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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095480copy number variation4nstd102humanUncertain significance GRCh37 chr19: 39,904,727-42,931,301 , GRCh38.p12 chr19: 39,414,087-42,427,149 CYP2B6, EID2B, 140 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7017209copy number variation1nstd229human GRCh38 chr19: 41,206,680-41,209,172 , GRCh37.p13 chr19: 41,712,585-41,715,077 CYP2S1
    nsv7013853copy number variation1nstd229human GRCh38 chr19: 41,186,278-41,191,773 , GRCh37.p13 chr19: 41,692,183-41,697,678 RN7SL718P, CYP2S1
    nsv7012892copy number variation1nstd229human GRCh38 chr19: 41,186,301-41,192,900 , GRCh37.p13 chr19: 41,692,206-41,698,805 RN7SL718P, CYP2S1
    nsv7009629copy number variation1nstd229human GRCh38 chr19: 41,137,056-41,302,288 , GRCh37.p13 chr19: 41,642,961-41,808,193 RN7SL718P, CYP2S1, 6 more genes
    nsv7008207copy number variation1nstd229human GRCh38 chr19: 41,187,401-41,191,800 , GRCh37.p13 chr19: 41,693,306-41,697,705 RN7SL718P, CYP2S1
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7006813copy number variation1nstd229human GRCh38 chr19: 41,187,301-41,191,800 , GRCh37.p13 chr19: 41,693,206-41,697,705 CYP2S1, RN7SL718P
    nsv7003092copy number variation1nstd229human GRCh38 chr19: 41,082,901-41,215,300 , GRCh37.p13 chr19: 41,588,806-41,721,205 CYP2A13, RPL36P16, 4 more genes
    nsv7002740copy number variation1nstd229human GRCh38 chr19: 41,185,301-41,191,800 , GRCh37.p13 chr19: 41,691,206-41,697,705 CYP2S1, RN7SL718P
    nsv7001648copy number variation1nstd229human GRCh38 chr19: 41,199,766-41,211,835 , GRCh37.p13 chr19: 41,705,671-41,717,740 CYP2S1
    nsv6635410copy number variation1nstd227human GRCh38.p12 chr19: 41,154,559-41,198,581 , GRCh37 chr19: 41,660,464-41,704,486 CYP2S1, RPL36P16, 1 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6528687copy number variation1nstd223human GRCh38 chr19: 41,190,048-41,192,268 , GRCh37.p13 chr19: 41,695,953-41,698,173 RN7SL718P, CYP2S1
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5941110copy number variation1nstd209human GRCh38 chr19: 41,186,238-41,191,772 , GRCh37.p13 chr19: 41,692,143-41,697,677 CYP2S1, RN7SL718P
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