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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5351681translocation1nstd200human GRCh38 chr3: 40,466,544-40,466,544 , GRCh38 chr3: 40,466,434-40,466,434 , GRCh37.p13 chr3: 40,507,925-40,507,925 , GRCh37.p13 chr3: 40,508,035-40,508,035 RPL14
    nsv5351680translocation1nstd200human GRCh38 chr3: 40,459,975-40,459,975 , GRCh38 chr3: 40,459,924-40,459,924 , GRCh37.p13 chr3: 40,501,415-40,501,415 , GRCh37.p13 chr3: 40,501,466-40,501,466 RPL14
    nsv5063729mobile element insertion1nstd203human GRCh38 chr3: 40,456,761-40,456,777 , GRCh37.p13 chr3: 40,498,252-40,498,268 RPL14
    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
    nsv4910909copy number variation1nstd200human GRCh38 chr3: 40,468,129-40,484,180 , GRCh37.p13 chr3: 40,509,620-40,525,671 RPL14, ZNF619
    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
    nsv4806668copy number variation1nstd200human GRCh37 chr3: 40,509,620-40,525,671 , GRCh38.p12 chr3: 40,468,129-40,484,180 RPL14, ZNF619
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4368559copy number variation1nstd173human GRCh37 chr3: 40,491,441-40,568,967 , GRCh38.p12 chr3: 40,449,950-40,527,476 RPL14, ZNF620, 4 more genes
    nsv4075382copy number variation1nstd166human GRCh37.p13 chr3: 40,494,000-40,500,500 , GRCh38.p12 chr3: 40,452,509-40,459,009 ENTPD3-AS1, RPL14
    nsv3917642copy number variation1nstd102humanPathogenic NCBI36 chr3: 33,744,902-40,678,946 , GRCh37 chr3: 33,769,898-40,703,942 , GRCh38 chr3: 33,728,406-40,662,451 STAC, SCN11A, 111 more genes
    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
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3168877copy number variation1nstd158human GRCh37 chr3: 38,483,456-71,473,806 , GRCh38.p12 chr3: 38,441,965-71,424,655 , ACVR2B, 646 more genes
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