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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5695963mobile element insertion1nstd211human GRCh38 chr10: 91,790,649-91,790,649 , GRCh37.p13 chr10: 93,550,406-93,550,406 TNKS2-DT
    nsv5487734copy number variation1nstd206human GRCh38 chr10: 91,792,631-91,794,149 , GRCh37.p13 chr10: 93,552,388-93,553,906 TNKS2-DT
    nsv5305158copy number variation1nstd204human GRCh38.p13 chr10: 91,792,620-91,794,158 , GRCh37.p13 chr10: 93,552,377-93,553,915 TNKS2-DT
    nsv5248873copy number variation1nstd204human GRCh38.p13 chr10: 91,792,685-91,794,134 , GRCh37.p13 chr10: 93,552,442-93,553,891 TNKS2-DT
    nsv5193705mobile element insertion1nstd203human GRCh38 chr10: 91,795,560-91,795,572 , GRCh37.p13 chr10: 93,555,317-93,555,329 TNKS2-DT
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986641copy number variation1nstd200human GRCh38 chr10: 91,795,826-91,796,136 , GRCh37.p13 chr10: 93,555,583-93,555,893 TNKS2-DT
    nsv4986640copy number variation1nstd200human GRCh38 chr10: 91,792,619-91,794,152 , GRCh37.p13 chr10: 93,552,376-93,553,909 TNKS2-DT
    nsv4846663copy number variation1nstd200human GRCh37 chr10: 93,552,378-93,553,916 , GRCh38.p12 chr10: 91,792,621-91,794,159 TNKS2-DT
    nsv4540528insertion1nstd166human GRCh37.p13 chr10: 93,555,317-93,555,317 , GRCh38.p12 chr10: 91,795,560-91,795,560 TNKS2-DT
    nsv4488231mobile element insertion1nstd166human GRCh37.p13 chr10: 93,550,797-93,550,797 , GRCh38.p12 chr10: 91,791,040-91,791,040 TNKS2-DT
    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
    nsv4185897copy number variation1nstd166human GRCh37.p13 chr10: 93,552,408-93,553,886 , GRCh38.p12 chr10: 91,792,651-91,794,129 TNKS2-DT
    nsv4178258copy number variation1nstd166human GRCh37.p13 chr10: 93,555,583-93,555,893 , GRCh38.p12 chr10: 91,795,826-91,796,136 TNKS2-DT
    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
    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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