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Items: 1 to 20 of 127

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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
    nsv6952845copy number variation1nstd229human GRCh38 chr14: 24,080,557-24,080,940 , GRCh37.p13 chr14: 24,549,766-24,550,149 NRL
    nsv6942841copy number variation1nstd229human GRCh38 chr14: 24,084,445-24,085,635 , GRCh37.p13 chr14: 24,553,654-24,554,844 NRL
    nsv6941578copy number variation1nstd229human GRCh38 chr14: 24,093,094-24,096,095 , GRCh37.p13 chr14: 24,562,303-24,565,304 PCK2, NRL
    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
    nsv6482884copy number variation1nstd223human GRCh38 chr14: 24,097,704-24,099,071 , GRCh37.p13 chr14: 24,566,913-24,568,280 NRL, PCK2
    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
    nsv6143350copy number variation1nstd206human GRCh38 chr14: 24,105,713-24,171,713 , GRCh37.p13 chr14: 24,574,922-24,640,922 IRF9, PSME2, 9 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
    nsv5723154mobile element insertion2nstd211human GRCh38 chr14: 24,086,256-24,086,256 , GRCh37.p13 chr14: 24,555,465-24,555,465 NRL
    nsv5563027mobile element insertion1nstd206human GRCh38 chr14: 24,086,272-24,086,307 , GRCh37.p13 chr14: 24,555,481-24,555,516 NRL
    nsv5498875copy number variation1nstd206human GRCh38 chr14: 24,101,007-24,101,059 , GRCh37.p13 chr14: 24,570,216-24,570,268 NRL, PCK2
    nsv5263479copy number variation1nstd204human GRCh38.p13 chr14: 24,019,501-24,275,100 , GRCh37.p13 chr14: 24,488,710-24,744,306 , RABGGTA, 26 more genes
    nsv5155509mobile element insertion1nstd203human GRCh38 chr14: 24,102,227-24,102,242 , GRCh37.p13 chr14: 24,571,436-24,571,451 NRL, PCK2
    nsv5148703mobile element insertion1nstd203human GRCh38 chr14: 24,102,063-24,102,079 , GRCh37.p13 chr14: 24,571,272-24,571,288 PCK2, NRL
    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
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