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Items: 1 to 20 of 73

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964714insertion1nstd209human GRCh38 chr3: 42,468,068-42,468,068 , GRCh37.p13 chr3: 42,509,560-42,509,560 RPL35AP8
    nsv5963403insertion1nstd209human GRCh38 chr3: 42,469,073-42,469,073 , GRCh37.p13 chr3: 42,510,565-42,510,565 RPL35AP8
    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
    nsv4728413copy number variation1nstd102humanUncertain significance GRCh37 chr3: 42,008,472-42,610,176 , GRCh38.p12 chr3: 41,966,980-42,568,684 LYZL4, SEC22C, 12 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
    nsv3914992copy number variation1nstd102humanUncertain significance GRCh37 chr3: 41,921,995-42,591,771 , GRCh38 chr3: 41,880,503-42,550,279 , NCBI36 chr3: 41,896,999-42,566,775 CCK, EIF4BP4, 14 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
    nsv3168877copy number variation1nstd158human GRCh37 chr3: 38,483,456-71,473,806 , GRCh38.p12 chr3: 38,441,965-71,424,655 , ACVR2B, 646 more genes
    nsv3132947copy number variation1nstd151human GRCh37 chr3: 41,877,353-43,390,054 , GRCh38.p12 chr3: 41,835,861-43,348,562 HHATL, EIF4BP4, 42 more genes
    nsv3118775copy number variation1nstd151human GRCh37 chr3: 41,925,363-42,605,183 , GRCh38.p12 chr3: 41,883,871-42,563,691 ULK4, SALL4P6, 14 more genes
    nsv2768229copy-neutral loss of heterozygosity1nstd125human GRCh37 chr3: 39,873,604-53,004,620 , GRCh38.p12 chr3: 39,832,113-52,970,604 , ACY1, 400 more genes
    nsv2163275short tandem repeat2nstd128human GRCh37 chr3: 42,511,597-42,511,607 , GRCh38.p12 chr3: 42,470,105-42,470,115 RPL35AP8
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