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Items: 1 to 20 of 203

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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
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4599471copy number variation1nstd183human GRCh37 chr10: 94,449,208-94,450,485 , GRCh38.p12 chr10: 92,689,451-92,690,728 HHEX
    nsv4416861copy number variation1nstd174human GRCh37 chr10: 94,449,208-94,450,485 , GRCh38.p12 chr10: 92,689,451-92,690,728 HHEX
    nsv4348834copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 94,393,383-97,219,175 , GRCh38.p12 chr10: 92,633,626-95,459,418 CYP2C19, CYP2C8, 51 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
    nsv3914138copy number variation1nstd102humanPathogenic GRCh37 chr10: 94,403,676-97,230,894 , GRCh38 chr10: 92,643,919-95,471,137 , NCBI36 chr10: 94,393,656-97,220,884 RPL7AP52, LGI1, 51 more genes
    nsv3912487copy number variation1nstd102humanPathogenic GRCh37 chr10: 94,386,437-99,514,859 , GRCh38 chr10: 92,626,680-97,755,102 , NCBI36 chr10: 94,376,417-99,504,849 ENTPD1-AS1, PLCE1, 105 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
    nsv3905489copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639 LOC105378476, SMC3, 688 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    nsv3901659copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,186,527-95,820,286 , GRCh38.p12 chr10: 91,426,770-94,060,529 NHP2P1, SRP9P1, 48 more genes
    nsv3901597copy number variation1nstd102humanBenign GRCh37 chr10: 94,429,526-94,452,430 , GRCh38.p12 chr10: 92,669,769-92,692,673 EIF2S2P3, HHEX
    nsv3897772copy number variation1nstd102humanBenign GRCh37 chr10: 94,449,340-94,450,334 , GRCh38.p12 chr10: 92,689,583-92,690,577 HHEX
    nsv3894877copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,908,171-101,809,723 , GRCh38.p12 chr10: 92,148,414-100,049,966 RNY3P12, ANKRD2, 146 more genes
    nsv3894666copy number variation1nstd102humanBenign GRCh37 chr10: 94,449,340-94,449,749 , GRCh38.p12 chr10: 92,689,583-92,689,992 HHEX
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