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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919109copy number variation1nstd209human GRCh38 chr8: 61,899,888-61,911,208 , GRCh37.p13 chr8: 62,812,447-62,823,767 LINC02842, C1GALT1P3
    nsv5910396copy number variation1nstd209human GRCh38 chr8: 61,899,964-61,911,095 , GRCh37.p13 chr8: 62,812,523-62,823,654 C1GALT1P3, LINC02842
    nsv5854767copy number variation1nstd209human GRCh38 chr8: 61,900,067-61,910,962 , GRCh37.p13 chr8: 62,812,626-62,823,521 LINC02842, C1GALT1P3
    nsv5490119copy number variation1nstd206human GRCh38 chr8: 61,867,080-61,925,599 , GRCh37.p13 chr8: 62,779,639-62,838,158 LINC02842, C1GALT1P3, 1 more genes
    nsv4960558copy number variation1nstd200human GRCh38 chr8: 61,669,882-61,969,531 , GRCh37.p13 chr8: 62,582,441-62,882,090 ASPH, MIR4470, 4 more genes
    nsv4813320copy number variation1nstd200human GRCh37 chr8: 62,582,441-62,882,090 , GRCh38.p12 chr8: 61,669,882-61,969,531 ASPH, MIR4470, 4 more genes
    nsv4716589copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 60,026,663-63,779,735 , GRCh38.p12 chr8: 59,114,104-62,867,176 ASPH, CA8, 36 more genes
    nsv4603938copy number variation2nstd183human GRCh37 chr8: 62,737,007-62,862,591 , GRCh38.p12 chr8: 61,824,448-61,950,032 LINC02842, C1GALT1P3, 2 more genes
    nsv4603212copy number variation1nstd183human GRCh37 chr8: 62,734,112-62,856,100 , GRCh38.p12 chr8: 61,821,553-61,943,541 LOC105375871, LINC02842, 2 more genes
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4455899copy number variation1nstd102humanUncertain significance GRCh37 chr8: 62,544,294-63,317,174 , GRCh38.p12 chr8: 61,631,735-62,404,615 RN7SKP97, NARS1P2, 9 more genes
    nsv4399894copy number variation1nstd174human GRCh37 chr8: 62,517,980-62,873,803 , GRCh38.p12 chr8: 61,605,421-61,961,244 ASPH, MIR4470, 5 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv4162573copy number variation1nstd166human GRCh37.p13 chr8: 62,788,878-62,863,191 , GRCh38.p12 chr8: 61,876,319-61,950,632 LINC02842, C1GALT1P3, 1 more genes
    nsv3924415copy number variation1nstd102humanPathogenic GRCh37 chr8: 61,431,781-67,571,260 , GRCh38 chr8: 60,519,222-66,659,025 , NCBI36 chr8: 61,594,335-67,733,814 RN7SKP135, TRIM55, 77 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3922631copy number variation1nstd102humanPathogenic GRCh38 chr8: 61,691,800-82,537,696 , NCBI36 chr8: 62,766,913-83,612,486 , GRCh37 chr8: 62,604,359-83,449,931 NCOA2, LOC107986893, 284 more genes
    nsv3919860copy number variation1nstd102humanUncertain significance NCBI36 chr8: 62,499,259-63,077,116 , GRCh37 chr8: 62,336,705-62,914,562 , GRCh38 chr8: 61,424,146-62,002,003 CLVS1, LINC02155, 7 more genes
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