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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067668inversion1nstd229human GRCh38 chr14: 20,196,129-20,199,434 , GRCh37.p13 chr14: 20,664,288-20,667,593 OR11G2
    nsv7065880inversion1nstd229human GRCh38 chr14: 20,195,389-20,204,069 , GRCh37.p13 chr14: 20,663,548-20,672,228 OR11G2
    nsv6954671copy number variation1nstd229human GRCh38 chr14: 20,186,239-20,200,498 , GRCh37.p13 chr14: 20,654,398-20,668,657 OR11G2
    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
    nsv6949316copy number variation1nstd229human GRCh38 chr14: 20,178,301-20,197,500 , GRCh37.p13 chr14: 20,646,460-20,665,659 OR11G2, OR11G1P, 1 more genes
    nsv6945954copy number variation1nstd229human GRCh38 chr14: 20,197,193-20,208,436 , GRCh37.p13 chr14: 20,665,352-20,676,595 OR11G2, OR11H5P
    nsv6491605copy number variation1nstd223human GRCh38 chr14: 20,109,001-20,201,200 , GRCh37.p13 chr14: 20,577,160-20,669,359 OR11P1P, OR11G1P, 5 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
    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
    nsv6314064copy number variation1nstd102humanUncertain significance GRCh37 chr14: 20,664,697-21,017,250 , GRCh38.p12 chr14: 20,196,538-20,549,091 LOC100422510, SNORA79B, 20 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
    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
    nsv5711582mobile element insertion1nstd211human GRCh38 chr14: 20,196,391-20,196,391 , GRCh37.p13 chr14: 20,664,550-20,664,550 OR11G2
    nsv5423320mobile element insertion1nstd206human GRCh38 chr14: 20,196,391-20,196,442 , GRCh37.p13 chr14: 20,664,550-20,664,601 OR11G2
    nsv4994067copy number variation1nstd200human GRCh38 chr14: 20,067,185-20,201,105 , GRCh37.p13 chr14: 20,535,344-20,669,264 OR4N5, OR11P1P, 7 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
    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
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