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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv6299964copy number variation1nstd186human GRCh37 chr1: 10,001-52,000 , GRCh38.p12 chr1: 10,001-52,000 OR4G4P, FAM138A, 5 more genes
    nsv6138160copy number variation1nstd206human GRCh38 chr1: 10,000-52,000 , GRCh37.p13 chr1: 10,001-52,000 OR4G4P, FAM138A, 5 more genes
    nsv6113953copy number variation1nstd186human GRCh37 chr1: 11,481-35,484 , GRCh38.p12 chr1: 11,481-35,484 FAM138A, WASH7P, 4 more genes
    nsv5669486inversion1nstd207human GRCh38 chr1: 10,002-347,967 , GRCh37.p13 chr1: 10,002-267,719 , OR4F5, 19 more genes
    nsv5219885copy number variation1nstd204human GRCh38.p13 chr1: 11,601-15,700 , GRCh37.p13 chr1: 11,601-15,700 MIR6859-1, WASH7P, 1 more genes
    nsv5217382copy number variation1nstd204human GRCh38.p13 chr1: 11,601-20,700 , GRCh37.p13 chr1: 11,601-20,700 DDX11L1, MIR6859-1, 1 more genes
    nsv5206588copy number variation1nstd204human GRCh38.p13 chr1: 16,201-20,700 , GRCh37.p13 chr1: 16,201-20,700 WASH7P, MIR6859-1
    nsv5205240copy number variation1nstd204human GRCh38.p13 chr1: 15,801-16,100 , GRCh37.p13 chr1: 15,801-16,100 MIR6859-1, WASH7P
    nsv4728187copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-5,592,835 , GRCh38.p12 chr1: 10,001-5,532,775 UBE2J2, MRPL20, 196 more genes
    nsv4708981copy number variation1nstd195human GRCh37 chr1: 12,801-17,551 , GRCh38.p12 chr1: 12,801-17,551 WASH7P, DDX11L1, 1 more genes
    nsv4593877copy number variation1nstd183human GRCh37 chr1: 13,516-91,073 , GRCh38.p12 chr1: 13,516-91,073 FAM138A, WASH9P, 8 more genes
    nsv4578891copy number variation1nstd183human GRCh37 chr1: 10,529-177,368 , GRCh38.p12 chr1: 10,529-177,368 WASH7P, OR4F5, 13 more genes
    nsv4409157copy number variation1nstd174human GRCh37 chr1: 10,001-82,189 , GRCh38.p12 chr1: 10,001-82,189 OR4F5, OR4G4P, 7 more genes
    nsv4401680copy number variation1nstd174human GRCh37 chr1: 10,499-235,938 , GRCh38.p12 chr1: 10,499-266,187 , LOC729737, 18 more genes
    nsv4398922copy number variation1nstd174human GRCh37 chr1: 10,001-127,330 , GRCh38.p12 chr1: 10,001-127,330 WASH7P, DDX11L1, 9 more genes
    nsv3924689copy number variation1nstd102humanPathogenic NCBI36 chr1: 4,737-7,449,889 , GRCh37.p13 chr1: 14,874-7,527,302 , GRCh38.p12 chr1: 14,874-7,467,242 MIR6726, PLCH2, 230 more genes
    nsv3913374copy number variation1nstd102humanPathogenic NCBI36 chr1: 4,737-8,767,973 , GRCh37.p13 chr1: 14,874-8,845,386 , GRCh38.p12 chr1: 14,874-8,785,327 LOC105378593, TNFRSF9, 252 more genes
    nsv3909879copy number variation1nstd102humanUncertain significance NCBI36 chr1: 4,737-358,524 , GRCh37.p13 chr1: 14,874-368,661 , GRCh38.p12 chr1: 14,874-297,968 RNU6-1100P, DDX11L1, 17 more genes
    nsv3319479copy number variation4nstd162human GRCh38 chr1: 10,401-78,300 , GRCh37.p13 chr1: 10,401-78,300 OR4F5, OR4G4P, 7 more genes
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