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Items: 1 to 20 of 73

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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
    nsv6941845copy number variation1nstd229human GRCh38 chr14: 21,665,996-21,670,421 , GRCh37.p13 chr14: 22,134,210-22,138,636 OR4E1, OR4E2, 1 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
    nsv6582528inversion1nstd223human GRCh38 chr14: 21,662,315-21,663,265 , GRCh37.p13 chr14: 22,130,528-22,131,478 TRA, OR4E2
    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
    nsv5717601mobile element insertion1nstd211human GRCh38 chr14: 21,663,185-21,663,185 , GRCh37.p13 chr14: 22,131,398-22,131,398 TRA, OR4E2
    nsv5562060mobile element insertion1nstd206human GRCh38 chr14: 21,663,185-21,663,236 , GRCh37.p13 chr14: 22,131,398-22,131,449 TRA, OR4E2
    nsv5420568mobile element insertion1nstd206human GRCh38 chr14: 21,663,036-21,663,087 , GRCh37.p13 chr14: 22,131,249-22,131,300 OR4E2, TRA
    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
    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
    nsv4455618copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,678,344-22,299,981 , GRCh38.p12 chr14: 21,210,185-21,831,825 TRAV3, RBBP4P5, 36 more genes
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