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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139673copy number variation1nstd232human GRCh37.p13 chr16: 27,503,834-27,503,934 , GRCh38.p12 chr16: 27,492,513-27,492,613 GTF3C1
    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
    nsv7074948inversion1nstd229human GRCh38 chr16: 27,520,744-27,533,100 , GRCh37.p13 chr16: 27,532,065-27,544,421 GTF3C1
    nsv7067709inversion1nstd229human GRCh38 chr16: 27,520,863-27,533,018 , GRCh37.p13 chr16: 27,532,184-27,544,339 GTF3C1
    nsv6993974copy number variation1nstd229human GRCh38 chr16: 27,521,020-27,521,050 , GRCh37.p13 chr16: 27,532,341-27,532,371 GTF3C1
    nsv6990621copy number variation1nstd229human GRCh38 chr16: 27,484,210-27,484,405 , GRCh37.p13 chr16: 27,495,531-27,495,726 GTF3C1
    nsv6990238copy number variation1nstd229human GRCh38 chr16: 27,510,309-27,614,407 , GRCh37.p13 chr16: 27,521,630-27,625,728 GTF3C1, 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
    nsv6989154copy number variation1nstd229human GRCh38 chr16: 27,494,321-27,497,061 , GRCh37.p13 chr16: 27,505,642-27,508,382 GTF3C1
    nsv6983904copy number variation1nstd229human GRCh38 chr16: 27,541,901-27,544,800 , GRCh37.p13 chr16: 27,553,222-27,556,121 GTF3C1
    nsv6983879copy number variation1nstd229human GRCh38 chr16: 27,532,210-27,532,439 , GRCh37.p13 chr16: 27,543,531-27,543,760 GTF3C1
    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
    nsv6513351copy number variation1nstd223human GRCh38 chr16: 27,485,374-27,485,760 , GRCh37.p13 chr16: 27,496,695-27,497,081 GTF3C1
    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
    nsv6499437copy number variation1nstd223human GRCh38 chr16: 27,510,309-27,614,403 , GRCh37.p13 chr16: 27,521,630-27,625,724 KATNIP, GTF3C1
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