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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5513563copy number variation1nstd206human GRCh38 chr14: 20,603,030-20,604,575 , GRCh37.p13 chr14: 21,071,189-21,072,734 RNASE11-AS1
    nsv5510652copy number variation1nstd206human GRCh38 chr14: 20,604,514-20,604,855 , GRCh37.p13 chr14: 21,072,673-21,073,014 RNASE11-AS1
    nsv5353890translocation1nstd200human GRCh38 chr1: 151,599,044-151,599,044 , GRCh38 chr14: 20,596,673-20,596,673 , GRCh37.p13 chr14: 21,064,832-21,064,832 , GRCh37.p13 chr1: 151,571,520-151,571,520 RNASE11-AS1
    nsv4994069copy number variation1nstd200human GRCh38 chr14: 20,462,869-20,801,429 , GRCh37.p13 chr14: 20,931,028-21,269,588 , RNASE9, 34 more genes
    nsv4990710copy number variation1nstd200human GRCh38 chr14: 20,590,279-20,591,645 , GRCh37.p13 chr14: 21,058,438-21,059,804 RNASE11, RNASE12, 1 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
    nsv4529570copy number variation1nstd166human GRCh37.p13 chr14: 21,056,999-21,249,000 , GRCh38.p12 chr14: 20,588,840-20,780,841 , TRY-GTA5-4, 27 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
    nsv4345126sequence alteration1nstd166human GRCh37.p13 chr14: 21,057,419-21,062,588 , GRCh38.p12 chr14: 20,589,260-20,594,429 RNASE11, RNASE11-AS1, 1 more genes
    nsv4219349copy number variation1nstd166human GRCh37.p13 chr14: 21,069,211-21,070,454 , GRCh38.p12 chr14: 20,601,052-20,602,295 RNASE11-AS1
    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
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