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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5453729copy number variation1nstd206human GRCh38 chr3: 38,478,774-38,478,831 , GRCh37.p13 chr3: 38,520,265-38,520,322 ACVR2B
    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
    nsv4910854copy number variation1nstd200human GRCh38 chr3: 38,467,394-38,471,431 , GRCh37.p13 chr3: 38,508,885-38,512,922 ACVR2B
    nsv4910853copy number variation1nstd200human GRCh38 chr3: 38,456,999-38,461,964 , GRCh37.p13 chr3: 38,498,490-38,503,455 ACVR2B
    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
    nsv4806624copy number variation1nstd200human GRCh37 chr3: 38,508,885-38,512,922 , GRCh38.p12 chr3: 38,467,394-38,471,431 ACVR2B
    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
    nsv4674578copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,393,336-38,555,140 , GRCh38.p12 chr3: 38,351,845-38,513,649 ACVR2B, XYLB, 3 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
    nsv4452845copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,518,768-38,674,808 , GRCh38 chr3: 38,477,277-38,633,317 ACVR2B, SCN5A, 3 more genes
    nsv4081244copy number variation1nstd166human GRCh37.p13 chr3: 38,507,778-38,515,675 , GRCh38.p12 chr3: 38,466,287-38,474,184 ACVR2B
    nsv4074768copy number variation1nstd166human GRCh37.p13 chr3: 38,517,016-38,517,119 , GRCh38.p12 chr3: 38,475,525-38,475,628 ACVR2B
    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
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