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Items: 1 to 20 of 86

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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
    nsv7067018inversion1nstd229human GRCh38 chr14: 20,775,660-20,981,672 , GRCh37.p13 chr14: 21,243,819-21,449,831 LOC100507513, LOC100130571, 8 more genes
    nsv6957463copy number variation1nstd229human GRCh38 chr14: 20,753,501-20,801,400 , GRCh37.p13 chr14: 21,221,660-21,269,559 RNASE1, LOC107984671, 3 more genes
    nsv6949271copy number variation1nstd229human GRCh38 chr14: 20,782,509-20,782,716 , GRCh37.p13 chr14: 21,250,668-21,250,875 RNASE6, LOC107984671
    nsv6938293copy number variation1nstd229human GRCh38 chr14: 20,782,901-20,797,000 , GRCh37.p13 chr14: 21,251,060-21,265,159 LOC107984671, RNASE6, 1 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
    nsv6622260copy number variation1nstd224human GRCh37 chr14: 21,228,818-21,265,637 , GRCh38.p12 chr14: 20,760,659-20,797,478 RNASE6, EDDM3B, 2 more genes
    nsv6622259copy number variation1nstd224human GRCh37 chr14: 21,228,569-21,325,687 , GRCh38.p12 chr14: 20,760,410-20,857,528 RNASE6, EDDM3B, 3 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
    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
    nsv5502697copy number variation1nstd206human GRCh38 chr14: 20,778,060-20,779,629 , GRCh37.p13 chr14: 21,246,219-21,247,788 RNASE6, LOC107984671
    nsv4994069copy number variation1nstd200human GRCh38 chr14: 20,462,869-20,801,429 , GRCh37.p13 chr14: 20,931,028-21,269,588 , RNASE9, 34 more genes
    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
    nsv4629616copy number variation1nstd183human GRCh37 chr14: 20,800,765-21,257,878 , GRCh38.p12 chr14: 20,332,606-20,789,719 , EDDM3A, 43 more genes
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