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Items: 1 to 20 of 888

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629445copy number variation1nstd224human GRCh37 chr4: 48,546,009-49,091,782 , GRCh38.p12 chr4: 48,543,992-49,089,765 OCIAD1, CWH43, 6 more genes
    nsv6282263insertion1nstd214human GRCh38 chr4: 48,656,309-48,656,309 , GRCh37.p13 chr4: 48,658,326-48,658,326 FRYL
    nsv6276174insertion1nstd214human GRCh38 chr4: 48,656,317-48,656,317 , GRCh37.p13 chr4: 48,658,334-48,658,334 FRYL
    nsv6264453copy number variation1nstd214human GRCh38 chr4: 48,539,035-48,539,115 , GRCh37.p13 chr4: 48,541,052-48,541,132 FRYL
    nsv6244060mobile element insertion1nstd215human GRCh38 chr4: 48,662,646-48,662,646 , GRCh37.p13 chr4: 48,664,663-48,664,663 FRYL
    nsv6216358insertion1nstd214human GRCh38 chr4: 48,656,308-48,656,308 , GRCh37.p13 chr4: 48,658,325-48,658,325 FRYL
    nsv6079485insertion1nstd212human GRCh38 chr4: 48,645,135-48,645,135 , GRCh37.p13 chr4: 48,647,152-48,647,152 FRYL
    nsv6077995insertion1nstd212human GRCh38 chr4: 48,632,127-48,632,127 , GRCh37.p13 chr4: 48,634,144-48,634,144 FRYL
    nsv6071581insertion1nstd212human GRCh38 chr4: 48,580,250-48,580,250 , GRCh37.p13 chr4: 48,582,267-48,582,267 FRYL
    nsv6069074insertion1nstd212human GRCh38 chr4: 48,764,720-48,764,720 , GRCh37.p13 chr4: 48,766,737-48,766,737 FRYL
    nsv6062416insertion1nstd212human GRCh38 chr4: 48,656,317-48,656,317 , GRCh37.p13 chr4: 48,658,334-48,658,334 FRYL
    nsv5997729copy number variation1nstd212human GRCh38 chr4: 48,716,258-48,720,221 , GRCh37.p13 chr4: 48,718,275-48,722,238 FRYL
    nsv5997344copy number variation1nstd212human GRCh38 chr4: 48,659,523-48,659,919 , GRCh37.p13 chr4: 48,661,540-48,661,936 FRYL
    nsv5997343copy number variation1nstd212human GRCh38 chr4: 48,659,405-48,659,507 , GRCh37.p13 chr4: 48,661,422-48,661,524 FRYL
    nsv5952743insertion1nstd209human GRCh38 chr4: 48,659,919-48,659,919 , GRCh37.p13 chr4: 48,661,936-48,661,936 FRYL
    nsv5904754copy number variation1nstd209human GRCh38 chr4: 48,656,085-48,656,165 , GRCh37.p13 chr4: 48,658,102-48,658,182 FRYL
    nsv5898480copy number variation1nstd209human GRCh38 chr4: 48,659,454-48,659,921 , GRCh37.p13 chr4: 48,661,471-48,661,938 FRYL
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