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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094423copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,242,819-25,103,366 , GRCh38.p12 chr14: 22,773,610-24,634,160 LINC00596, NGDN, 107 more genes
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv7070619inversion1nstd229human GRCh38 chr14: 23,713,943-24,501,695 , GRCh37.p13 chr14: 24,183,152-24,970,901 TSSK4, RIPK3, 48 more genes
    nsv6941402copy number variation1nstd229human GRCh38 chr14: 24,059,301-24,305,100 , GRCh37.p13 chr14: 24,528,510-24,774,306 PSME2, CIDEB, 27 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
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6189975copy number variation1nstd214human GRCh38 chr14: 24,171,158-24,171,213 , GRCh37.p13 chr14: 24,640,367-24,640,422 REC8
    nsv6143350copy number variation1nstd206human GRCh38 chr14: 24,105,713-24,171,713 , GRCh37.p13 chr14: 24,574,922-24,640,922 IRF9, PSME2, 9 more genes
    nsv6132776copy number variation1nstd213human GRCh37 chr14: 24,490,000-28,000,001 , GRCh38.p12 chr14: 24,020,791-27,530,795 CMA1, LTB4R, 65 more genes
    nsv5263479copy number variation1nstd204human GRCh38.p13 chr14: 24,019,501-24,275,100 , GRCh37.p13 chr14: 24,488,710-24,744,306 , RABGGTA, 26 more genes
    nsv5207273mobile element deletion1nstd204human GRCh38.p13 chr14: 24,175,715-24,176,003 , GRCh37.p13 chr14: 24,644,924-24,645,212 REC8
    nsv4775333mobile element deletion1nstd200human GRCh37 chr14: 24,644,933-24,645,208 , GRCh38.p12 chr14: 24,175,724-24,175,999 , GRCh38.p12 chr14|NW_018654722.1: 476,702-476,977 REC8
    nsv4728842copy number variation1nstd102humanUncertain significance GRCh37 chr14: 24,163,771-24,818,728 , GRCh38.p12 chr14: 23,694,562-24,347,428 , GRCh38.p12 chr14|NW_018654722.1: 1-650,500 FITM1, CIDEB, 44 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
    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
    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
    nsv3919655copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,453,274-25,843,700 , GRCh38 chr14: 23,984,065-25,374,494 , NCBI36 chr14: 23,523,114-24,913,540 NFATC4, LTB4R, 50 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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