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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5669930inversion1nstd207human GRCh38 chr16: 70,123,796-74,346,113 , GRCh37.p13 chr16: 70,157,699-74,380,011 , AARS1, 83 more genes
    nsv5557110sequence alteration1nstd206human GRCh38 chr16: 70,117,371-74,396,141 , GRCh37.p13 chr16: 70,151,274-74,430,039 , TAT, 84 more genes
    nsv5378447translocation1nstd200human GRCh38 chr6: 47,396,589-47,396,589 , GRCh38 chr16: 71,857,134-71,857,134 , GRCh37.p13 chr16: 71,891,037-71,891,037 , GRCh37.p13 chr6: 47,364,325-47,364,325 LOC105375082, ATXN1L
    nsv5341248translocation1nstd200human GRCh37 chr16: 71,891,037-71,891,037 , GRCh37 chr6: 47,364,325-47,364,325 , GRCh38.p12 chr16: 71,857,134-71,857,134 , GRCh38.p12 chr6: 47,396,589-47,396,589 LOC105375082, ATXN1L
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4993295copy number variation1nstd200human GRCh38 chr16: 71,841,163-71,844,215 , GRCh37.p13 chr16: 71,875,066-71,878,118 ATXN1L
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4759749inversion1nstd199human GRCh37 chr16: 70,151,143-74,397,976 , GRCh38.p12 chr16: 70,117,240-74,364,078 , AARS1, 85 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4675263copy number variation1nstd102humanUncertain significance GRCh37 chr16: 71,822,938-71,974,755 , GRCh38.p12 chr16: 71,789,035-71,940,852 PKD1L3, AP1G1, 4 more genes
    nsv4627092copy number variation1nstd183human GRCh37 chr16: 71,843,657-72,554,132 , GRCh38.p12 chr16: 71,809,754-72,520,233 LINC01572, LOC100420489, 14 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4377066copy number variation1nstd173human GRCh37 chr16: 70,197,501-72,654,326 , GRCh38.p12 chr16: 70,163,598-72,620,427 , LOC102725168, 67 more genes
    nsv4332560sequence alteration1nstd166human GRCh37.p13 chr16: 57,901,049-75,540,778 , GRCh38.p12 chr16: 57,867,145-75,506,880 , AGRP, 331 more genes
    nsv4321328inversion1nstd166human GRCh37.p13 chr16: 67,701,568-75,754,137 , GRCh38.p12 chr16: 67,667,665-75,720,239 , CDH3, 203 more genes
    nsv4236572copy number variation1nstd166human GRCh37.p13 chr16: 71,887,554-72,508,154 , GRCh38.p12 chr16: 71,853,651-72,474,255 TXNL4B, HPR, 13 more genes
    nsv3969586inversion1nstd168human GRCh38 chr16: 70,195,952-74,390,641 , GRCh37.p13 chr16: 70,229,855-74,424,539 , AARS1, 82 more genes
    nsv3922890copy number variation1nstd102humanPathogenic GRCh37 chr16: 70,783,301-90,163,403 , GRCh38 chr16: 70,749,398-90,096,995 , NCBI36 chr16: 69,340,802-88,690,904 GCSH, LOC390739, 362 more genes
    nsv3922616copy number variation1nstd102humanPathogenic GRCh38 chr16: 70,514,631-90,081,985 , NCBI36 chr16: 69,106,035-88,675,894 , GRCh37 chr16: 70,548,534-90,148,393 FOXF1, RNA5SP431, 367 more genes
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