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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147671insertion1nstd232human GRCh37.p13 chr14: 24,607,009-24,607,009 , GRCh38.p12 chr14: 24,137,800-24,137,800 , GRCh38.p12 chr14|NW_018654722.1: 438,778-438,778 PSME1, EMC9
    nsv7140544copy number variation1nstd232human GRCh37.p13 chr14: 24,607,607-24,607,680 , GRCh38.p12 chr14: 24,138,398-24,138,471 , GRCh38.p12 chr14|NW_018654722.1: 439,376-439,449 PSME1, EMC9
    nsv7139283copy number variation1nstd232human GRCh37.p13 chr14: 24,606,412-24,606,526 , GRCh38.p12 chr14: 24,137,203-24,137,317 , GRCh38.p12 chr14|NW_018654722.1: 438,181-438,295 PSME1, EMC9
    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
    nsv6940423copy number variation1nstd229human GRCh38 chr14: 24,127,601-24,140,800 , GRCh37.p13 chr14: 24,596,810-24,610,009 PSME1, EMC9, 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
    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
    nsv6143365copy number variation1nstd206human GRCh38 chr14: 24,135,713-24,141,713 , GRCh37.p13 chr14: 24,604,922-24,610,922 PSME2, EMC9, 2 more genes
    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
    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
    nsv4225607copy number variation1nstd166human GRCh37.p13 chr14: 24,605,000-24,617,000 , GRCh38.p12 chr14|NW_018654722.1: 436,769-448,769 , GRCh38.p12 chr14: 24,135,791-24,147,791 MIR7703, PSME1, 3 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
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