human GRCh38 chr14: 22,904,186-22,917,109 , GRCh37.p13 chr14: 23,373,395-23,386,318 RBM23
    nsv6938398copy number variation1nstd229human GRCh38 chr14: 22,895,130-22,910,644 , GRCh37.p13 chr14: 23,364,339-23,379,853 RBM23
    nsv6588938inversion1nstd223human GRCh38 chr14: 22,913,868-22,915,488 , GRCh37.p13 chr14: 23,383,077-23,384,697 RBM23
    nsv6588385inversion1nstd223human GRCh38 chr14: 22,906,815-22,909,079 , GRCh37.p13 chr14: 23,376,024-23,378,288 RBM23
    nsv6580468inversion1nstd223human GRCh38 chr14: 22,908,697-22,910,205 , GRCh37.p13 chr14: 23,377,906-23,379,414 RBM23
    nsv6484411copy number variation1nstd223human GRCh38 chr14: 22,918,194-22,921,612 , GRCh37.p13 chr14: 23,387,403-23,390,821 RBM23, PRMT5, 1 more genes
    nsv6479073copy number variation1nstd223human GRCh38 chr14: 22,894,456-22,895,099 , GRCh37.p13 chr14: 23,363,665-23,364,308 RBM23
    nsv6476938copy number variation1nstd223human GRCh38 chr14: 22,910,986-22,914,400 , GRCh37.p13 chr14: 23,380,195-23,383,609 RBM23
    nsv6476887copy number variation1nstd223human GRCh38 chr14: 22,897,495-22,901,159 , GRCh37.p13 chr14: 23,366,704-23,370,368 RBM23
    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
    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
    nsv6029192copy number variation1nstd212human GRCh38 chr14: 22,891,376-22,891,462 , GRCh37.p13 chr14: 23,360,585-23,360,671 RBM23
    nsv5941864copy number variation1nstd209human GRCh38 chr14: 22,894,713-22,895,017 , GRCh37.p13 chr14: 23,363,922-23,364,226 RBM23
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