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Items: 1 to 20 of 193

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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
    nsv7075256inversion1nstd229human GRCh38 chr16: 20,048,198-20,057,468 , GRCh37.p13 chr16: 20,059,520-20,068,790 GPR139
    nsv7067520inversion1nstd229human GRCh38 chr16: 20,074,319-20,076,424 , GRCh37.p13 chr16: 20,085,641-20,087,746 GPR139
    nsv7061433inversion1nstd229human GRCh38 chr16: 19,893,387-21,501,582 , GRCh37.p13 chr16: 19,904,709-21,512,903 CRYM, SNX29P1, 38 more genes
    nsv6988458copy number variation1nstd229human GRCh38 chr16: 20,042,955-20,056,156 , GRCh37.p13 chr16: 20,054,277-20,067,478 GPR139
    nsv6988001copy number variation1nstd229human GRCh38 chr16: 20,055,701-20,062,100 , GRCh37.p13 chr16: 20,067,023-20,073,422 GPR139
    nsv6979226copy number variation1nstd229human GRCh38 chr16: 20,037,601-20,046,400 , GRCh37.p13 chr16: 20,048,923-20,057,722 GPR139
    nsv6978585copy number variation1nstd229human GRCh38 chr16: 20,061,225-20,061,262 , GRCh37.p13 chr16: 20,072,547-20,072,584 GPR139
    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
    nsv6581347inversion1nstd223human GRCh38 chr16: 20,037,233-20,037,923 , GRCh37.p13 chr16: 20,048,555-20,049,245 GPR139
    nsv6513688copy number variation1nstd223human GRCh38 chr16: 20,030,707-20,031,292 , GRCh37.p13 chr16: 20,042,029-20,042,614 GPR139
    nsv6497973copy number variation1nstd223human GRCh38 chr16: 20,040,901-20,043,700 , GRCh37.p13 chr16: 20,052,223-20,055,022 GPR139
    nsv6275231copy number variation1nstd214human GRCh38 chr16: 20,041,122-20,041,196 , GRCh37.p13 chr16: 20,052,444-20,052,518 GPR139
    nsv6271195copy number variation1nstd214human GRCh38 chr16: 20,041,127-20,041,196 , GRCh37.p13 chr16: 20,052,449-20,052,518 GPR139
    nsv6250142mobile element insertion1nstd215human GRCh38 chr16: 20,041,233-20,041,233 , GRCh37.p13 chr16: 20,052,555-20,052,555 GPR139
    nsv6203211copy number variation1nstd214human GRCh38 chr16: 20,041,211-20,041,260 , GRCh37.p13 chr16: 20,052,533-20,052,582 GPR139
    nsv6202254copy number variation1nstd214human GRCh38 chr16: 20,041,147-20,041,196 , GRCh37.p13 chr16: 20,052,469-20,052,518 GPR139
    nsv6200463copy number variation1nstd214human GRCh38 chr16: 20,061,178-20,061,237 , GRCh37.p13 chr16: 20,072,500-20,072,559 GPR139
    nsv6192159copy number variation1nstd214human GRCh38 chr16: 20,041,142-20,041,196 , GRCh37.p13 chr16: 20,052,464-20,052,518 GPR139
    nsv6191140copy number variation1nstd214human GRCh38 chr16: 20,041,113-20,041,197 , GRCh37.p13 chr16: 20,052,435-20,052,519 GPR139
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