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Items: 1 to 20 of 105

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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
    nsv6939456copy number variation1nstd229human GRCh38 chr14: 20,236,540-20,251,527 , GRCh37.p13 chr14: 20,704,699-20,719,686 OR11H4
    nsv6938183copy number variation1nstd229human GRCh38 chr14: 20,243,506-20,243,689 , GRCh37.p13 chr14: 20,711,665-20,711,848 OR11H4
    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
    nsv6622257copy number variation3nstd224human GRCh37 chr14: 20,691,662-20,716,025 , GRCh38.p12 chr14: 20,223,503-20,247,866 OR11H4, OR11H7, 1 more genes
    nsv6493972copy number variation1nstd223human GRCh38 chr14: 20,211,746-20,276,405 , GRCh37.p13 chr14: 20,679,905-20,744,564 OR11H4, OR11H6, 1 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
    nsv5936132copy number variation1nstd209human GRCh38 chr14: 20,215,229-20,248,715 , GRCh37.p13 chr14: 20,683,388-20,716,874 OR11H6, OR11H7, 1 more genes
    nsv5866662copy number variation2nstd209human GRCh38 chr14: 20,237,192-20,242,484 , GRCh37.p13 chr14: 20,705,351-20,710,643 OR11H4
    nsv5862809copy number variation1nstd209human GRCh38 chr14: 20,238,691-20,248,000 , GRCh37.p13 chr14: 20,706,850-20,716,159 OR11H4
    nsv5858280copy number variation2nstd209human GRCh38 chr14: 20,237,291-20,241,076 , GRCh37.p13 chr14: 20,705,450-20,709,235 OR11H4
    nsv5855259copy number variation2nstd209human GRCh38 chr14: 20,237,191-20,243,498 , GRCh37.p13 chr14: 20,705,350-20,711,657 OR11H4
    nsv5512098copy number variation1nstd206human GRCh38 chr14: 20,211,743-20,276,391 , GRCh37.p13 chr14: 20,679,902-20,744,550 OR11H6, OR11H4, 1 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
    nsv4990688copy number variation1nstd200human GRCh38 chr14: 20,231,366-20,250,030 , GRCh37.p13 chr14: 20,699,525-20,718,189 OR11H4
    nsv4837094copy number variation1nstd200human GRCh37 chr14: 20,699,197-20,717,740 , GRCh38.p12 chr14: 20,231,038-20,249,581 OR11H4, OR11H7
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