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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5900206copy number variation1nstd209human GRCh38 chr3: 123,261,032-123,261,087 , GRCh37.p13 chr3: 122,979,879-122,979,934 SEC22A
    nsv5893626copy number variation1nstd209human GRCh38 chr3: 123,211,827-123,211,947 , GRCh37.p13 chr3: 122,930,674-122,930,794 SEC22A
    nsv5677231mobile element insertion1nstd211human GRCh38 chr3: 123,269,179-123,269,179 , GRCh37.p13 chr3: 122,988,026-122,988,026 SEC22A
    nsv5452844copy number variation1nstd206human GRCh38 chr3: 123,261,033-123,261,088 , GRCh37.p13 chr3: 122,979,880-122,979,935 SEC22A
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919883copy number variation1nstd200human GRCh38 chr3: 123,263,602-123,264,653 , GRCh37.p13 chr3: 122,982,449-122,983,500 SEC22A
    nsv4919882copy number variation1nstd200human GRCh38 chr3: 123,219,043-123,223,291 , GRCh37.p13 chr3: 122,937,890-122,942,138 SEC22A
    nsv4919881copy number variation1nstd200human GRCh38 chr3: 123,218,249-123,223,291 , GRCh37.p13 chr3: 122,937,096-122,942,138 SEC22A
    nsv4919880copy number variation1nstd200human GRCh38 chr3: 123,218,250-123,218,959 , GRCh37.p13 chr3: 122,937,097-122,937,806 SEC22A
    nsv4919879copy number variation1nstd200human GRCh38 chr3: 123,212,367-123,212,564 , GRCh37.p13 chr3: 122,931,214-122,931,411 SEC22A
    nsv4919878copy number variation1nstd200human GRCh38 chr3: 123,211,828-123,211,948 , GRCh37.p13 chr3: 122,930,675-122,930,795 SEC22A
    nsv4807001copy number variation1nstd200human GRCh37 chr3: 122,930,675-122,930,795 , GRCh38.p12 chr3: 123,211,828-123,211,948 SEC22A
    nsv4674011copy number variation1nstd102humanUncertain significance GRCh37 chr3: 122,981,355-123,768,908 , GRCh38.p12 chr3: 123,262,508-124,050,061 ROPN1, LOC105369194, 8 more genes
    nsv4453697copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,384,741-123,672,180 , GRCh38.p12 chr3: 121,665,894-123,953,333 LOC101927010, IQCB1, 35 more genes
    nsv4452620copy number variation1nstd102humanUncertain significance GRCh37 chr3: 122,823,501-123,012,544 , GRCh38.p12 chr3: 123,104,654-123,293,697 PDIA5, ADCY5, 2 more genes
    nsv4451674copy number variation1nstd102humanUncertain significance GRCh37 chr3: 122,991,262-123,242,599 , GRCh38.p12 chr3: 123,272,415-123,523,752 HACD2, ADCY5, 1 more genes
    nsv4450222copy number variation1nstd102humanUncertain significance GRCh37 chr3: 122,827,227-123,114,031 , GRCh38.p12 chr3: 123,108,380-123,395,184 ADCY5, SEC22A, 2 more genes
    nsv4379027copy number variation1nstd173human GRCh37 chr3: 122,906,425-122,950,200 , GRCh38.p12 chr3: 123,187,578-123,231,353 SEC22A
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