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Items: 1 to 20 of 80

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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
    nsv6948275copy number variation1nstd229human GRCh38 chr14: 24,121,518-24,122,970 , GRCh37.p13 chr14: 24,590,727-24,592,179 DCAF11
    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
    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
    nsv5494014copy number variation1nstd206human GRCh38 chr14: 24,122,332-24,124,984 , GRCh37.p13 chr14: 24,591,541-24,594,193 DCAF11
    nsv5349041translocation1nstd200human GRCh38 chr14: 24,122,539-24,122,539 , GRCh38 chr14: 24,122,481-24,122,481 , GRCh37.p13 chr14: 24,591,748-24,591,748 , GRCh37.p13 chr14: 24,591,690-24,591,690 DCAF11
    nsv5339846translocation1nstd200human GRCh37 chr14: 24,591,748-24,591,748 , GRCh37 chr14: 24,591,690-24,591,690 , GRCh38.p12 chr14|NW_018654722.1: 423,459-423,459 , GRCh38.p12 chr14: 24,122,539-24,122,539 , GRCh38.p12 chr14: 24,122,481-24,122,481 , GRCh38.p12 chr14|NW_018654722.1: 423,517-423,517 DCAF11
    nsv5327667translocation1nstd204human GRCh38.p13 chr14: 24,122,481-24,122,481 , GRCh38.p13 chr14: 24,122,539-24,122,539 , GRCh37.p13 chr14: 24,591,748-24,591,748 , GRCh37.p13 chr14: 24,591,690-24,591,690 DCAF11
    nsv5278790copy number variation1nstd204human GRCh38.p13 chr14: 24,122,132-24,124,417 , GRCh37.p13 chr14: 24,591,341-24,593,626 DCAF11
    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
    nsv5154712mobile element insertion1nstd203human GRCh38 chr14: 24,120,556-24,120,571 , GRCh37.p13 chr14: 24,589,765-24,589,780 DCAF11
    nsv4830431copy number variation1nstd200human GRCh37 chr14: 24,591,034-24,591,375 , GRCh38.p12 chr14|NW_018654722.1: 422,803-423,144 , GRCh38.p12 chr14: 24,121,825-24,122,166 DCAF11
    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
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