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Items: 1 to 20 of 64

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4681830copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,493,856-38,991,863 , GRCh38.p12 chr3: 37,452,365-38,950,372 ITGA9-AS1, SLC22A14, 30 more genes
    nsv4674307copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,987,092-38,194,369 , GRCh38.p12 chr3: 37,945,601-38,152,878 PLCD1, MIR26A1, 7 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
    nsv4453595copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,493,856-38,991,863 , GRCh38 chr3: 37,452,365-38,950,372 DLEC1P1, LOC105377034, 30 more genes
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 RN7SL4P, TOP2B, 348 more genes
    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
    nsv3884510copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,891,706-38,877,793 , GRCh38.p12 chr3: 37,850,215-38,836,302 EXOG, SCN10A, 25 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
    nsv3874556copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,021,661-38,510,752 , GRCh38.p12 chr3: 37,980,170-38,469,261 XYLB, MYD88, 16 more genes
    nsv3872215copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,493,846-38,991,873 , GRCh38.p12 chr3: 37,452,355-38,950,382 ITGA9-AS1, RPL18AP7, 30 more genes
    nsv3127860copy number variation1nstd151human GRCh37 chr3: 38,125,646-38,359,745 , GRCh38.p12 chr3: 38,084,155-38,318,254 ACAA1, DLEC1, 8 more genes
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