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Items: 1 to 20 of 622

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148123copy number variation2nstd102humanPathogenic GRCh37 chr16: 29,517,464-30,200,058 , GRCh38.p12 chr16: 29,506,143-30,188,737 SMG1P2, QPRT, 39 more genes
    nsv7148104copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,517,464-30,199,839 , GRCh38.p12 chr16: 29,506,143-30,188,518 QPRT, SMG1P2, 39 more genes
    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
    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
    nsv6992715copy number variation1nstd229human GRCh38 chr16: 29,608,471-29,608,496 , GRCh37.p13 chr16: 29,619,792-29,619,817 SMG1P2
    nsv6983480copy number variation1nstd229human GRCh38 chr16: 29,585,102-29,585,147 , GRCh37.p13 chr16: 29,596,423-29,596,468 SMG1P2
    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
    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
    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
    nsv6623638copy number variation1nstd224human GRCh37 chr16: 29,595,483-30,072,530 , GRCh38.p12 chr16: 29,584,162-30,061,209 CA5AP1, HIRIP3, 29 more genes
    nsv6623573copy number variation1nstd224human GRCh37 chr16: 21,525,988-21,777,910 , GRCh38.p12 chr16: 21,514,667-21,766,589 , GRCh38.p12 chr16|NW_017852933.1: 1,338,191-1,590,146 SLC7A5P2, SMG1P2, 8 more genes
    nsv6623438copy number variation1nstd224human GRCh37 chr16: 29,412,503-29,708,612 , GRCh38.p12 chr16: 29,401,182-29,697,291 CA5AP1, QPRT, 15 more genes
    nsv6623200copy number variation3nstd224human GRCh37 chr16: 29,595,483-30,199,713 , GRCh38.p12 chr16: 29,584,162-30,188,392 ALDOA, PPP4C, 38 more genes
    nsv6623199copy number variation1nstd224human GRCh37 chr16: 29,326,560-29,775,947 , GRCh38.p12 chr16: 29,315,239-29,764,626 LOC388242, SNX29P2, 19 more genes
    nsv6507381copy number variation1nstd223human GRCh38 chr16: 29,545,101-29,547,900 , GRCh37.p13 chr16: 29,556,422-29,559,221 SMG1P2
    nsv6507191copy number variation1nstd223human GRCh38 chr16: 29,592,522-29,596,683 , GRCh37.p13 chr16: 29,603,843-29,608,004 LOC105371168, SMG1P2
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