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Items: 1 to 20 of 123

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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
    nsv6950588copy number variation1nstd229human GRCh38 chr14: 24,334,807-24,370,379 , GRCh37.p13 chr14: 24,804,013-24,839,585 NFATC4, RIPK3, 1 more genes
    nsv6944211copy number variation1nstd229human GRCh38 chr14: 24,331,001-24,335,500 , GRCh37.p13 chr14: 24,800,207-24,804,706 RIPK3, ADCY4
    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
    nsv6258624mobile element insertion1nstd215human GRCh38 chr14: 24,325,222-24,325,222 , GRCh37.p13 chr14: 24,794,428-24,794,428 ADCY4
    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
    nsv6129462insertion1nstd186human GRCh37 chr14: 24,794,428-24,794,428 , GRCh38.p12 chr14: 24,325,222-24,325,222 , GRCh38.p12 chr14|NW_018654722.1: 626,200-626,200 ADCY4
    nsv6082512insertion1nstd212human GRCh38 chr14: 24,325,222-24,325,222 , GRCh37.p13 chr14: 24,794,428-24,794,428 ADCY4
    nsv6030750copy number variation1nstd212human GRCh38 chr14: 24,326,164-24,326,361 , GRCh37.p13 chr14: 24,795,370-24,795,567 ADCY4
    nsv5968471insertion1nstd209human GRCh38 chr14: 24,325,222-24,325,222 , GRCh37.p13 chr14: 24,794,428-24,794,428 ADCY4
    nsv5695117mobile element insertion2nstd211human GRCh38 chr14: 24,325,222-24,325,222 , GRCh37.p13 chr14: 24,794,428-24,794,428 ADCY4
    nsv5647036insertion1nstd207human GRCh38 chr14: 24,325,222-24,325,222 , GRCh37.p13 chr14: 24,794,428-24,794,428 ADCY4
    nsv5535960insertion1nstd206human GRCh38 chr14: 24,325,222-24,325,222 , GRCh37.p13 chr14: 24,794,428-24,794,428 ADCY4
    nsv5507526copy number variation1nstd206human GRCh38 chr14: 24,326,164-24,326,361 , GRCh37.p13 chr14: 24,795,370-24,795,567 ADCY4
    nsv5502990copy number variation1nstd206human GRCh38 chr14: 24,274,165-24,318,169 , GRCh37.p13 chr14: 24,743,371-24,787,375 , LTB4R, 5 more genes
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