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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965532insertion1nstd209human GRCh38 chr10: 95,677,473-95,677,473 , GRCh37.p13 chr10: 97,437,230-97,437,230 TCTN3
    nsv5925336copy number variation1nstd209human GRCh38 chr10: 95,662,003-95,662,074 , GRCh37.p13 chr10: 97,421,760-97,421,831 TCTN3
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5699541mobile element insertion1nstd211human GRCh38 chr10: 95,694,336-95,694,336 , GRCh37.p13 chr10: 97,454,093-97,454,093 TCTN3
    nsv5699295mobile element insertion1nstd211human GRCh38 chr10: 95,694,424-95,694,424 , GRCh37.p13 chr10: 97,454,181-97,454,181 TCTN3
    nsv5594866copy number variation1nstd207human GRCh38 chr10: 95,647,108-95,677,060 , GRCh37.p13 chr10: 97,406,865-97,436,817 ALDH18A1, TCTN3
    nsv5589939copy number variation1nstd207human GRCh38 chr10: 95,666,176-95,679,824 , GRCh37.p13 chr10: 97,425,933-97,439,581 TCTN3
    nsv5564286copy number variation1nstd102humanUncertain significance GRCh37 chr10: 97,366,499-98,031,175 , GRCh38.p12 chr10: 95,606,742-96,271,418 CCNJ, ENTPD1-AS1, 10 more genes
    nsv5492695copy number variation1nstd206human GRCh38 chr10: 95,647,108-95,677,058 , GRCh37.p13 chr10: 97,406,865-97,436,815 TCTN3, ALDH18A1
    nsv5479455copy number variation1nstd206human GRCh38 chr10: 95,666,126-95,679,801 , GRCh37.p13 chr10: 97,425,883-97,439,558 TCTN3
    nsv5410377mobile element insertion1nstd206human GRCh38 chr10: 95,694,336-95,694,387 , GRCh37.p13 chr10: 97,454,093-97,454,144 TCTN3
    nsv5309212copy number variation1nstd204human GRCh37.p13 chr10: 97,406,835-97,436,837 , GRCh38.p13 chr10: 95,647,078-95,677,080 ALDH18A1, TCTN3
    nsv5245308copy number variation1nstd204human GRCh38.p13 chr10: 95,646,908-95,675,456 , GRCh37.p13 chr10: 97,406,665-97,435,213 ALDH18A1, TCTN3
    nsv5135535mobile element insertion1nstd203human GRCh38 chr10: 95,680,932-95,680,952 , GRCh37.p13 chr10: 97,440,689-97,440,709 TCTN3
    nsv5134277mobile element insertion1nstd203human GRCh38 chr10: 95,677,474-95,677,501 , GRCh37.p13 chr10: 97,437,231-97,437,258 TCTN3
    nsv4986796copy number variation1nstd200human GRCh38 chr10: 95,666,226-95,679,804 , GRCh37.p13 chr10: 97,425,983-97,439,561 TCTN3
    nsv4986795copy number variation1nstd200human GRCh38 chr10: 95,647,108-95,677,058 , GRCh37.p13 chr10: 97,406,865-97,436,815 ALDH18A1, TCTN3
    nsv4847684copy number variation1nstd200human GRCh37 chr10: 97,425,942-97,439,602 , GRCh38.p12 chr10: 95,666,185-95,679,845 TCTN3
    nsv4839515copy number variation1nstd200human GRCh37 chr10: 97,406,865-97,436,815 , GRCh38.p12 chr10: 95,647,108-95,677,058 TCTN3, ALDH18A1
    nsv4729612copy number variation1nstd102humanUncertain significance GRCh37 chr10: 97,452,629-97,616,981 , GRCh38.p12 chr10: 95,692,872-95,857,224 TCTN3, ENTPD1, 1 more genes
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