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Items: 14

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    Number of Variants: 14

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 STT3B, LOC102724104, 291 more genes
    nsv3913369copy number variation1nstd102humanPathogenic NCBI36 chr3: 29,206,432-35,025,542 , GRCh37.p13 chr3: 29,231,428-35,050,538 , GRCh38.p12 chr3: 29,189,937-35,009,046 STT3B, MTND4LP9, 61 more genes
    nsv3882929copy number variation1nstd102humanPathogenic GRCh37 chr3: 29,689,082-34,233,218 , GRCh38.p12 chr3: 29,647,591-34,191,726 STT3B, MIR548AY, 56 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 STT3B, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 STT3B, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 STT3B, RPL23AP49, 2875 more genes
    nsv3905127copy number variation1nstd102humanPathogenic GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521 STT3B, LINC02022, 540 more genes
    nsv3876280copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-37,459,464 , GRCh38.p12 chr3: 20,213-37,417,973 STT3B, OXTR, 460 more genes
    nsv3892895copy number variation1nstd102humanPathogenic GRCh38 chr3: 52,266-37,148,076 , GRCh37 chr3: 93,949-37,189,567 , NCBI36 chr3: 68,949-37,164,571 STT3B, RPL34P11, 452 more genes
    nsv3878718copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-36,710,181 , GRCh38.p12 chr3: 20,213-36,668,690 STT3B, LRRC3B, 436 more genes
    nsv3875913copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-33,958,201 , GRCh38.p12 chr3: 20,213-33,916,709 STT3B, RPS27P11, 424 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 STT3B, RNU6-243P, 382 more genes
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 STT3B, RN7SL4P, 348 more genes
    nsv3888895copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 25,045,365-32,691,140 , GRCh38.p12 chr3: 25,003,874-32,649,648 STT3B, RARB, 83 more genes
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