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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148094copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,511,270-30,243,006 , GRCh38.p12 chr16: 29,499,949-30,231,685 SMG1P2, KCTD13, 46 more genes
    nsv7137206copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,620,748-30,250,606 , GRCh38.p12 chr16: 29,609,427-30,239,285 SMG1P2, QPRT, 43 more genes
    nsv7137124copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,675,050-30,218,384 , GRCh38.p12 chr16: 29,663,729-30,207,063 LOC112694756, YPEL3-DT, 38 more genes
    nsv7137119copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,495,011-30,206,548 , GRCh38.p12 chr16: 29,483,690-30,195,227 CORO1A-AS1, YPEL3-DT, 42 more genes
    nsv7094835copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,199,895-30,237,215 , GRCh38.p12 chr16: 30,188,574-30,225,894 CORO1A, SLX1A, 6 more genes
    nsv7093394copy number variation1nstd102humannot provided GRCh37 chr16: 29,670,770-30,207,956 , GRCh38.p12 chr16: 29,659,449-30,196,635 LOC105371167, CDIPTOSP, 36 more genes
    nsv7068091inversion1nstd229human GRCh38 chr16: 29,736,414-31,610,190 , GRCh37.p13 chr16: 29,747,735-31,621,511 C16orf92, TMEM219, 118 more genes
    nsv7060598inversion1nstd229human GRCh38 chr16: 30,168,175-31,279,114 , GRCh37.p13 chr16: 30,179,496-31,290,435 ZNF629, ZNF771, 72 more genes
    nsv6637889copy number variation2nstd102humanPathogenic GRCh37 chr16: 29,567,296-30,240,227 , GRCh38.p12 chr16: 29,555,975-30,228,906 MIR3680-2, TLCD3B, 45 more genes
    nsv6637734copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,432,213-30,240,227 , GRCh38.p12 chr16: 29,420,892-30,228,906 SLX1B, LOC606724, 54 more genes
    nsv6637578copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,622,758-30,240,227 , GRCh38.p12 chr16: 29,611,437-30,228,906 PAGR1, SULT1A3, 43 more genes
    nsv6637500copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,731-30,321,320 , GRCh38.p12 chr16: 28,455,410-30,309,999 CA5AP1, NPIPB13, 92 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
    nsv6623639copy number variation1nstd224human GRCh37 chr16: 29,656,093-30,208,522 , GRCh38.p12 chr16: 29,644,772-30,197,201 MAPK3, DOC2A, 36 more genes
    nsv6623443copy number variation1nstd224human GRCh37 chr16: 30,208,520-30,326,963 , GRCh38.p12 chr16: 30,197,199-30,315,642 SULT1A3, SLX1A, 5 more genes
    nsv6623442copy number variation1nstd224human GRCh37 chr16: 30,206,045-30,217,430 , GRCh38.p12 chr16: 30,194,724-30,206,109 SLX1A, LOC613038, 2 more genes
    nsv6623201copy number variation1nstd224human GRCh37 chr16: 29,627,349-30,209,234 , GRCh38.p12 chr16: 29,616,028-30,197,913 ALDOA, KIF22, 38 more genes
    nsv6590041inversion1nstd223human GRCh38 chr16: 29,736,419-31,610,189 , GRCh37.p13 chr16: 29,747,740-31,621,510 MIR762HG, FBXL19, 118 more genes
    nsv6315534copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,628,661-30,306,955 , GRCh38.p12 chr16: 29,617,340-30,295,634 PAGR1, CA5AP1, 42 more genes
    nsv6314862copy number variation1nstd102humanlow penetrance, Likely pathogenic GRCh37.p13 chr16: 29,460,515-30,346,868 , GRCh38 chr16: 29,449,194-30,335,547 ALDOA, CA5AP1, 55 more genes
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