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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098984copy number variation1nstd102humanLikely pathogenic GRCh38 chr4: 110,650,730-112,833,790 , GRCh37.p13 chr4: 111,571,886-113,754,946 ANK2, LARP7, 36 more genes
    nsv7057794inversion1nstd229human GRCh38 chr4: 112,107,668-113,032,310 , GRCh37.p13 chr4: 113,028,824-113,953,466 AP1AR, RPS12P8, 28 more genes
    nsv7054431inversion1nstd229human GRCh38 chr4: 108,267,754-117,667,771 , GRCh37.p13 chr4: 109,188,910-118,588,926 , MIR297, 128 more genes
    nsv7043065inversion1nstd229human GRCh38 chr4: 112,692,974-112,872,266 , GRCh37.p13 chr4: 113,614,130-113,793,422 ANK2, RPL32P13, 4 more genes
    nsv7040232inversion1nstd229human GRCh38 chr4: 112,768,066-112,864,697 , GRCh37.p13 chr4: 113,689,222-113,785,853 LOC100422627, LOC100131158, 2 more genes
    nsv6756407copy number variation1nstd229human GRCh38 chr4: 112,827,365-112,831,195 , GRCh37.p13 chr4: 113,748,521-113,752,351 LOC100422627, ANK2
    nsv6754372copy number variation1nstd229human GRCh38 chr4: 112,787,382-113,004,716 , GRCh37.p13 chr4: 113,708,538-113,925,872 LOC100131158, LOC102723896, 3 more genes
    nsv6749284copy number variation1nstd229human GRCh38 chr4: 112,452,598-112,840,857 , GRCh37.p13 chr4: 113,373,754-113,762,013 H3P14, RPL32P13, 18 more genes
    nsv6738275copy number variation1nstd229human GRCh38 chr4: 112,652,701-112,940,200 , GRCh37.p13 chr4: 113,573,857-113,861,356 RPL32P13, LOC100131158, 7 more genes
    nsv6629339copy number variation1nstd224human GRCh37 chr4: 113,311,741-113,784,482 , GRCh38.p12 chr4: 112,390,585-112,863,326 LARP7, NEUROG2, 19 more genes
    nsv6572140inversion1nstd223human GRCh38 chr4: 108,267,752-117,667,773 , GRCh37.p13 chr4: 109,188,908-118,588,928 , RPS26P25, 128 more genes
    nsv6556222inversion1nstd223human GRCh38 chr4: 108,711,905-115,978,756 , GRCh37.p13 chr4: 109,633,061-116,899,912 , MIR577, 98 more genes
    nsv6315356copy number variation1nstd102humanUncertain significance GRCh37 chr4: 112,481,911-113,756,889 , GRCh38.p12 chr4: 111,560,755-112,835,733 RPL36AP19, RPL7AP30, 31 more genes
    nsv6314915copy number variation1nstd102humanUncertain significance GRCh38 chr4: 112,631,945-112,883,056 , GRCh37.p13 chr4: 113,553,101-113,804,212 RPL32P13, ZGRF1, 14 more genes
    nsv6313895copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 112,849,108-115,434,557 , GRCh38.p12 chr4: 111,927,952-114,513,401 ANK2, CAMK2D, 45 more genes
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6135274copy number variation1nstd213human GRCh37 chr4: 112,840,000-113,770,001 , GRCh38.p12 chr4: 111,918,844-112,848,845 ANK2, LARP7, 29 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
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