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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6950973copy number variation1nstd229human GRCh38 chr14: 20,013,858-20,436,718 , GRCh37.p13 chr14: 20,482,017-20,904,877 OR4L1, RNA5SP382, 25 more genes
    nsv6487981copy number variation1nstd223human GRCh38 chr14: 20,013,858-20,436,718 , GRCh37.p13 chr14: 20,482,017-20,904,877 RNA5SP382, OR4L1, 25 more genes
    nsv6482501copy number variation1nstd223human GRCh38 chr14: 20,054,901-20,072,600 , GRCh37.p13 chr14: 20,523,060-20,540,759 OR4L1
    nsv6476101copy number variation1nstd223human GRCh38 chr14: 20,052,001-20,070,900 , GRCh37.p13 chr14: 20,520,160-20,539,059 OR4L1
    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
    nsv6290645copy number variation1nstd102humanUncertain significance GRCh38 chr14: 20,013,858-20,436,718 , GRCh37.p13 chr14: 20,482,017-20,904,877 OR4T1P, OR11G1P, 25 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
    nsv6035638copy number variation1nstd212human GRCh38 chr14: 20,059,621-20,130,429 , GRCh37.p13 chr14: 20,527,780-20,598,588 OR4L1, OR4T1P, 2 more genes
    nsv5943393copy number variation1nstd209human GRCh38 chr14: 20,038,752-20,231,884 , GRCh37.p13 chr14: 20,506,911-20,700,043 PSMB7P1, OR11G2, 12 more genes
    nsv5933802copy number variation1nstd209human GRCh38 chr14: 20,052,562-20,072,589 , GRCh37.p13 chr14: 20,520,721-20,540,748 OR4L1
    nsv5860752copy number variation1nstd209human GRCh38 chr14: 20,052,578-20,071,526 , GRCh37.p13 chr14: 20,520,737-20,539,685 OR4L1
    nsv5494960copy number variation1nstd206human GRCh38 chr14: 20,052,562-20,072,591 , GRCh37.p13 chr14: 20,520,721-20,540,750 OR4L1
    nsv4994066copy number variation1nstd200human GRCh38 chr14: 20,052,562-20,072,591 , GRCh37.p13 chr14: 20,520,721-20,540,750 OR4L1
    nsv4994065copy number variation1nstd200human GRCh38 chr14: 20,038,750-20,129,722 , GRCh37.p13 chr14: 20,506,909-20,597,881 OR4L1, OR4K17, 3 more genes
    nsv4994063copy number variation1nstd200human GRCh38 chr14: 20,013,868-20,436,718 , GRCh37.p13 chr14: 20,482,027-20,904,877 OR4K17, OR4L1, 25 more genes
    nsv4848511copy number variation1nstd200human GRCh37 chr14: 20,520,721-20,540,750 , GRCh38.p12 chr14: 20,052,562-20,072,591 OR4L1
    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
    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
    nsv4668605copy number variation1nstd186human GRCh37 chr14: 20,524,593-20,528,461 , GRCh38.p12 chr14: 20,056,434-20,060,302 OR4L1
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