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Items: 1 to 20 of 348

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148113copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,834,531-29,001,678 , GRCh38.p12 chr16: 28,823,210-28,990,357 MIR4721, ATP2A1-AS1, 10 more genes
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7094777copy number variation1nstd102humanPathogenic GRCh37 chr16: 27,441,393-29,001,333 , GRCh38.p12 chr16: 27,430,072-28,990,012 NUPR1, RPS15AP33, 45 more genes
    nsv6988461copy number variation1nstd229human GRCh38 chr16: 28,847,661-29,003,536 , GRCh37.p13 chr16: 28,858,982-29,014,857 CD19, RABEP2, 7 more genes
    nsv6986606copy number variation1nstd229human GRCh38 chr16: 28,975,401-28,980,500 , GRCh37.p13 chr16: 28,986,722-28,991,821 SPNS1
    nsv6638016copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,486,929-29,351,826 , GRCh38.p12 chr16: 28,475,608-29,340,505 ATXN2L, LOC101928188, 33 more genes
    nsv6637786copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,384,464-29,432,245 , GRCh38.p12 chr16: 28,373,143-29,420,924 RABEP2, LOC105371159, 38 more genes
    nsv6637784copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,763,835-29,051,191 , GRCh38.p12 chr16: 28,752,514-29,039,870 NPIPB10P, MIR4517, 13 more genes
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637500copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,731-30,321,320 , GRCh38.p12 chr16: 28,455,410-30,309,999 CA5AP1, NPIPB13, 92 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6637294copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,490,480-29,379,768 , GRCh38.p12 chr16: 28,479,159-29,368,447 NPIPB9, CDC37P1, 33 more genes
    nsv6637171copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,371,468-29,342,589 , GRCh38.p12 chr16: 28,360,147-29,331,268 LOC105371159, IL27, 38 more genes
    nsv6634416copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,483,659-29,341,550 , GRCh38.p12 chr16: 28,472,338-29,330,229 LOC105371159, RPS15AP33, 33 more genes
    nsv6623637copy number variation1nstd224human GRCh37 chr16: 28,635,932-29,095,150 , GRCh38.p12 chr16: 28,624,611-29,083,829 EIF3C, SPNS1, 19 more genes
    nsv6623635copy number variation2nstd224human GRCh37 chr16: 28,616,665-29,044,745 , GRCh38.p12 chr16: 28,605,344-29,033,424 ATP2A1, CD19, 19 more genes
    nsv6623592copy number variation1nstd224human GRCh37 chr16: 28,898,537-29,044,745 , GRCh38.p12 chr16: 28,887,216-29,033,424 ATP2A1, CD19, 5 more genes
    nsv6623591copy number variation2nstd224human GRCh37 chr16: 28,826,049-29,044,745 , GRCh38.p12 chr16: 28,814,728-29,033,424 SPNS1, TUFM, 11 more genes
    nsv6623437copy number variation1nstd224human GRCh37 chr16: 28,632,021-29,044,745 , GRCh38.p12 chr16: 28,620,700-29,033,424 ATXN2L, SH2B1, 18 more genes
    nsv6623198copy number variation1nstd224human GRCh37 chr16: 28,603,721-29,044,745 , GRCh38.p12 chr16: 28,592,400-29,033,424 CD19, ATXN2L, 20 more genes
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