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Items: 1 to 20 of 72

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094423copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,242,819-25,103,366 , GRCh38.p12 chr14: 22,773,610-24,634,160 LINC00596, NGDN, 107 more genes
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv7070619inversion1nstd229human GRCh38 chr14: 23,713,943-24,501,695 , GRCh37.p13 chr14: 24,183,152-24,970,901 TSSK4, RIPK3, 48 more genes
    nsv6955724copy number variation1nstd229human GRCh38 chr14: 24,292,884-24,388,476 , GRCh37.p13 chr14: 24,762,090-24,857,682 NFATC4, LTB4R, 6 more genes
    nsv6941402copy number variation1nstd229human GRCh38 chr14: 24,059,301-24,305,100 , GRCh37.p13 chr14: 24,528,510-24,774,306 PSME2, CIDEB, 27 more genes
    nsv6481955copy number variation1nstd223human GRCh38 chr14: 24,292,884-24,388,472 , GRCh37.p13 chr14: 24,762,090-24,857,678 LTB4R, NFATC4, 6 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
    nsv6132776copy number variation1nstd213human GRCh37 chr14: 24,490,000-28,000,001 , GRCh38.p12 chr14: 24,020,791-27,530,795 CMA1, LTB4R, 65 more genes
    nsv5502990copy number variation1nstd206human GRCh38 chr14: 24,274,165-24,318,169 , GRCh37.p13 chr14: 24,743,371-24,787,375 , LTB4R, 5 more genes
    nsv5312811copy number variation1nstd204human GRCh38.p13 chr14: 24,274,162-24,318,178 , GRCh37.p13 chr14: 24,743,368-24,787,384 , LTB4R, 5 more genes
    nsv5261015copy number variation1nstd204human GRCh38.p13 chr14: 24,306,876-24,309,375 , GRCh37.p13 chr14: 24,776,082-24,778,581 NOP9, CIDEB, 1 more genes
    nsv4990889copy number variation1nstd200human GRCh38 chr14: 24,304,745-24,304,832 , GRCh37.p13 chr14: 24,773,951-24,774,038 NOP9, CIDEB
    nsv4838093copy number variation1nstd200human GRCh37 chr14: 24,743,371-24,787,375 , GRCh38.p12 chr14: 24,274,165-24,318,169 , GRCh38.p12 chr14|NW_018654722.1: 575,143-619,147 , LTB4R, 5 more genes
    nsv4832490copy number variation1nstd200human GRCh37 chr14: 24,773,951-24,774,038 , GRCh38.p12 chr14: 24,304,745-24,304,832 , GRCh38.p12 chr14|NW_018654722.1: 605,723-605,810 NOP9, CIDEB
    nsv4728842copy number variation1nstd102humanUncertain significance GRCh37 chr14: 24,163,771-24,818,728 , GRCh38.p12 chr14: 23,694,562-24,347,428 , GRCh38.p12 chr14|NW_018654722.1: 1-650,500 FITM1, CIDEB, 44 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
    nsv4624494copy number variation1nstd183human GRCh37 chr14: 24,743,364-24,787,375 , GRCh38.p12 chr14: 24,274,158-24,318,169 , GRCh38.p12 chr14|NW_018654722.1: 575,136-619,147 , LTB4R, 5 more genes
    nsv4349901copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881 TRAV4, UNGP2, 458 more genes
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