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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941745copy number variation1nstd209human GRCh38 chr14: 21,042,351-21,042,407 , GRCh37.p13 chr14: 21,510,510-21,510,566 NDRG2, RNASE7
    nsv5938665copy number variation1nstd209human GRCh38 chr14: 21,067,972-21,068,297 , GRCh37.p13 chr14: 21,536,131-21,536,456 NDRG2, ARHGEF40
    nsv5594522copy number variation1nstd207human GRCh38 chr14: 21,067,972-21,068,297 , GRCh37.p13 chr14: 21,536,131-21,536,456 NDRG2, ARHGEF40
    nsv5512724copy number variation1nstd206human GRCh38 chr14: 21,063,773-21,064,083 , GRCh37.p13 chr14: 21,531,932-21,532,242 ARHGEF40, NDRG2
    nsv5510654copy number variation1nstd206human GRCh38 chr14: 21,043,472-21,043,678 , GRCh37.p13 chr14: 21,511,631-21,511,837 NDRG2, RNASE7
    nsv5501374copy number variation1nstd206human GRCh38 chr14: 21,042,353-21,042,408 , GRCh37.p13 chr14: 21,510,512-21,510,567 RNASE7, NDRG2
    nsv5494696copy number variation1nstd206human GRCh38 chr14: 21,067,985-21,068,298 , GRCh37.p13 chr14: 21,536,144-21,536,457 NDRG2, ARHGEF40
    nsv5385185mobile element deletion2nstd186human GRCh37 chr14: 21,536,144-21,536,457 , GRCh38.p12 chr14: 21,067,985-21,068,298 NDRG2, ARHGEF40
    nsv5203420mobile element deletion1nstd204human GRCh37.p13 chr14: 21,536,144-21,536,457 , GRCh38.p13 chr14: 21,067,985-21,068,298 ARHGEF40, NDRG2
    nsv5159129mobile element insertion1nstd203human GRCh38 chr14: 21,053,803-21,053,819 , GRCh37.p13 chr14: 21,521,962-21,521,978 NDRG2
    nsv4899963mobile element deletion1nstd200human GRCh38 chr14: 21,067,985-21,068,298 , GRCh37.p13 chr14: 21,536,144-21,536,457 ARHGEF40, NDRG2
    nsv4775328mobile element deletion1nstd200human GRCh37 chr14: 21,536,144-21,536,457 , GRCh38.p12 chr14: 21,067,985-21,068,298 NDRG2, ARHGEF40
    nsv4746242copy number variation1nstd199human GRCh37 chr14: 21,536,132-21,536,459 , GRCh38.p12 chr14: 21,067,973-21,068,300 NDRG2, ARHGEF40
    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
    nsv4711862copy number variation2nstd195human GRCh37 chr14: 21,536,131-21,536,132 , GRCh38.p12 chr14: 21,067,972-21,067,973 ARHGEF40, NDRG2
    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
    nsv4655237copy number variation2nstd186human GRCh37 chr14: 21,536,144-21,536,457 , GRCh38.p12 chr14: 21,067,985-21,068,298 ARHGEF40, NDRG2
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