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Items: 1 to 20 of 354

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7075108inversion1nstd229human GRCh38 chr16: 22,410,309-22,581,113 , GRCh37.p13 chr16: 22,421,630-22,592,434 NPIPB5, OTOAP1, 4 more genes
    nsv7067843inversion1nstd229human GRCh38 chr16: 21,291,198-22,687,975 , GRCh37.p13 chr16: 21,302,519-22,699,296 SMG1P4, NPIPB5, 41 more genes
    nsv7066172inversion1nstd229human GRCh38 chr16: 21,576,182-22,802,537 , GRCh37.p13 chr16: 21,587,503-22,813,858 UQCRC2, VWA3A, 31 more genes
    nsv7060613inversion1nstd229human GRCh38 chr16: 21,590,269-22,770,847 , GRCh37.p13 chr16: 21,601,590-22,782,168 LOC105371129, OTOAP1, 31 more genes
    nsv7060602inversion1nstd229human GRCh38 chr16: 22,087,809-24,116,610 , GRCh37.p13 chr16: 22,099,130-24,127,931 RRN3P3, MFSD13B, 34 more genes
    nsv7058720inversion1nstd229human GRCh38 chr16: 21,529,628-23,453,946 , GRCh37.p13 chr16: 21,540,949-23,465,267 CDR2-DT, LOC105371131, 40 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
    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
    nsv6623577copy number variation2nstd224human GRCh37 chr16: 22,392,905-22,777,777 , GRCh38.p12 chr16: 22,381,584-22,766,456 SMG1P1, OTOAP1, 5 more genes
    nsv6623195copy number variation1nstd224human GRCh37 chr16: 21,966,869-22,679,456 , GRCh38.p12 chr16: 21,955,548-22,668,135 EEF2K, PDZD9, 19 more genes
    nsv6584124inversion1nstd223human GRCh38 chr16: 21,583,121-22,699,430 , GRCh37.p13 chr16: 21,594,442-22,710,751 ABCA3P1, LOC105371126, 31 more genes
    nsv6578670inversion1nstd223human GRCh38 chr16: 21,590,269-22,770,847 , GRCh37.p13 chr16: 21,601,590-22,782,168 VWA3A, LOC105371131, 31 more genes
    nsv6509012copy number variation1nstd223human GRCh38 chr16: 22,377,547-22,683,420 , GRCh37.p13 chr16: 22,388,868-22,694,741 CDR2-DT, RRN3P3, 6 more genes
    nsv6503803copy number variation1nstd223human GRCh38 chr16: 22,493,301-22,580,800 , GRCh37.p13 chr16: 22,504,622-22,592,121 OTOAP1, LOC112268175, 2 more genes
    nsv6503246copy number variation1nstd223human GRCh38 chr16: 22,438,901-22,595,900 , GRCh37.p13 chr16: 22,450,222-22,607,221 LOC112268175, SMG1P1, 3 more genes
    nsv6496541copy number variation1nstd223human GRCh38 chr16: 22,484,101-22,699,400 , GRCh37.p13 chr16: 22,495,422-22,710,721 OTOAP1, LOC112268175, 3 more genes
    nsv6291667copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr16: 21,761,405-22,710,614 , GRCh38.p12 chr16: 21,750,084-22,699,293 NPIPB5, SMG1P4, 26 more genes
    nsv6290342copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,747,532-22,824,584 , GRCh38.p12 chr16: 21,736,211-22,813,263 SMG1P4, NPIPB5, 28 more genes
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