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Items: 1 to 20 of 79

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5309985copy number variation1nstd204human GRCh37.p13 chr14: 27,346,529-27,429,831 , GRCh38.p13 chr14: 26,877,323-26,960,625 UNGP2, MIR4307, 2 more genes
    nsv5266616copy number variation1nstd204human GRCh38.p13 chr14: 26,919,436-26,960,372 , GRCh37.p13 chr14: 27,388,642-27,429,578 UNGP2, LOC105370419
    nsv5262545copy number variation1nstd204human GRCh38.p13 chr14: 26,877,301-26,960,600 , GRCh37.p13 chr14: 27,346,507-27,429,806 MIR4307, MIR4307HG, 2 more genes
    nsv4990985copy number variation1nstd200human GRCh38 chr14: 26,910,674-26,965,401 , GRCh37.p13 chr14: 27,379,880-27,434,607 MIR4307HG, LOC105370419, 1 more genes
    nsv4990984copy number variation1nstd200human GRCh38 chr14: 26,877,326-26,960,624 , GRCh37.p13 chr14: 27,346,532-27,429,830 MIR4307HG, UNGP2, 2 more genes
    nsv4990981copy number variation1nstd200human GRCh38 chr14: 26,830,462-26,927,134 , GRCh37.p13 chr14: 27,299,668-27,396,340 MIR4307, MIR4307HG, 1 more genes
    nsv4847028copy number variation1nstd200human GRCh37 chr14: 27,346,532-27,429,830 , GRCh38.p12 chr14: 26,877,326-26,960,624 LOC105370419, MIR4307, 2 more genes
    nsv4839324copy number variation1nstd200human GRCh37 chr14: 27,379,880-27,434,607 , GRCh38.p12 chr14: 26,910,674-26,965,401 LOC105370419, MIR4307HG, 1 more genes
    nsv4729530copy number variation1nstd102humanPathogenic GRCh37 chr14: 25,172,628-30,285,023 , GRCh38.p12 chr14: 24,703,422-29,815,817 LINC02281, RNU6-864P, 42 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
    nsv4529455copy number variation1nstd166human GRCh37.p13 chr14: 26,335,999-27,430,000 , GRCh38.p12 chr14: 25,866,793-26,960,794 MIR4307, LOC105370419, 8 more genes
    nsv4373451copy number variation1nstd173human GRCh37 chr14: 26,562,813-27,424,344 , GRCh38.p12 chr14: 26,093,607-26,955,138 MIR4307, LOC105370418, 8 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
    nsv4217491copy number variation1nstd166human GRCh37.p13 chr14: 27,359,218-27,808,722 , GRCh38.p12 chr14: 26,890,012-27,339,516 UNGP2, RPS27AP4, 6 more genes
    nsv3966846copy number variation1nstd168human GRCh38 chr14: 26,923,445-26,960,051 , GRCh37.p13 chr14: 27,392,651-27,429,257 LOC105370419, UNGP2
    nsv3924893copy number variation1nstd102humanUncertain significance NCBI36 chr14: 26,444,800-27,017,977 , GRCh37 chr14: 27,374,960-27,948,137 , GRCh38 chr14: 26,905,754-27,478,931 UNGP2, RPS27AP4, 6 more genes
    nsv3924892copy number variation1nstd102humanLikely benign GRCh37 chr14: 27,210,934-27,791,995 , NCBI36 chr14: 26,280,774-26,861,835 , GRCh38 chr14: 26,741,728-27,322,789 LOC105370421, MIR3171HG, 9 more genes
    nsv3922163copy number variation1nstd102humanPathogenic NCBI36 chr14: 26,243,854-32,957,356 , GRCh37.p13 chr14: 27,174,014-33,887,605 , GRCh38.p12 chr14: 26,704,808-33,418,399 LINC02293, ARHGAP5, 77 more genes
    nsv3921872copy number variation1nstd102humanBenign NCBI36 chr14: 26,138,826-27,249,760 , GRCh38 chr14: 26,599,780-27,710,714 , GRCh37 chr14: 27,068,986-28,179,920 LOC105370421, RPS27AP4, 11 more genes
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