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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147250insertion1nstd232human GRCh37.p13 chr14: 50,085,858-50,085,858 , GRCh38.p12 chr14: 49,619,140-49,619,140 MGAT2, RPL36AL
    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
    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
    nsv6482187copy number variation1nstd223human GRCh38 chr14: 49,622,701-49,623,600 , GRCh37.p13 chr14: 50,089,419-50,090,318 MGAT2, DNAAF2
    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
    nsv6315095delins1nstd102humanUncertain significance GRCh38 chr14: 49,622,450-49,622,564 , GRCh37 chr14: 50,089,168-50,089,282 MGAT2
    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
    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
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv4633184copy number variation1nstd183human GRCh37 chr14: 50,087,241-50,100,117 , GRCh38.p12 chr14: 49,620,523-49,633,399 DNAAF2, MGAT2, 1 more genes
    nsv4629838copy number variation1nstd183human GRCh37 chr14: 49,986,935-50,930,979 , GRCh38.p12 chr14: 49,520,217-50,464,261 , RNU6-189P, 37 more genes
    nsv4623203copy number variation1nstd183human GRCh37 chr14: 49,893,688-50,942,527 , GRCh38.p12 chr14: 49,426,970-50,475,809 , LOC105378179, 38 more genes
    nsv4218063copy number variation1nstd166human GRCh37.p13 chr14: 50,082,340-50,116,458 , GRCh38.p12 chr14: 49,615,622-49,649,740 , DNAAF2, 3 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
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