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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
    nsv6946798copy number variation1nstd229human GRCh38 chr14: 20,555,975-20,753,534 , GRCh37.p13 chr14: 21,024,134-21,221,693 EDDM3A, RNASE9, 25 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
    nsv6578228inversion1nstd223human GRCh38 chr14: 20,589,395-20,589,861 , GRCh37.p13 chr14: 21,057,554-21,058,020 RNASE11, RNASE11-AS1, 1 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
    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
    nsv5495905copy number variation1nstd206human GRCh38 chr14: 20,585,239-20,585,330 , GRCh37.p13 chr14: 21,053,398-21,053,489 RNASE11
    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
    nsv4990708copy number variation1nstd200human GRCh38 chr14: 20,576,265-20,584,315 , GRCh37.p13 chr14: 21,044,424-21,052,474 RNASE11
    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
    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
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