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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098909copy number variation1nstd102humanUncertain significance GRCh38 chr15: 45,092,835-45,433,283 , GRCh37.p13 chr15: 45,385,033-45,725,481 C15orf48, AFG2B, 17 more genes
    nsv7094711copy number variation1nstd102humanUncertain significance GRCh37 chr15: 45,152,372-45,670,651 , GRCh38.p12 chr15: 44,860,174-45,378,453 TRH-GTG1-8, H3P39, 25 more genes
    nsv7094377copy number variation1nstd102humanUncertain significance GRCh37 chr15: 45,656,975-45,884,494 , GRCh38.p12 chr15: 45,364,777-45,592,296 C15orf48, AFG2B, 10 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6975075copy number variation1nstd229human GRCh38 chr15: 45,390,729-45,390,746 , GRCh37.p13 chr15: 45,682,927-45,682,944 GATM
    nsv6974702copy number variation1nstd229human GRCh38 chr15: 45,305,871-45,405,731 , GRCh37.p13 chr15: 45,598,069-45,697,929 AFG2B, LOC107984732, 3 more genes
    nsv6972994copy number variation1nstd229human GRCh38 chr15: 45,112,133-45,444,447 , GRCh37.p13 chr15: 45,404,331-45,736,645 H3P39, TRH-GTG1-8, 18 more genes
    nsv6972342copy number variation1nstd229human GRCh38 chr15: 45,377,801-45,409,000 , GRCh37.p13 chr15: 45,669,999-45,701,198 AFG2B, GATM
    nsv6965794copy number variation1nstd229human GRCh38 chr15: 45,391,501-45,398,300 , GRCh37.p13 chr15: 45,683,699-45,690,498 GATM
    nsv6962556copy number variation1nstd229human GRCh38 chr15: 45,315,696-45,937,560 , GRCh37.p13 chr15: 45,607,894-46,229,758 LOC107987223, MIR147B, 16 more genes
    nsv6961575copy number variation1nstd229human GRCh38 chr15: 44,757,685-45,480,791 , GRCh37.p13 chr15: 45,049,883-45,772,989 SORD, C15orf48, 34 more genes
    nsv6500185copy number variation1nstd223human GRCh38 chr15: 45,391,474-45,398,301 , GRCh37.p13 chr15: 45,683,672-45,690,499 GATM
    nsv6242011mobile element insertion1nstd215human GRCh38 chr15: 45,384,149-45,384,149 , GRCh37.p13 chr15: 45,676,347-45,676,347 GATM
    nsv5380762copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-45,898,712 , GRCh38.p12 chr15: 44,563,121-45,606,514 LOC100533853, RNU6-1108P, 44 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005337copy number variation1nstd200human GRCh38 chr15: 44,757,662-45,480,882 , GRCh37.p13 chr15: 45,049,860-45,773,080 DUOXA1, TRH-GTG1-7, 34 more genes
    nsv5005336copy number variation1nstd200human GRCh38 chr15: 44,757,739-45,467,369 , GRCh37.p13 chr15: 45,049,937-45,759,567 TRH-GTG1-9, LOC100533853, 33 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4729351copy number variation1nstd102humanUncertain significance GRCh37 chr15: 45,056,077-45,772,378 , GRCh38.p12 chr15: 44,763,879-45,480,180 LOC100187725, DUOXA2, 34 more genes
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