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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941745copy number variation1nstd209human GRCh38 chr14: 21,042,351-21,042,407 , GRCh37.p13 chr14: 21,510,510-21,510,566 NDRG2, RNASE7
    nsv5510654copy number variation1nstd206human GRCh38 chr14: 21,043,472-21,043,678 , GRCh37.p13 chr14: 21,511,631-21,511,837 NDRG2, RNASE7
    nsv5501374copy number variation1nstd206human GRCh38 chr14: 21,042,353-21,042,408 , GRCh37.p13 chr14: 21,510,512-21,510,567 RNASE7, NDRG2
    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
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
    nsv4675977copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,159,605-22,252,320 , GRCh38.p12 chr14: 20,691,446-21,784,103 ANG, HNRNPC, 69 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
    nsv4654287copy number variation2nstd186human GRCh37 chr14: 21,510,512-21,510,567 , GRCh38.p12 chr14: 21,042,353-21,042,408 NDRG2, RNASE7
    nsv4629644copy number variation1nstd183human GRCh37 chr14: 21,496,021-21,671,277 , GRCh38.p12 chr14: 21,027,862-21,203,118 RNASE13, RNU6-252P, 15 more genes
    nsv4457241copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,490,055-21,962,265 , GRCh38.p12 chr14: 21,021,896-21,494,106 MIR6717, ZNF219, 29 more genes
    nsv4455746copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,424,506-21,589,630 , GRCh38.p12 chr14: 20,956,347-21,121,471 METTL17, LOC101929718, 17 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
    nsv4232081copy number variation1nstd166human GRCh37.p13 chr14: 21,510,512-21,510,567 , GRCh38.p12 chr14: 21,042,353-21,042,408 NDRG2, RNASE7
    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
    nsv3923482copy number variation1nstd102humanUncertain significance NCBI36 chr14: 20,576,991-20,988,060 , GRCh37.p13 chr14: 21,507,151-21,918,220 , GRCh38.p12 chr14: 21,038,992-21,450,061 UBA52P2, LOC112268132, 24 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
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