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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 more genes
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 more genes
    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
    nsv6314064copy number variation1nstd102humanUncertain significance GRCh37 chr14: 20,664,697-21,017,250 , GRCh38.p12 chr14: 20,196,538-20,549,091 LOC100422510, SNORA79B, 20 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
    nsv6132583copy number variation1nstd213human GRCh37 chr14: 20,420,000-22,590,001 , GRCh38.p12 chr14: 19,951,841-22,122,043 HNRNPC, PNP, 157 more genes
    nsv5271898copy number variation1nstd204human GRCh38.p13 chr14: 20,460,578-20,463,136 , GRCh37.p13 chr14: 20,928,737-20,931,295 PIP4P1
    nsv5146384mobile element insertion1nstd203human GRCh38 chr14: 20,458,832-20,458,840 , GRCh37.p13 chr14: 20,926,991-20,926,999 PIP4P1
    nsv4729394copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357 SETP1, OR11H5P, 99 more genes
    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
    nsv4629616copy number variation1nstd183human GRCh37 chr14: 20,800,765-21,257,878 , GRCh38.p12 chr14: 20,332,606-20,789,719 , EDDM3A, 43 more genes
    nsv4623091copy number variation1nstd183human GRCh37 chr14: 20,923,705-20,925,048 , GRCh38.p12 chr14: 20,455,546-20,456,889 PIP4P1, APEX1
    nsv4621556copy number variation1nstd183human GRCh37 chr14: 20,922,500-20,924,889 , GRCh38.p12 chr14: 20,454,341-20,456,730 OSGEP, APEX1, 1 more genes
    nsv4501975mobile element insertion1nstd166human GRCh37.p13 chr14: 20,926,991-20,926,991 , GRCh38.p12 chr14: 20,458,832-20,458,832 PIP4P1
    nsv4455321copy number variation1nstd102humanUncertain significance GRCh37 chr14: 20,511,672-21,174,548 , GRCh38.p12 chr14: 20,043,513-20,706,389 PARP2, TRL-AAG2-3, 53 more genes
    nsv4349901copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881 TRAV4, UNGP2, 458 more genes
    nsv4220744copy number variation1nstd166human GRCh37.p13 chr14: 20,922,000-20,934,000 , GRCh38.p12 chr14: 20,453,841-20,465,841 APEX1, PIP4P1, 1 more genes
    nsv3924761copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,127,290-21,376,436 , NCBI36 chr14: 19,665,289-20,914,435 , GRCh37 chr14: 20,595,449-21,844,595 ANG, TMEM253, 87 more genes
    nsv3922265copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 19,950,586-24,557,166 , GRCh37 chr14: 20,880,746-25,487,326 , GRCh38 chr14: 20,412,587-25,018,120 ANG, APEX1, 346 more genes
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