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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv6951080copy number variation1nstd229human GRCh38 chr14: 21,611,101-21,667,000 , GRCh37.p13 chr14: 22,079,258-22,135,214 OR4E2, TRAV1-1, 5 more genes
    nsv6945801copy number variation1nstd229human GRCh38 chr14: 21,634,102-21,645,975 , GRCh37.p13 chr14: 22,102,258-22,114,188 TRAV1-2, TRA, 2 more genes
    nsv6945800copy number variation1nstd229human GRCh38 chr14: 21,625,097-21,631,988 , GRCh37.p13 chr14: 22,093,250-22,100,141 TRA, OR10G2
    nsv6938799copy number variation1nstd229human GRCh38 chr14: 21,622,388-21,644,688 , GRCh37.p13 chr14: 22,090,541-22,112,908 TRAV1-2, TRA, 2 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
    nsv6576782inversion1nstd223human GRCh38 chr14: 21,632,334-21,632,829 , GRCh37.p13 chr14: 22,100,491-22,100,985 OR10G2, TRA
    nsv6486406copy number variation1nstd223human GRCh38 chr14: 21,538,051-22,772,225 , GRCh37.p13 chr14: 22,006,185-23,241,434 TRAJ54, TRAV9-1, 152 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
    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
    nsv5503475copy number variation1nstd206human GRCh38 chr14: 21,601,713-21,634,637 , GRCh37.p13 chr14: 22,069,863-22,102,793 OR10G2, TRAV1-1, 3 more genes
    nsv4728411copy number variation1nstd102humanUncertain significance GRCh37 chr14: 22,006,109-23,241,448 , GRCh38.p12 chr14: 21,537,975-22,772,239 OR4E2, TRAV10, 152 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
    nsv4628286copy number variation1nstd183human GRCh37 chr14: 22,071,202-22,104,306 , GRCh38.p12 chr14: 21,603,051-21,636,150 TRA, OR10G2, 3 more genes
    nsv4578270copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,717,093-24,027,220 , GRCh38.p12 chr14: 21,248,934-23,558,011 BCL2L2, CEBPE, 215 more genes
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