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Items: 1 to 20 of 5274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131355insertion1nstd186human GRCh37 chr16: 16,803,588-16,803,633 , GRCh38.p12 chr16|NT_187607.1: 2,370,656-2,370,701 , GRCh38.p12 chr16: 16,709,731-16,709,776 0
    nsv6123247copy number variation1nstd186human GRCh37 chr16: 16,585,407-16,747,857 , GRCh38.p12 chr16: 16,491,550-16,654,000 , GRCh38.p12 chr16|NT_187607.1: 2,152,610-2,314,931 LOC100133127
    nsv6122742copy number variation1nstd186human GRCh37 chr16: 15,359,857-15,371,857 , GRCh38.p12 chr16: 15,266,000-15,278,000 , GRCh38.p12 chr16|NT_187607.1: 384,560-396,561 0
    nsv6122485copy number variation1nstd186human GRCh37 chr16: 16,934,378-16,940,414 , GRCh38.p12 chr16: 16,840,521-16,846,557 , GRCh38.p12 chr16|NT_187607.1: 2,501,427-2,507,461 0
    nsv6122228copy number variation1nstd186human GRCh37 chr16: 16,590,857-16,717,857 , GRCh38.p12 chr16: 16,497,000-16,624,000 , GRCh38.p12 chr16|NT_187607.1: 2,158,060-2,285,054 LOC100133127
    nsv6121750copy number variation1nstd186human GRCh37 chr16: 16,329,757-16,363,857 , GRCh38.p12 chr16|NT_187607.1: 1,893,898-1,928,003 , GRCh38.p12 chr16: 16,235,900-16,270,000 NOMO3
    nsv6121635copy number variation1nstd186human GRCh37 chr16: 16,702,207-16,717,857 , GRCh38.p12 chr16: 16,608,350-16,624,000 , GRCh38.p12 chr16|NT_187607.1: 2,269,410-2,285,054 0
    nsv6121443copy number variation1nstd186human GRCh37 chr16: 16,828,357-16,851,857 , GRCh38.p12 chr16: 16,734,500-16,758,000 , GRCh38.p12 chr16|NT_187607.1: 2,395,436-2,418,936 0
    nsv6121183copy number variation1nstd186human GRCh37 chr16: 16,784,696-16,784,790 , GRCh38.p12 chr16: 16,690,839-16,690,933 , GRCh38.p12 chr16|NT_187607.1: 2,351,763-2,351,857 0
    nsv6120837copy number variation1nstd186human GRCh37 chr16: 16,097,400-16,097,654 , GRCh38.p12 chr16: 16,003,543-16,003,797 , GRCh38.p12 chr16|NT_187607.1: 1,661,421-1,661,675 ABCC1
    nsv6120739copy number variation1nstd186human GRCh37 chr16: 16,329,857-16,339,857 , GRCh38.p12 chr16|NT_187607.1: 1,893,998-1,903,998 , GRCh38.p12 chr16: 16,236,000-16,246,000 NOMO3
    nsv6120578copy number variation1nstd186human GRCh37 chr16: 16,571,857-16,583,857 , GRCh38.p12 chr16: 16,478,000-16,490,000 , GRCh38.p12 chr16|NT_187607.1: 2,139,060-2,151,060 0
    nsv6117476copy number variation1nstd186human GRCh37 chr16: 16,436,857-16,441,857 , GRCh38.p12 chr16|NT_187607.1: 2,002,180-2,007,190 , GRCh38.p12 chr16: 16,343,000-16,348,000 PKD1P1
    nsv6117165mobile element insertion1nstd186human GRCh37 chr16: 16,639,877-16,639,877 , GRCh38.p12 chr16: 16,546,020-16,546,020 , GRCh38.p12 chr16|NT_187607.1: 2,207,080-2,207,080 0
    nsv6116784copy number variation1nstd186human GRCh37 chr16: 16,725,657-16,731,607 , GRCh38.p12 chr16|NT_187607.1: 2,292,737-2,298,685 , GRCh38.p12 chr16: 16,631,800-16,637,750 0
    nsv6115186copy number variation1nstd186human GRCh37 chr16: 14,988,857-14,999,007 , GRCh38.p12 chr16: 14,895,000-14,905,150 , GRCh38.p12 chr16|NT_187607.1: 766,443-773,182 NOMO1, MIR3179-1, 3 more genes
    nsv6113835copy number variation1nstd186human GRCh37 chr16: 16,440,857-16,483,857 , GRCh38.p12 chr16: 16,347,000-16,390,000 , GRCh38.p12 chr16|NT_187607.1: 2,006,190-2,051,042 PKD1P2, PKD1P1, 3 more genes
    nsv6113647copy number variation1nstd186human GRCh37 chr16: 14,781,857-14,855,857 , GRCh38.p12 chr16|NT_187607.1: 291,719-557,969 , GRCh38.p12 chr16: 14,688,000-14,762,000 PDXDC1, LOC105376749, 14 more genes
    nsv6112816copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,887,031-16,308,753 , GRCh38.p12 chr16|NT_187607.1: 326,909-1,872,893 , GRCh38.p12 chr16: 14,793,174-16,214,896 MPV17L, MIR3179-1, 53 more genes
    nsv6112790copy number variation1nstd102humanPathogenic GRCh37 chr16: 16,248,464-16,259,810 , GRCh38.p12 chr16: 16,154,607-16,165,953 , GRCh38.p12 chr16|NT_187607.1: 1,812,535-1,823,883 ABCC6
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