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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 more genes
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv6948481copy number variation1nstd229human GRCh38 chr14: 20,997,461-20,997,838 , GRCh37.p13 chr14: 21,465,620-21,465,997 SLC39A2, LOC101929718, 1 more genes
    nsv6942045copy number variation1nstd229human GRCh38 chr14: 20,978,967-21,087,818 , GRCh37.p13 chr14: 21,447,126-21,555,977 MIR6717, LOC100130571, 10 more genes
    nsv6939521copy number variation1nstd229human GRCh38 chr14: 20,980,779-20,988,914 , GRCh37.p13 chr14: 21,448,938-21,457,073 LOC100130571, METTL17
    nsv6637326copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,349,608-21,618,292 , GRCh38.p12 chr14: 20,881,449-21,150,133 RNASE13, ARHGEF40, 21 more genes
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 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
    nsv6314121copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,451,544-21,962,317 , GRCh38.p12 chr14: 20,983,385-21,494,158 ZNF219, EIF4EBP1P1, 33 more genes
    nsv6290276copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 20,925,965-23,649,548 , GRCh38.p12 chr14: 20,457,806-23,180,339 ANG, APEX1, 255 more genes
    nsv6132583copy number variation1nstd213human GRCh37 chr14: 20,420,000-22,590,001 , GRCh38.p12 chr14: 19,951,841-22,122,043 HNRNPC, PNP, 157 more genes
    nsv5148186mobile element insertion1nstd203human GRCh38 chr14: 20,990,646-20,990,662 , GRCh37.p13 chr14: 21,458,805-21,458,821 METTL17
    nsv4729394copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357 SETP1, OR11H5P, 99 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
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
    nsv4675977copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,159,605-22,252,320 , GRCh38.p12 chr14: 20,691,446-21,784,103 ANG, HNRNPC, 69 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
    nsv4624187copy number variation1nstd183human GRCh37 chr14: 21,458,401-21,458,689 , GRCh38.p12 chr14: 20,990,242-20,990,530 METTL17
    nsv4455746copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,424,506-21,589,630 , GRCh38.p12 chr14: 20,956,347-21,121,471 METTL17, LOC101929718, 17 more genes
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