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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6592169inversion1nstd223human GRCh38 chr14: 49,610,602-49,611,455 , GRCh37.p13 chr14: 50,077,320-50,078,173 LRR1
    nsv6491503copy number variation1nstd223human GRCh38 chr14: 49,599,601-49,600,200 , GRCh37.p13 chr14: 50,066,319-50,066,918 LRR1, RHOQP1
    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
    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
    nsv5500143copy number variation1nstd206human GRCh38 chr14: 49,588,888-49,597,671 , GRCh37.p13 chr14: 50,055,606-50,064,389 LRR1, RPS29
    nsv5159196mobile element insertion1nstd203human GRCh38 chr14: 49,608,423-49,608,496 , GRCh37.p13 chr14: 50,075,141-50,075,214 LRR1
    nsv5155212mobile element insertion1nstd203human GRCh38 chr14: 49,609,217-49,609,227 , GRCh37.p13 chr14: 50,075,935-50,075,945 LRR1
    nsv5155085mobile element insertion1nstd203human GRCh38 chr14: 49,609,239-49,609,289 , GRCh37.p13 chr14: 50,075,957-50,076,007 LRR1
    nsv5154691mobile element insertion1nstd203human GRCh38 chr14: 49,610,311-49,610,315 , GRCh37.p13 chr14: 50,077,029-50,077,033 LRR1
    nsv5152288mobile element insertion1nstd203human GRCh38 chr14: 49,608,406-49,608,447 , GRCh37.p13 chr14: 50,075,124-50,075,165 LRR1
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