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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5514038copy number variation1nstd206human GRCh38 chr18: 57,368,050-57,368,485 , GRCh37.p13 chr18: 55,035,281-55,035,716 ST8SIA3
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv4676235copy number variation1nstd102humanUncertain significance GRCh37 chr18: 54,552,231-55,285,563 , GRCh38.p12 chr18: 56,885,000-57,618,331 LOC105372136, WDR7-OT1, 9 more genes
    nsv4676212copy number variation1nstd102humanUncertain significance GRCh37 chr18: 54,652,730-55,528,259 , GRCh38.p12 chr18: 56,985,499-57,861,027 FECH, WDR7, 17 more genes
    nsv4676105copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240 MIR548AV, GTSCR1, 310 more genes
    nsv4665996copy number variation1nstd186human GRCh37 chr18: 55,018,801-55,021,300 , GRCh38.p12 chr18: 57,351,570-57,354,069 ST8SIA3
    nsv4631403copy number variation1nstd183human GRCh37 chr18: 55,018,801-55,021,300 , GRCh38.p12 chr18: 57,351,570-57,354,069 ST8SIA3
    nsv4531962copy number variation1nstd166human GRCh37.p13 chr18: 55,019,933-55,020,066 , GRCh38.p12 chr18: 57,352,702-57,352,835 ST8SIA3
    nsv4457866copy number variation1nstd102humanPathogenic GRCh37 chr18: 45,621,155-61,416,536 , GRCh38.p12 chr18: 48,094,784-63,749,302 LOC105372159, LOC105372156, 208 more genes
    nsv4457607copy number variation1nstd102humanUncertain significance GRCh37 chr18: 54,699,379-55,203,838 , GRCh38.p12 chr18: 57,032,148-57,536,606 RNU6-737P, LOC105372136, 6 more genes
    nsv4457604copy number variation1nstd102humanUncertain significance GRCh37 chr18: 54,583,962-55,296,715 , GRCh38.p12 chr18: 56,916,731-57,629,483 LOC105372136, WDR7-OT1, 10 more genes
    nsv4421136copy number variation1nstd174human GRCh37 chr18: 55,018,645-55,022,000 , GRCh38.p12 chr18: 57,351,414-57,354,769 ST8SIA3
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4320417inversion1nstd166human GRCh37.p13 chr18: 52,530,154-56,173,673 , GRCh38.p12 chr18: 54,862,923-58,506,441 , ONECUT2, 50 more genes
    nsv4262731copy number variation1nstd166human GRCh37.p13 chr18: 55,007,091-55,018,918 , GRCh38.p12 chr18: 57,339,860-57,351,687 ST8SIA3
    nsv4253299copy number variation1nstd166human GRCh37.p13 chr18: 54,533,639-55,332,520 , GRCh38.p12 chr18: 56,866,408-57,665,288 , BOD1L2, 12 more genes
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
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