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Items: 1 to 20 of 95

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074841inversion1nstd229human GRCh38 chr14: 36,720,867-38,925,376 , GRCh37.p13 chr14: 37,190,072-39,394,580 SSTR1, RNU6-1277P, 18 more genes
    nsv7063114inversion1nstd229human GRCh38 chr14: 38,103,582-38,838,586 , GRCh37.p13 chr14: 38,572,787-39,307,790 LOC112268136, CLEC14A, 4 more genes
    nsv6957901copy number variation1nstd229human GRCh38 chr14: 38,175,369-38,279,175 , GRCh37.p13 chr14: 38,644,574-38,748,380 LOC112268136, SSTR1, 1 more genes
    nsv6948068copy number variation1nstd229human GRCh38 chr14: 38,070,280-38,323,384 , GRCh37.p13 chr14: 38,539,485-38,792,588 LOC112268136, SSTR1, 1 more genes
    nsv6944659copy number variation1nstd229human GRCh38 chr14: 38,254,301-38,256,900 , GRCh37.p13 chr14: 38,723,506-38,726,105 LOC112268136, CLEC14A
    nsv6944005copy number variation1nstd229human GRCh38 chr14: 38,251,721-38,285,806 , GRCh37.p13 chr14: 38,720,926-38,755,010 LOC112268136, CLEC14A
    nsv6637388copy number variation1nstd102humanUncertain significance GRCh37 chr14: 37,486,532-39,796,638 , GRCh38.p12 chr14: 37,017,327-39,327,434 GEMIN2, FOXA1, 30 more genes
    nsv6484639copy number variation1nstd223human GRCh38 chr14: 38,254,501-38,256,500 , GRCh37.p13 chr14: 38,723,706-38,725,705 LOC112268136, CLEC14A
    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
    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
    nsv6313916copy number variation1nstd102humanPathogenic GRCh37 chr14: 36,862,276-41,597,549 , GRCh38.p12 chr14: 36,393,071-41,128,344 LOC105370462, LOC105370459, 55 more genes
    nsv6132591copy number variation1nstd213human GRCh37 chr14: 38,680,000-40,710,001 , GRCh38.p12 chr14: 38,210,795-40,240,797 PNN, SSTR1, 26 more genes
    nsv6106211inversion1nstd212human GRCh38 chr14: 35,414,234-38,834,329 , GRCh37.p13 chr14: 35,883,440-39,303,533 , FOXA1, 49 more genes
    nsv5381757copy number variation1nstd102humanPathogenic GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164 RPLP0P3, KRT18P6, 131 more genes
    nsv5303224copy number variation1nstd204human GRCh38.p13 chr14: 37,973,892-39,705,239 , GRCh37.p13 chr14: 38,443,097-40,174,443 RPL7AP2, LOC112268136, 25 more genes
    nsv5278802copy number variation1nstd204human GRCh38.p13 chr14: 38,101,201-39,697,400 , GRCh37.p13 chr14: 38,570,406-40,166,604 LOC100313942, PNN, 24 more genes
    nsv4994217copy number variation1nstd200human GRCh38 chr14: 37,973,902-39,705,237 , GRCh37.p13 chr14: 38,443,107-40,174,441 LOC100422334, TRAPPC6B, 25 more genes
    nsv4844239copy number variation1nstd200human GRCh37 chr14: 38,443,107-40,174,441 , GRCh38.p12 chr14: 37,973,902-39,705,237 LOC105370460, LOC102723516, 25 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
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