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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894852copy number variation1nstd209human GRCh38 chr3: 149,067,744-149,067,820 , GRCh37.p13 chr3: 148,785,531-148,785,607 HLTF
    nsv5683497mobile element insertion2nstd211human GRCh38 chr3: 149,040,174-149,040,174 , GRCh37.p13 chr3: 148,757,961-148,757,961 HLTF
    nsv5577706copy number variation1nstd207human GRCh38 chr3: 149,079,463-149,079,516 , GRCh37.p13 chr3: 148,797,250-148,797,303 HLTF
    nsv5571680copy number variation1nstd207human GRCh38 chr3: 149,067,744-149,067,820 , GRCh37.p13 chr3: 148,785,531-148,785,607 HLTF
    nsv5450471copy number variation1nstd206human GRCh38 chr3: 149,033,601-149,033,718 , GRCh37.p13 chr3: 148,751,388-148,751,505 HLTF
    nsv5448316copy number variation1nstd206human GRCh38 chr3: 149,067,744-149,067,815 , GRCh37.p13 chr3: 148,785,531-148,785,602 HLTF
    nsv5412814mobile element insertion1nstd206human GRCh38 chr3: 149,040,174-149,040,225 , GRCh37.p13 chr3: 148,757,961-148,758,012 HLTF
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5333811translocation1nstd200human GRCh37 chr3: 148,785,602-148,785,602 , GRCh37 chr3: 148,785,531-148,785,531 , GRCh38.p12 chr3: 149,067,815-149,067,815 , GRCh38.p12 chr3: 149,067,744-149,067,744 HLTF
    nsv5096541mobile element insertion1nstd203human GRCh38 chr3: 149,072,545-149,072,555 , GRCh37.p13 chr3: 148,790,332-148,790,342 HLTF
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4914882copy number variation1nstd200human GRCh38 chr3: 149,082,980-149,084,523 , GRCh37.p13 chr3: 148,800,767-148,802,310 HLTF, HLTF-AS1
    nsv4914881copy number variation1nstd200human GRCh38 chr3: 149,053,724-149,114,175 , GRCh37.p13 chr3: 148,771,511-148,831,962 MED28P2, HLTF-AS1, 1 more genes
    nsv4912308copy number variation1nstd200human GRCh38 chr3: 149,078,675-149,082,250 , GRCh37.p13 chr3: 148,796,462-148,800,037 HLTF
    nsv4804885copy number variation1nstd200human GRCh37 chr3: 148,800,767-148,802,312 , GRCh38.p12 chr3: 149,082,980-149,084,525 HLTF-AS1, HLTF
    nsv4791490copy number variation1nstd200human GRCh37 chr3: 148,796,462-148,800,037 , GRCh38.p12 chr3: 149,078,675-149,082,250 HLTF
    nsv4731825copy number variation1nstd199human GRCh37 chr3: 148,797,248-148,797,302 , GRCh38.p12 chr3: 149,079,461-149,079,515 HLTF
    nsv4708660copy number variation1nstd195human GRCh37 chr3: 148,504,301-148,814,451 , GRCh38.p12 chr3: 148,786,514-149,096,664 CPA3, CPB1, 6 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4674717copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 144,053,029-150,272,658 , GRCh38.p12 chr3: 144,334,187-150,554,871 AGTR1, CP, 83 more genes
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