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Items: 1 to 20 of 78

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5436010copy number variation1nstd206human GRCh38 chr3: 42,665,757-42,666,108 , GRCh37.p13 chr3: 42,707,249-42,707,600 ZBTB47
    nsv5315054copy number variation1nstd204human GRCh37.p13 chr3: 42,687,395-42,694,227 , GRCh38.p13 chr3: 42,645,903-42,652,735 NKTR, ZBTB47, 1 more genes
    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
    nsv4790445copy number variation1nstd200human GRCh37 chr3: 42,687,399-42,694,218 , GRCh38.p12 chr3: 42,645,907-42,652,726 ZBTB47, NKTR, 1 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
    nsv3969126copy number variation1nstd168human GRCh38 chr3: 42,663,750-42,677,000 , GRCh37.p13 chr3: 42,705,242-42,718,492 RN7SL567P, ZBTB47
    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
    nsv3875334copy number variation1nstd102humanBenign GRCh37 chr3: 42,578,509-42,723,605 , GRCh38.p12 chr3: 42,537,017-42,682,113 NKTR, VIPR1, 5 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
    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
    nsv2164679short tandem repeat1nstd128human GRCh37 chr3: 42,695,785-42,695,812 , GRCh38.p12 chr3: 42,654,293-42,654,320 ZBTB47-AS1, ZBTB47
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