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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137727copy number variation2nstd102humanUncertain significance GRCh38 chr3: 12,589,035-12,766,981 , GRCh37.p13 chr3: 12,630,534-12,808,480 RAF1, CRIP1P1, 1 more genes
    nsv5957942insertion1nstd209human GRCh38 chr3: 12,659,427-12,659,427 , GRCh37.p13 chr3: 12,700,926-12,700,926 RAF1
    nsv5949574insertion1nstd209human GRCh38 chr3: 12,654,687-12,654,687 , GRCh37.p13 chr3: 12,696,186-12,696,186 RAF1
    nsv5901382copy number variation1nstd209human GRCh38 chr3: 11,914,401-12,871,932 , GRCh37.p13 chr3: 11,985,024-12,913,431 SYN2, KRT18P17, 20 more genes
    nsv5900778copy number variation1nstd209human GRCh38 chr3: 12,651,892-12,652,098 , GRCh37.p13 chr3: 12,693,391-12,693,597 RAF1
    nsv5895888copy number variation1nstd209human GRCh38 chr3: 12,589,035-12,766,980 , GRCh37.p13 chr3: 12,630,534-12,808,479 RAF1, TMEM40, 1 more genes
    nsv5894638copy number variation1nstd209human GRCh38 chr3: 12,652,089-12,652,393 , GRCh37.p13 chr3: 12,693,588-12,693,892 RAF1
    nsv5834888copy number variation1nstd209human GRCh38 chr3: 12,636,415-12,683,925 , GRCh37.p13 chr3: 12,677,914-12,725,424 CRIP1P1, RAF1
    nsv5834887copy number variation2nstd209human GRCh38 chr3: 12,636,315-12,638,714 , GRCh37.p13 chr3: 12,677,814-12,680,213 RAF1
    nsv5834635copy number variation1nstd209human GRCh38 chr3: 12,615,615-12,617,784 , GRCh37.p13 chr3: 12,657,114-12,659,283 RAF1
    nsv5834633copy number variation1nstd209human GRCh38 chr3: 12,588,766-12,595,733 , GRCh37.p13 chr3: 12,630,265-12,637,232 RAF1
    nsv5834579copy number variation1nstd209human GRCh38 chr3: 12,623,022-12,631,858 , GRCh37.p13 chr3: 12,664,521-12,673,357 RAF1
    nsv5724377mobile element insertion1nstd211human GRCh38 chr3: 12,641,509-12,641,509 , GRCh37.p13 chr3: 12,683,008-12,683,008 RAF1
    nsv5724075mobile element insertion2nstd211human GRCh38 chr3: 12,623,815-12,623,815 , GRCh37.p13 chr3: 12,665,314-12,665,314 RAF1
    nsv5720424mobile element insertion2nstd211human GRCh38 chr3: 12,654,733-12,654,733 , GRCh37.p13 chr3: 12,696,232-12,696,232 RAF1
    nsv5673473copy number variation1nstd102humanLikely benign GRCh37 chr3: 12,632,277-12,660,220 , GRCh38.p12 chr3: 12,590,778-12,618,721 RAF1
    nsv5618887insertion1nstd207human GRCh38 chr3: 12,623,797-12,623,797 , GRCh37.p13 chr3: 12,665,296-12,665,296 RAF1
    nsv5607760insertion1nstd207human GRCh38 chr3: 12,654,718-12,654,718 , GRCh37.p13 chr3: 12,696,217-12,696,217 RAF1
    nsv5563832sequence alteration1nstd206human GRCh38 chr3: 12,595,568-12,595,579 , GRCh37.p13 chr3: 12,637,067-12,637,078 RAF1
    nsv5451162copy number variation1nstd206human GRCh38 chr3: 12,623,499-12,626,062 , GRCh37.p13 chr3: 12,664,998-12,667,561 RAF1
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