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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094431copy number variation1nstd102humanUncertain significance GRCh37 chr14: 50,050,385-50,053,064 , GRCh38.p12 chr14: 49,583,667-49,586,346 RPS29, RN7SL1
    nsv7077973inversion1nstd229human GRCh38 chr14: 49,579,076-49,581,135 , GRCh37.p13 chr14: 50,045,794-50,047,853 RPS29
    nsv7076302inversion1nstd229human GRCh38 chr14: 46,512,743-51,785,975 , GRCh37.p13 chr14: 46,981,946-52,252,693 LOC100420098, MAP4K5, 82 more genes
    nsv7063700inversion1nstd229human GRCh38 chr14: 48,591,726-55,698,685 , GRCh37.p13 chr14: 49,060,929-56,165,403 ZFP64P1, LINC02331, 132 more genes
    nsv6948114copy number variation1nstd229human GRCh38 chr14: 49,590,801-49,603,100 , GRCh37.p13 chr14: 50,057,519-50,069,818 LRR1, RHOQP1, 1 more genes
    nsv6946633copy number variation1nstd229human GRCh38 chr14: 49,579,846-49,580,195 , GRCh37.p13 chr14: 50,046,564-50,046,913 RPS29
    nsv6944352copy number variation1nstd229human GRCh38 chr14: 49,536,501-49,712,100 , GRCh37.p13 chr14: 50,003,219-50,178,818 RN7SL1, RPS29, 12 more genes
    nsv6938412copy number variation1nstd229human GRCh38 chr14: 46,367,427-52,468,480 , GRCh37.p13 chr14: 46,836,630-52,935,198 RNU6-297P, RN7SL452P, 95 more genes
    nsv6622741copy number variation1nstd224human GRCh37 chr14: 50,007,787-50,049,252 , GRCh38.p12 chr14: 49,541,069-49,582,534 RPL32P29, RNA5SP384, 2 more genes
    nsv6590857inversion1nstd223human GRCh38 chr14: 49,592,375-49,592,844 , GRCh37.p13 chr14: 50,059,093-50,059,562 RPS29
    nsv6588574inversion1nstd223human GRCh38 chr14: 49,590,248-49,590,810 , GRCh37.p13 chr14: 50,056,966-50,057,528 RPS29
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 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
    nsv6314025copy number variation1nstd102humanUncertain significance GRCh37 chr14: 45,827,312-50,529,931 , GRCh38.p12 chr14: 45,358,109-50,063,213 RPL18P1, RPL10L, 52 more genes
    nsv6309547copy number variation1nstd102humanUncertain significance GRCh37 chr14: 50,050,385-50,118,115 , GRCh38.p12 chr14: 49,583,667-49,651,397 RHOQP1, RN7SL1, 6 more genes
    nsv6189849copy number variation1nstd214human GRCh38 chr14: 49,584,085-49,584,154 , GRCh37.p13 chr14: 50,050,803-50,050,872 RPS29
    nsv6132928copy number variation1nstd213human GRCh37 chr14: 48,670,000-50,170,001 , GRCh38.p12 chr14: 48,200,797-49,703,283 POLE2, RPL36AL, 19 more genes
    nsv6132786copy number variation1nstd213human GRCh37 chr14: 49,920,000-50,150,001 , GRCh38.p12 chr14: 49,453,282-49,683,283 DNAAF2, LRR1, 11 more genes
    nsv6028687copy number variation1nstd212human GRCh38 chr14: 49,590,364-49,590,419 , GRCh37.p13 chr14: 50,057,082-50,057,137 RPS29
    nsv5935670copy number variation1nstd209human GRCh38 chr14: 49,588,663-49,591,446 , GRCh37.p13 chr14: 50,055,381-50,058,164 , RPS29
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