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Items: 1 to 20 of 103

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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
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7066197inversion1nstd229human GRCh38 chr10: 90,423,055-91,029,089 , GRCh37.p13 chr10: 92,182,812-92,788,846 RPP30, HTR7, 5 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6896426copy number variation1nstd229human GRCh38 chr10: 90,912,976-90,915,541 , GRCh37.p13 chr10: 92,672,733-92,675,298 ANKRD1
    nsv6890617copy number variation1nstd229human GRCh38 chr10: 90,906,010-90,916,604 , GRCh37.p13 chr10: 92,665,767-92,676,361 ANKRD1, RPP30
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6131984copy number variation1nstd213human GRCh37 chr10: 92,240,000-92,800,001 , GRCh38.p12 chr10: 90,480,243-91,040,244 HTR7, RPP30, 6 more genes
    nsv5538971insertion1nstd206human GRCh38 chr10: 90,919,005-90,919,037 , GRCh37.p13 chr10: 92,678,762-92,678,794 ANKRD1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4675983copy number variation1nstd102humanUncertain significance GRCh37 chr10: 92,614,401-92,722,894 , GRCh38.p12 chr10: 90,854,644-90,963,137 HTR7, XLOC_008559, 3 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
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3908115copy number variation1nstd102humanPathogenic GRCh37 chr10: 92,667,881-98,970,384 , GRCh38.p12 chr10: 90,908,124-97,210,627 EXOC6, MARCHF5, 118 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 SHOC2, FAM245B, 1487 more genes
    nsv3906886copy number variation1nstd102humanUncertain significance GRCh37 chr10: 92,605,118-92,926,773 , GRCh38.p12 chr10: 90,845,361-91,167,016 LOC105378429, RPP30, 10 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
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