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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5315916copy number variation1nstd204human GRCh38.p13 chr3: 52,412,020-52,414,756 , GRCh37.p13 chr3: 52,446,036-52,448,772 PHF7
    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
    nsv4914344copy number variation1nstd200human GRCh38 chr3: 52,386,019-52,420,329 , GRCh37.p13 chr3: 52,420,035-52,454,345 BAP1, DNAH1, 1 more genes
    nsv4911374copy number variation1nstd200human GRCh38 chr3: 52,416,480-52,419,060 , GRCh37.p13 chr3: 52,450,496-52,453,076 PHF7
    nsv4911373copy number variation1nstd200human GRCh38 chr3: 52,412,029-52,414,749 , GRCh37.p13 chr3: 52,446,045-52,448,765 PHF7
    nsv4911347copy number variation1nstd200human GRCh38 chr3: 51,769,352-52,724,007 , GRCh37.p13 chr3: 51,803,368-52,758,023 , ACY1, 55 more genes
    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
    nsv4793990copy number variation1nstd200human GRCh37 chr3: 52,420,035-52,454,345 , GRCh38.p12 chr3: 52,386,019-52,420,329 PHF7, DNAH1, 1 more genes
    nsv4790720copy number variation1nstd200human GRCh37 chr3: 52,450,496-52,453,076 , GRCh38.p12 chr3: 52,416,480-52,419,060 PHF7
    nsv4790719copy number variation1nstd200human GRCh37 chr3: 52,446,045-52,448,765 , GRCh38.p12 chr3: 52,412,029-52,414,749 PHF7
    nsv4790701copy number variation1nstd200human GRCh37 chr3: 51,803,368-52,758,023 , GRCh38.p12 chr3: 51,769,352-52,724,007 , SNORD19B, 55 more genes
    nsv4733941copy number variation1nstd199human GRCh37 chr3: 52,450,362-52,450,425 , GRCh38.p12 chr3: 52,416,346-52,416,409 PHF7
    nsv4728314copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,975,459-52,561,678 , GRCh38.p12 chr3: 51,941,443-52,527,662 ABHD14A-ACY1, POC1A, 32 more genes
    nsv4682756copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr3: 52,433,063-52,443,894 , GRCh38.p12 chr3: 52,399,047-52,409,878 BAP1, DNAH1, 1 more genes
    nsv4681260copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,436,294-52,443,904 , GRCh38.p12 chr3: 52,402,278-52,409,888 BAP1, PHF7
    nsv4679783copy number variation1nstd189human GRCh37.p13 chr3: 52,082,781-53,128,685 , GRCh38.p12 chr3: 52,048,765-53,094,669 , ALAS1, 50 more genes
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