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Items: 1 to 20 of 104

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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
    nsv6897339copy number variation1nstd229human GRCh38 chr10: 57,728,127-58,811,843 , GRCh37.p13 chr10: 59,487,887-60,571,603 CISD1, MRPS35P3, 9 more genes
    nsv6892084copy number variation1nstd229human GRCh38 chr10: 58,351,062-58,447,607 , GRCh37.p13 chr10: 60,110,822-60,207,367 TFAM, LOC105378316, 1 more genes
    nsv6888553copy number variation1nstd229human GRCh38 chr10: 52,267,558-58,421,311 , GRCh37.p13 chr10: 54,027,318-60,181,071 MRPS35P3, NEFMP1, 32 more genes
    nsv6887115copy number variation1nstd229human GRCh38 chr10: 58,397,093-58,398,261 , GRCh37.p13 chr10: 60,156,853-60,158,021 TFAM
    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
    nsv6879982copy number variation1nstd229human GRCh38 chr10: 58,351,172-58,392,962 , GRCh37.p13 chr10: 60,110,932-60,152,722 TFAM, UBE2D1
    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
    nsv6585869inversion1nstd223human GRCh38 chr10: 58,392,969-58,393,888 , GRCh37.p13 chr10: 60,152,729-60,153,648 TFAM
    nsv6584881inversion1nstd223human GRCh38 chr10: 54,170,455-58,863,076 , GRCh37.p13 chr10: 55,930,215-60,622,836 MIR548F1, LOC105378313, 20 more genes
    nsv5722355mobile element insertion2nstd211human GRCh38 chr10: 58,386,137-58,386,137 , GRCh37.p13 chr10: 60,145,897-60,145,897 TFAM
    nsv5558476mobile element insertion1nstd206human GRCh38 chr10: 58,386,137-58,386,188 , GRCh37.p13 chr10: 60,145,897-60,145,948 TFAM
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4729007copy number variation1nstd102humanLikely benign GRCh37 chr10: 60,151,412-60,583,505 , GRCh38.p12 chr10: 58,391,652-58,823,745 FAM133CP, BICC1, 2 more genes
    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
    nsv4615187copy number variation1nstd183human GRCh37 chr10: 60,154,614-60,155,529 , GRCh38.p12 chr10: 58,394,854-58,395,769 TFAM
    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
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