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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898801copy number variation1nstd209human GRCh38 chr3: 46,674,609-46,676,923 , GRCh37.p13 chr3: 46,716,099-46,718,413 ALS2CL
    nsv5895931copy number variation1nstd209human GRCh38 chr3: 46,664,251-46,667,834 , GRCh37.p13 chr3: 46,705,741-46,709,324 ALS2CL
    nsv5836563copy number variation1nstd209human GRCh38 chr3: 46,674,620-46,676,569 , GRCh37.p13 chr3: 46,716,110-46,718,059 ALS2CL
    nsv5835989copy number variation1nstd209human GRCh38 chr3: 46,664,208-46,667,812 , GRCh37.p13 chr3: 46,705,698-46,709,302 ALS2CL
    nsv5583417copy number variation1nstd207human GRCh38 chr3: 46,664,257-46,667,834 , GRCh37.p13 chr3: 46,705,747-46,709,324 ALS2CL
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5447506copy number variation1nstd206human GRCh38 chr3: 46,664,251-46,667,835 , GRCh37.p13 chr3: 46,705,741-46,709,325 ALS2CL
    nsv5387399copy number variation1nstd186human GRCh37 chr3: 46,705,741-46,709,325 , GRCh38.p12 chr3: 46,664,251-46,667,835 ALS2CL
    nsv5307664copy number variation1nstd204human GRCh38.p13 chr3: 46,664,251-46,667,835 , GRCh37.p13 chr3: 46,705,741-46,709,325 ALS2CL
    nsv5213034copy number variation1nstd204human GRCh38.p13 chr3: 46,664,301-46,672,300 , GRCh37.p13 chr3: 46,705,791-46,713,790 ALS2CL
    nsv5209711copy number variation1nstd204human GRCh38.p13 chr3: 46,666,301-46,667,800 , GRCh37.p13 chr3: 46,707,791-46,709,290 ALS2CL
    nsv5209360copy number variation1nstd204human GRCh38.p13 chr3: 46,660,201-46,667,700 , GRCh37.p13 chr3: 46,701,691-46,709,190 ALS2CL
    nsv5206389copy number variation1nstd204human GRCh38.p13 chr3: 46,664,208-46,667,862 , GRCh37.p13 chr3: 46,705,698-46,709,352 ALS2CL
    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
    nsv4911125copy number variation1nstd200human GRCh38 chr3: 46,664,251-46,667,835 , GRCh37.p13 chr3: 46,705,741-46,709,325 ALS2CL
    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
    nsv4790539copy number variation1nstd200human GRCh37 chr3: 46,716,101-46,718,414 , GRCh38.p12 chr3: 46,674,611-46,676,924 ALS2CL
    nsv4790538copy number variation1nstd200human GRCh37 chr3: 46,705,741-46,709,325 , GRCh38.p12 chr3: 46,664,251-46,667,835 ALS2CL
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