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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112739copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 41,265,560-41,280,833 , GRCh38.p12 chr3: 41,224,069-41,239,342 CTNNB1
    nsv5622403insertion1nstd207human GRCh38 chr3: 41,198,758-41,198,758 , GRCh37.p13 chr3: 41,240,249-41,240,249 CTNNB1
    nsv5448221copy number variation1nstd206human GRCh38 chr3: 41,198,000-41,198,121 , GRCh37.p13 chr3: 41,239,491-41,239,612 CTNNB1
    nsv5079648mobile element insertion1nstd203human GRCh38 chr3: 41,208,795-41,208,812 , GRCh37.p13 chr3: 41,250,286-41,250,303 CTNNB1
    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
    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
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4470616mobile element insertion1nstd166human GRCh37.p13 chr3: 41,250,286-41,250,286 , GRCh38.p12 chr3: 41,208,795-41,208,795 CTNNB1
    nsv4090064copy number variation1nstd166human GRCh37.p13 chr3: 41,281,427-41,281,488 , GRCh38.p12 chr3: 41,239,936-41,239,997 CTNNB1
    nsv4081174copy number variation1nstd166human GRCh37.p13 chr3: 41,270,381-41,271,284 , GRCh38.p12 chr3: 41,228,890-41,229,793 CTNNB1
    nsv4078257copy number variation1nstd166human GRCh37.p13 chr3: 41,269,706-41,270,079 , GRCh38.p12 chr3: 41,228,215-41,228,588 CTNNB1
    nsv3905127copy number variation1nstd102humanPathogenic GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521 LINC02022, RPL23AP43, 540 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 RNU6-243P, ZNF385D, 382 more genes
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 ACAA1, ACVR2B, 344 more genes
    nsv3881275copy number variation1nstd102humanPathogenic GRCh37 chr3: 41,104,508-44,636,698 , GRCh38.p12 chr3: 41,063,017-44,595,206 LOC107986077, LOC105377052, 69 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
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