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Items: 1 to 20 of 74

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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
    nsv4924348copy number variation1nstd200human GRCh38 chr3: 39,404,823-39,420,853 , GRCh37.p13 chr3: 39,446,314-39,462,344 LOC107986075, SNORA6, 2 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
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4085638copy number variation1nstd166human GRCh37.p13 chr3: 39,452,817-39,452,906 , GRCh38.p12 chr3: 39,411,326-39,411,415 RPSA, SNORA62
    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
    nsv3884306copy number variation1nstd102humanUncertain significance GRCh37 chr3: 39,449,057-39,453,982 , GRCh38.p12 chr3: 39,407,566-39,412,491 SNORA62, SNORA6, 1 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
    nsv2165305short tandem repeat5nstd128human GRCh37 chr3: 39,450,576-39,450,595 , GRCh38.p12 chr3: 39,409,085-39,409,104 SNORA62, RPSA
    nsv1143267copy number variation1nstd106human GRCh37 chr3: 74,872-75,298,539 , GRCh38.p12 chr3: 33,198-75,249,388 , TWF2, 1204 more genes
    esv3814945tandem duplication1estd192human GRCh37 chr3: 34,908,715-63,463,093 , GRCh38.p12 chr3: 34,867,223-63,477,417 , PRKCD, 615 more genes
    esv3800699copy number variation1estd192human GRCh37 chr3: 39,384,919-46,465,209 , GRCh38.p12 chr3: 39,343,428-46,423,718 , XCR1, 158 more genes
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