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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143297insertion1nstd232human GRCh37.p13 chr16: 29,333,126-29,333,126 , GRCh38.p12 chr16: 29,321,805-29,321,805 SNX29P2
    nsv6980760copy number variation1nstd229human GRCh38 chr16: 29,305,154-29,312,726 , GRCh37.p13 chr16: 29,316,475-29,324,047 SNX29P2
    nsv6638016copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,486,929-29,351,826 , GRCh38.p12 chr16: 28,475,608-29,340,505 ATXN2L, LOC101928188, 33 more genes
    nsv6637786copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,384,464-29,432,245 , GRCh38.p12 chr16: 28,373,143-29,420,924 RABEP2, LOC105371159, 38 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
    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
    nsv6637294copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,490,480-29,379,768 , GRCh38.p12 chr16: 28,479,159-29,368,447 NPIPB9, CDC37P1, 33 more genes
    nsv6637171copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,371,468-29,342,589 , GRCh38.p12 chr16: 28,360,147-29,331,268 LOC105371159, IL27, 38 more genes
    nsv6634416copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,483,659-29,341,550 , GRCh38.p12 chr16: 28,472,338-29,330,229 LOC105371159, RPS15AP33, 33 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
    nsv6513349copy number variation1nstd223human GRCh38 chr16: 29,345,970-29,349,490 , GRCh37.p13 chr16: 29,357,291-29,360,811 SNX29P2
    nsv6512617copy number variation1nstd223human GRCh38 chr16: 29,300,491-29,341,597 , GRCh37.p13 chr16: 29,311,812-29,352,918 SNX29P2
    nsv6509164copy number variation1nstd223human GRCh38 chr16: 29,293,046-29,328,609 , GRCh37.p13 chr16: 29,304,367-29,339,930 LOC105371159, SNX29P2
    nsv6501196copy number variation1nstd223human GRCh38 chr16: 29,310,601-29,312,200 , GRCh37.p13 chr16: 29,321,922-29,323,521 SNX29P2
    nsv6315461copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,349,949-29,342,589 , GRCh38.p12 chr16: 28,338,628-29,331,268 CDC37P2, CDC37P1, 38 more genes
    nsv6291754copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,485,883-29,589,674 , GRCh38.p12 chr16: 28,474,562-29,578,353 SULT1A1, CLN3, 44 more genes
    nsv6291739copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,485,883-29,416,001 , GRCh38.p12 chr16: 28,474,562-29,404,680 ATXN2L, NFATC2IP, 34 more genes
    nsv6291637copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,384,465-29,351,826 , GRCh38.p12 chr16: 28,373,144-29,340,505 SH2B1, CLN3, 37 more genes
    nsv6290312copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 28,353,878-29,478,115 , GRCh38.p12 chr16: 28,342,557-29,466,794 ATP2A1, CD19, 47 more genes
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