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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148228copy number variation1nstd102humanPathogenic GRCh38 chr19: 35,811,865-35,846,292 , GRCh37.p13 chr19: 36,302,767-36,337,194 PRODH2, NPHS1
    nsv7099006copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 36,322,665-36,330,138 , GRCh38.p12 chr19: 35,831,763-35,839,236 NPHS1
    nsv7098965copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 36,337,097-36,340,451 , GRCh38.p12 chr19: 35,846,195-35,849,549 NPHS1
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7095276copy number variation1nstd102humanPathogenic GRCh37 chr19: 36,338,828-36,339,610 , GRCh38.p12 chr19: 35,847,926-35,848,708 NPHS1
    nsv7093062copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 36,337,097-36,341,265 , GRCh38.p12 chr19: 35,846,195-35,850,363 NPHS1, KIRREL2
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7066069inversion1nstd229human GRCh38 chr19: 35,840,401-35,893,161 , GRCh37.p13 chr19: 36,331,303-36,384,063 NPHS1, NFKBID, 4 more genes
    nsv7017094copy number variation1nstd229human GRCh38 chr19: 35,836,784-35,839,790 , GRCh37.p13 chr19: 36,327,686-36,330,692 NPHS1
    nsv7012206copy number variation1nstd229human GRCh38 chr19: 35,833,783-36,008,471 , GRCh37.p13 chr19: 36,324,685-36,499,373 TYROBP, SYNE4, 11 more genes
    nsv7010606copy number variation1nstd229human GRCh38 chr19: 35,809,906-35,825,027 , GRCh37.p13 chr19: 36,300,808-36,315,929 PRODH2, NPHS1
    nsv7007766copy number variation1nstd229human GRCh38 chr19: 35,836,301-35,847,300 , GRCh37.p13 chr19: 36,327,203-36,338,202 NPHS1
    nsv7007723copy number variation1nstd229human GRCh38 chr19: 35,822,251-35,823,447 , GRCh37.p13 chr19: 36,313,153-36,314,349 NPHS1
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7004160copy number variation1nstd229human GRCh38 chr19: 35,835,599-35,849,943 , GRCh37.p13 chr19: 36,326,501-36,340,845 KIRREL2, NPHS1
    nsv7001921copy number variation1nstd229human GRCh38 chr19: 35,824,008-35,838,558 , GRCh37.p13 chr19: 36,314,910-36,329,460 NPHS1
    nsv7001220copy number variation1nstd229human GRCh38 chr19: 35,826,366-35,831,639 , GRCh37.p13 chr19: 36,317,268-36,322,541 NPHS1
    nsv6598388inversion1nstd223human GRCh38 chr19: 35,835,178-35,835,326 , GRCh37.p13 chr19: 36,326,080-36,326,228 NPHS1
    nsv6532655copy number variation1nstd223human GRCh38 chr19: 35,818,262-36,019,433 , GRCh37.p13 chr19: 36,309,164-36,510,335 TYROBP, LOC101927572, 13 more genes
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