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Items: 1 to 20 of 157

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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
    nsv7094831copy number variation1nstd102humanUncertain significance GRCh37 chr16: 27,561,492-27,733,036 , GRCh38.p12 chr16: 27,550,171-27,721,715 KATNIP, GTF3C1, 2 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
    nsv7094776copy number variation1nstd102humanUncertain significance GRCh37 chr16: 27,441,393-28,899,063 , GRCh38.p12 chr16: 27,430,072-28,887,742 SH2B1, RNU6-1241P, 39 more genes
    nsv6996170copy number variation1nstd229human GRCh38 chr16: 27,670,578-27,924,224 , GRCh37.p13 chr16: 27,681,899-27,935,545 LOC100128079, GSG1L, 4 more genes
    nsv6993665copy number variation1nstd229human GRCh38 chr16: 27,710,651-27,712,956 , GRCh37.p13 chr16: 27,721,972-27,724,277 LOC100128079, KATNIP
    nsv6991072copy number variation1nstd229human GRCh38 chr16: 27,709,789-27,713,876 , GRCh37.p13 chr16: 27,721,110-27,725,197 LOC100128079, KATNIP
    nsv6989753copy number variation1nstd229human GRCh38 chr16: 27,513,620-27,735,238 , GRCh37.p13 chr16: 27,524,941-27,746,559 KATNIP, LOC107984874, 2 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
    nsv6623434copy number variation1nstd224human GRCh37 chr16: 27,539,991-27,732,993 , GRCh38.p12 chr16: 27,528,670-27,721,672 LOC107984874, GTF3C1, 2 more genes
    nsv6508222copy number variation1nstd223human GRCh38 chr16: 27,670,578-27,924,229 , GRCh37.p13 chr16: 27,681,899-27,935,550 KATNIP, GSG1L, 4 more genes
    nsv6501228copy number variation1nstd223human GRCh38 chr16: 27,513,620-27,735,237 , GRCh37.p13 chr16: 27,524,941-27,746,558 GTF3C1, LOC107984874, 2 more genes
    nsv6291693copy number variation1nstd102humanUncertain significance GRCh37 chr16: 27,672,420-27,934,033 , GRCh38.p12 chr16: 27,661,099-27,922,712 LOC100128079, RNU6-159P, 4 more genes
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 LOC105371149, SLX1B, 166 more genes
    nsv6289847copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924 GAPDHP35, NSMCE1, 154 more genes
    nsv6236957insertion2nstd214human GRCh38 chr16: 27,713,647-27,713,647 , GRCh37.p13 chr16: 27,724,968-27,724,968 KATNIP, LOC100128079
    nsv6133275copy number variation1nstd213human GRCh37 chr16: 27,410,000-27,770,001 , GRCh38.p12 chr16: 27,398,679-27,758,680 GTF3C1, KATNIP, 5 more genes
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133267copy number variation1nstd213human GRCh37 chr16: 22,710,000-30,200,001 , GRCh38.p12 chr16: 22,698,679-30,188,680 ALDOA, AQP8, 169 more genes
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