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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959282insertion1nstd209human GRCh38 chr3: 39,072,125-39,072,125 , GRCh37.p13 chr3: 39,113,616-39,113,616 WDR48
    nsv5204022copy number variation1nstd204human GRCh38.p13 chr3: 39,032,080-39,054,308 , GRCh37.p13 chr3: 39,073,571-39,095,799 SCN11A, WDR48
    nsv5066194mobile element insertion1nstd203human GRCh38 chr3: 39,078,585-39,078,585 , GRCh37.p13 chr3: 39,120,076-39,120,076 WDR48
    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
    nsv4924345copy number variation1nstd200human GRCh38 chr3: 39,078,915-39,112,331 , GRCh37.p13 chr3: 39,120,406-39,153,822 TTC21A, GORASP1, 1 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
    nsv4596452copy number variation1nstd183human GRCh37 chr3: 39,071,428-39,121,023 , GRCh38.p12 chr3: 39,029,937-39,079,532 SCN11A, WDR48
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4470918mobile element insertion1nstd166human GRCh37.p13 chr3: 39,104,806-39,104,806 , GRCh38.p12 chr3: 39,063,315-39,063,315 WDR48
    nsv4369064copy number variation1nstd173human GRCh37 chr3: 38,610,945-39,118,719 , GRCh38.p12 chr3: 38,569,454-39,077,228 LOC107986042, SCN10A, 5 more genes
    nsv4086503copy number variation1nstd166human GRCh37.p13 chr3: 39,101,894-39,101,945 , GRCh38.p12 chr3: 39,060,403-39,060,454 WDR48
    nsv3963225copy number variation1nstd168human GRCh38 chr3: 39,066,114-39,088,577 , GRCh37.p13 chr3: 39,107,605-39,130,068 WDR48
    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
    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
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