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Items: 1 to 20 of 87

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141438copy number variation1nstd232human GRCh38.p12 chr14: 24,442,259-24,442,343 , GRCh37.p13 chr14: 24,911,465-24,911,549 KHNYN, SDR39U1, 1 more genes
    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
    nsv6957508copy number variation1nstd229human GRCh38 chr14: 24,399,886-24,442,195 , GRCh37.p13 chr14: 24,869,092-24,911,401 NYNRIN, KHNYN, 3 more genes
    nsv6952456copy number variation1nstd229human GRCh38 chr14: 24,438,280-24,441,977 , GRCh37.p13 chr14: 24,907,486-24,911,183 KHNYN, SDR39U1, 1 more genes
    nsv6943003copy number variation1nstd229human GRCh38 chr14: 24,434,118-24,435,314 , GRCh37.p13 chr14: 24,903,324-24,904,520 KHNYN
    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
    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
    nsv5697193mobile element insertion2nstd211human GRCh38 chr14: 24,422,913-24,422,913 , GRCh37.p13 chr14: 24,892,119-24,892,119 KHNYN
    nsv5508754copy number variation1nstd206human GRCh38 chr14: 24,435,710-24,435,874 , GRCh37.p13 chr14: 24,904,916-24,905,080 KHNYN
    nsv5426452mobile element insertion1nstd206human GRCh38 chr14: 24,422,913-24,422,964 , GRCh37.p13 chr14: 24,892,119-24,892,170 KHNYN
    nsv5189182mobile element insertion1nstd203human GRCh38 chr14: 24,427,498-24,427,513 , GRCh37.p13 chr14: 24,896,704-24,896,719 KHNYN, CBLN3
    nsv4994116copy number variation1nstd200human GRCh38 chr14: 24,434,118-24,435,315 , GRCh37.p13 chr14: 24,903,324-24,904,521 KHNYN
    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
    nsv4562444mobile element insertion1nstd166human GRCh37.p13 chr14: 24,896,705-24,896,705 , GRCh38.p12 chr14: 24,427,499-24,427,499 CBLN3, KHNYN
    nsv4513644mobile element insertion1nstd166human GRCh37.p13 chr14: 24,890,584-24,890,584 , GRCh38.p12 chr14: 24,421,378-24,421,378 KHNYN
    nsv4513559mobile element insertion1nstd166human GRCh37.p13 chr14: 24,892,104-24,892,104 , GRCh38.p12 chr14: 24,422,898-24,422,898 KHNYN
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