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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
    nsv7074858inversion1nstd229human GRCh38 chr16: 16,637,702-18,721,515 , GRCh37.p13 chr16: 16,731,559-18,732,837 LOC105376751, PKD1P5, 27 more genes
    nsv7071896inversion1nstd229human GRCh38 chr16: 16,594,753-18,758,882 , GRCh37.p13 chr16: 16,688,610-18,770,204 LOC107987234, LOC105379460, 27 more genes
    nsv7069945inversion1nstd229human GRCh38 chr16: 16,637,744-18,721,512 , GRCh37.p13 chr16: 16,731,601-18,732,834 MIR3179-4, PKD1P4-NPIPA8, 27 more genes
    nsv7068202inversion1nstd229human GRCh38 chr16: 17,934,050-18,706,616 , GRCh37.p13 chr16: 18,027,907-18,717,938 MIR3670-3, MIR3670-4, 20 more genes
    nsv7067918inversion1nstd229human GRCh38 chr16: 14,867,200-18,528,889 , GRCh37.p13 chr16: 14,961,057-18,540,211 NPIPA1, NDE1, 80 more genes
    nsv7065228inversion1nstd229human GRCh38 chr16: 16,206,939-18,587,719 , GRCh37.p13 chr16: 16,300,796-18,599,041 NPIPA7, LOC105371106, 42 more genes
    nsv7065205inversion1nstd229human GRCh38 chr16: 17,075,131-18,695,381 , GRCh37.p13 chr16: 17,168,988-18,706,703 MIR3179-3, NOMO2, 26 more genes
    nsv7062654inversion1nstd229human GRCh38 chr16: 16,571,414-18,782,671 , GRCh37.p13 chr16: 16,665,271-18,793,993 PKD1P4-NPIPA8, LOC102723692, 28 more genes
    nsv7058379inversion1nstd229human GRCh38 chr16: 16,196,635-18,896,827 , GRCh37.p13 chr16: 16,290,492-18,908,149 LOC105376751, NOMO3, 46 more genes
    nsv6966433copy number variation1nstd229human GRCh38 chr16: 17,335,724-19,726,946 , GRCh37.p13 chr16: 17,429,581-19,738,268 MIR3179-4, GDE1, 45 more genes
    nsv6637991copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,316,939-18,770,833 , GRCh38.p12 chr16: 15,223,082-18,759,511 ABCC6, ABCC1, 58 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
    nsv6634451copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,458,733-18,520,588 , GRCh38.p12 chr16: 15,364,876-18,426,731 , GRCh38.p12 chr16|NT_187607.1: 1,022,822-2,659,700 ABCC6, ABCC1, 52 more genes
    nsv6623564copy number variation1nstd224human GRCh37 chr16: 18,255,924-18,768,776 , GRCh38.p12 chr16: 18,162,067-18,757,454 MIR3670-3, MIR3179-4, 18 more genes
    nsv6315527copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,416,917-18,770,833 , GRCh38.p12 chr16: 15,323,060-18,759,511 LOC107984869, PKD1P5, 57 more genes
    nsv6315503copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,316,618-18,770,833 , GRCh38.p12 chr16: 15,222,761-18,759,511 ABCC6, ABCC1, 58 more genes
    nsv6307583copy number variation1nstd186human GRCh37 chr16: 18,419,007-18,491,857 , GRCh38.p12 chr16: 18,325,150-18,398,000 , PKD1P5, 7 more genes
    nsv6307547copy number variation1nstd186human GRCh37 chr16: 18,411,857-18,435,857 , GRCh38.p12 chr16: 18,318,000-18,342,000 , PKD1P4, 2 more genes
    nsv6307398copy number variation1nstd186human GRCh37 chr16: 18,411,857-18,419,857 , GRCh38.p12 chr16: 18,318,000-18,326,000 , NPIPA8, 1 more genes
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