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Items: 1 to 20 of 257

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7061433inversion1nstd229human GRCh38 chr16: 19,893,387-21,501,582 , GRCh37.p13 chr16: 19,904,709-21,512,903 CRYM, SNX29P1, 38 more genes
    nsv6997825copy number variation1nstd229human GRCh38 chr16: 20,768,059-20,856,206 , GRCh37.p13 chr16: 20,779,381-20,867,528 RNU6-944P, DCUN1D3, 4 more genes
    nsv6993173copy number variation1nstd229human GRCh38 chr16: 20,749,897-20,754,356 , GRCh37.p13 chr16: 20,761,219-20,765,678 ACSM3
    nsv6991851copy number variation1nstd229human GRCh38 chr16: 20,770,001-20,774,400 , GRCh37.p13 chr16: 20,781,323-20,785,722 ACSM3
    nsv6991622copy number variation1nstd229human GRCh38 chr16: 20,767,235-20,767,556 , GRCh37.p13 chr16: 20,778,557-20,778,878 ACSM3
    nsv6983909copy number variation1nstd229human GRCh38 chr16: 20,777,530-20,781,800 , GRCh37.p13 chr16: 20,788,852-20,793,122 ERI2, ACSM3
    nsv6980695copy number variation1nstd229human GRCh38 chr16: 20,782,165-20,788,040 , GRCh37.p13 chr16: 20,793,487-20,799,362 ACSM3, RNU6-944P, 1 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
    nsv6637194copy number variation1nstd102humanUncertain significance GRCh37 chr16: 20,631,242-20,784,335 , GRCh38.p12 chr16: 20,619,920-20,773,013 LOC100887080, ACSM1, 2 more genes
    nsv6514717copy number variation1nstd223human GRCh38 chr16: 20,768,058-20,856,205 , GRCh37.p13 chr16: 20,779,380-20,867,527 ACSM3, REXO5, 4 more genes
    nsv6514200copy number variation1nstd223human GRCh38 chr16: 20,781,401-20,782,400 , GRCh37.p13 chr16: 20,792,723-20,793,722 ACSM3, ERI2
    nsv6504803copy number variation1nstd223human GRCh38 chr16: 20,767,219-20,767,539 , GRCh37.p13 chr16: 20,778,541-20,778,861 ACSM3
    nsv6504544copy number variation1nstd223human GRCh38 chr16: 20,790,830-20,792,631 , GRCh37.p13 chr16: 20,802,152-20,803,953 ACSM3, ERI2
    nsv6503063copy number variation1nstd223human GRCh38 chr16: 20,750,988-20,751,477 , GRCh37.p13 chr16: 20,762,310-20,762,799 ACSM3
    nsv6501046copy number variation1nstd223human GRCh38 chr16: 20,767,501-20,770,500 , GRCh37.p13 chr16: 20,778,823-20,781,822 ACSM3
    nsv6250151mobile element insertion1nstd215human GRCh38 chr16: 20,788,535-20,788,535 , GRCh37.p13 chr16: 20,799,857-20,799,857 ACSM3, ERI2
    nsv6250150mobile element insertion1nstd215human GRCh38 chr16: 20,766,322-20,766,322 , GRCh37.p13 chr16: 20,777,644-20,777,644 ACSM3
    nsv6133261copy number variation1nstd213human GRCh37 chr16: 19,140,000-21,360,001 , GRCh38.p12 chr16: 19,128,678-21,348,680 CRYM, GP2, 49 more genes
    nsv6133258copy number variation1nstd213human GRCh37 chr16: 16,530,000-21,500,001 , GRCh38.p12 chr16: 16,436,143-21,488,680 CRYM, GP2, 93 more genes
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