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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3892756copy number variation1nstd102humanBenign GRCh37 chr9: 5,162,710-5,213,687 , GRCh38.p12 chr9: 5,162,710-5,213,687 INSL6
    nsv3902975copy number variation1nstd102humanLikely benign GRCh37 chr9: 5,132,122-5,164,251 , GRCh38.p12 chr9: 5,132,122-5,164,251 INSL6
    nsv6311460copy number variation1nstd102humanPathogenic GRCh37 chr2: 152,380,815-152,384,109 , GRCh38.p12 chr2: 151,524,301-151,527,595 RIF1, NEB
    nsv7096201copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 152,348,187-152,425,896 , GRCh38.p12 chr2: 151,491,673-151,569,382 RIF1, NEB
    nsv6291090copy number variation1nstd102humanLikely benign GRCh37 chr9: 5,129,394-5,216,151 , GRCh38.p12 chr9: 5,129,394-5,216,151 INSL6, JAK2
    nsv4729417copy number variation1nstd102humanLikely benign GRCh37 chr9: 5,129,394-5,213,986 , GRCh38.p12 chr9: 5,129,394-5,213,986 JAK2, INSL6
    nsv7095859copy number variation1nstd102humanUncertain significance GRCh37 chr2: 152,369,227-152,376,302 , GRCh38.p12 chr2: 151,512,713-151,519,788 RIF1, NEB
    nsv4453314copy number variation1nstd102humanUncertain significance GRCh37 chr2: 152,352,780-152,354,242 , GRCh38 chr2: 151,496,266-151,497,728 RIF1, NEB
    nsv3872043copy number variation1nstd102humanUncertain significance GRCh37 chr2: 152,353,435-152,354,252 , GRCh38 chr2: 151,496,921-151,497,738 RIF1, NEB
    nsv3875659copy number variation1nstd102humanUncertain significance GRCh37 chr2: 152,353,435-152,353,567 , GRCh38 chr2: 151,496,921-151,497,053 RIF1, NEB
    nsv4683530copy number variation1nstd102humanUncertain significance GRCh37 chr2: 152,353,445-152,353,557 , GRCh38.p12 chr2: 151,496,931-151,497,043 RIF1, NEB
    nsv3924733copy number variation1nstd102humanUncertain significance GRCh37 chr9: 5,116,731-5,216,903 , GRCh38 chr9: 5,116,731-5,216,903 , NCBI36 chr9: 5,106,731-5,206,903 JAK2, INSL6
    nsv6311294copy number variation1nstd102humanUncertain significance GRCh37 chr2: 152,342,274-152,432,888 , GRCh38.p12 chr2: 151,485,760-151,576,374 RIF1, NEB
    nsv3894379copy number variation1nstd102humanconflicting data from submitters GRCh37 chr9: 5,126,597-5,185,255 , GRCh38.p12 chr9: 5,126,597-5,185,255 INSL6, JAK2
    nsv4681057copy number variation1nstd102humanPathogenic GRCh37 chr2: 152,342,264-152,814,130 , GRCh38.p12 chr2: 151,485,750-151,957,616 RIF1, NEB, 2 more genes
    nsv3899311copy number variation1nstd102humanBenign GRCh37 chr9: 5,112,844-5,230,447 , GRCh38.p12 chr9: 5,112,844-5,230,447 INSL6, INSL4, 3 more genes
    nsv7098936copy number variation1nstd102humanUncertain significance GRCh38 chr2: 151,451,642-151,807,929 , GRCh37.p13 chr2: 152,308,156-152,664,443 RIF1, ARL5A, 1 more genes
    nsv3896531copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,883,256-5,037,444 , GRCh38.p12 chr9: 4,883,256-5,037,444 HNRNPA1P41, JAK2, 1 more genes
    nsv6634468copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,959,024-5,072,846 , GRCh38.p12 chr9: 4,959,024-5,072,846 CSNK1G2P1, INSL6, 1 more genes
    nsv4728976copy number variation1nstd102humanUncertain significance GRCh37 chr9: 5,110,389-5,213,986 , GRCh38.p12 chr9: 5,110,389-5,213,986 MTND5P14, INSL6, 3 more genes
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