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Items: 1 to 20 of 73

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5349021translocation1nstd200human GRCh38 chr14: 20,555,974-20,555,974 , GRCh38 chr14: 20,753,533-20,753,533 , GRCh37.p13 chr14: 21,024,133-21,024,133 , GRCh37.p13 chr14: 21,221,692-21,221,692 LOC107984671, RNASE9
    nsv4994069copy number variation1nstd200human GRCh38 chr14: 20,462,869-20,801,429 , GRCh37.p13 chr14: 20,931,028-21,269,588 , RNASE9, 34 more genes
    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
    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
    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
    nsv3920885copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,619,308-23,911,404 , NCBI36 chr14: 19,689,148-22,981,244 , GRCh38 chr14: 20,151,149-23,442,195 SLC39A2, APEX1, 294 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3918965copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,490,852-44,562,875 , GRCh38 chr14: 20,022,693-44,093,672 , NCBI36 chr14: 19,560,692-43,632,625 TRAJ13, LRP10, 589 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3917301copy number variation1nstd102humanPathogenic GRCh38 chr14: 19,755,249-22,741,281 , GRCh37 chr14: 20,223,408-23,210,490 , NCBI36 chr14: 19,293,248-22,280,330 RNASE8, TRAV6, 271 more genes
    nsv3916277copy number variation1nstd102humanPathogenic NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005 MIR208B, MRPL52, 600 more genes
    nsv3914336copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,475,357-21,613,255 , GRCh37 chr14: 20,943,516-22,081,409 , NCBI36 chr14: 20,013,356-21,151,249 TRP-TGG3-2, TRL-TAG2-1, 80 more genes
    nsv3913204copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-49,111,245 , GRCh38 chr14: 20,043,513-48,642,042 , NCBI36 chr14: 19,581,512-48,180,995 SMARCE1P3, LOC100421646, 635 more genes
    nsv3912710copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,000,611-38,984,415 , NCBI36 chr14: 19,538,610-38,523,370 , GRCh37 chr14: 20,468,770-39,453,619 UBE2NP1, MIR4307HG, 553 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
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