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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894762copy number variation1nstd209human GRCh38 chr3: 48,237,809-48,249,293 , GRCh37.p13 chr3: 48,279,299-48,290,783 ZNF589
    nsv5836313copy number variation1nstd209human GRCh38 chr3: 48,238,390-48,246,250 , GRCh37.p13 chr3: 48,279,880-48,287,740 ZNF589
    nsv5694308mobile element insertion2nstd211human GRCh38 chr3: 48,262,690-48,262,690 , GRCh37.p13 chr3: 48,304,180-48,304,180 ZNF589
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5449344copy number variation1nstd206human GRCh38 chr3: 48,239,914-48,240,165 , GRCh37.p13 chr3: 48,281,404-48,281,655 ZNF589
    nsv5443296copy number variation1nstd206human GRCh38 chr3: 48,238,325-48,239,248 , GRCh37.p13 chr3: 48,279,815-48,280,738 ZNF589
    nsv5442959copy number variation1nstd206human GRCh38 chr3: 48,268,838-48,269,315 , GRCh37.p13 chr3: 48,310,328-48,310,805 ZNF589
    nsv5437350copy number variation1nstd206human GRCh38 chr3: 48,248,258-48,253,360 , GRCh37.p13 chr3: 48,289,748-48,294,850 ZNF589
    nsv5412976mobile element insertion1nstd206human GRCh38 chr3: 48,262,690-48,262,741 , GRCh37.p13 chr3: 48,304,180-48,304,231 ZNF589
    nsv5384931mobile element deletion1nstd186human GRCh37 chr3: 48,280,622-48,280,930 , GRCh38.p12 chr3: 48,239,132-48,239,440 ZNF589
    nsv5382879mobile element deletion1nstd186human GRCh37 chr3: 48,280,624-48,280,929 , GRCh38.p12 chr3: 48,239,134-48,239,439 ZNF589
    nsv5307093copy number variation1nstd204human GRCh38.p13 chr3: 48,249,366-48,250,670 , GRCh37.p13 chr3: 48,290,856-48,292,160 ZNF589
    nsv5065132mobile element insertion1nstd203human GRCh38 chr3: 48,262,674-48,262,690 , GRCh37.p13 chr3: 48,304,164-48,304,180 ZNF589
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924420copy number variation1nstd200human GRCh38 chr3: 48,238,220-48,239,292 , GRCh37.p13 chr3: 48,279,710-48,280,782 ZNF589
    nsv4911191copy number variation1nstd200human GRCh38 chr3: 48,249,312-48,250,704 , GRCh37.p13 chr3: 48,290,802-48,292,194 ZNF589
    nsv4888853mobile element deletion1nstd200human GRCh38 chr3: 48,239,132-48,239,440 , GRCh37.p13 chr3: 48,280,622-48,280,930 ZNF589
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
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