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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv6893453copy number variation1nstd229human GRCh38 chr10: 58,997,288-58,997,644 , GRCh37.p13 chr10: 60,757,048-60,757,404 LINC00844
    nsv6889453copy number variation1nstd229human GRCh38 chr10: 58,821,063-59,002,216 , GRCh37.p13 chr10: 60,580,823-60,761,976 LINC00844, BICC1, 1 more genes
    nsv6885617copy number variation1nstd229human GRCh38 chr10: 58,984,901-59,018,000 , GRCh37.p13 chr10: 60,744,661-60,777,760 LOC102724768, LINC00844
    nsv6884001copy number variation1nstd229human GRCh38 chr10: 57,418,641-61,973,578 , GRCh37.p13 chr10: 59,178,401-63,733,337 LINC02625, ARID5B, 40 more genes
    nsv6637363copy number variation1nstd102humanUncertain significance GRCh37 chr10: 57,941,252-64,846,332 , GRCh38.p12 chr10: 56,181,491-63,086,572 TMEM26-AS1, LOC112268068, 53 more genes
    nsv6452881copy number variation1nstd223human GRCh38 chr10: 58,997,288-58,997,644 , GRCh37.p13 chr10: 60,757,048-60,757,404 LINC00844
    nsv6131794copy number variation1nstd213human GRCh37 chr10: 60,620,000-60,890,001 , GRCh38.p12 chr10: 58,860,240-59,130,241 RPLP1P10, LINC00844, 2 more genes
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4973681copy number variation1nstd200human GRCh38 chr10: 58,997,288-58,997,645 , GRCh37.p13 chr10: 60,757,048-60,757,405 LINC00844
    nsv4842634copy number variation1nstd200human GRCh37 chr10: 60,757,048-60,757,405 , GRCh38.p12 chr10: 58,997,288-58,997,645 LINC00844
    nsv4675795copy number variation1nstd102humanPathogenic GRCh37 chr10: 55,589,950-63,990,649 , GRCh38.p12 chr10: 53,830,190-62,230,890 ARL4AP1, CABCOCO1, 52 more genes
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
    nsv4675436copy number variation1nstd102humanPathogenic GRCh37 chr10: 56,031,210-65,660,398 , GRCh38.p12 chr10: 54,271,450-63,900,638 MRPL35P2, MIR1296, 77 more genes
    nsv4674846copy number variation1nstd102humanUncertain significance GRCh37 chr10: 60,327,012-60,814,229 , GRCh38.p12 chr10: 58,567,252-59,054,469 FAM133CP, BICC1, 3 more genes
    nsv4455623copy number variation1nstd102humanUncertain significance GRCh37 chr10: 59,199,424-62,981,900 , GRCh38.p12 chr10: 57,439,664-61,222,142 FAM133CP, IPMK, 35 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 more genes
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