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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5659873insertion1nstd207human GRCh38 chr16: 67,980,874-67,980,874 , GRCh37.p13 chr16: 68,014,777-68,014,777 DPEP3
    nsv5525144copy number variation1nstd206human GRCh38 chr16: 67,934,595-68,008,992 , GRCh37.p13 chr16: 67,968,498-68,042,895 LCAT, PSMB10, 4 more genes
    nsv5365684translocation1nstd200human GRCh38 chr16: 67,978,858-67,978,858 , GRCh38 chr16: 67,978,685-67,978,685 , GRCh37.p13 chr16: 68,012,588-68,012,588 , GRCh37.p13 chr16: 68,012,761-68,012,761 DPEP3
    nsv5334292translocation1nstd200human GRCh37 chr16: 68,012,588-68,012,588 , GRCh37 chr16: 68,012,761-68,012,761 , GRCh38.p12 chr16: 67,978,685-67,978,685 , GRCh38.p12 chr16: 67,978,858-67,978,858 DPEP3
    nsv5272913copy number variation1nstd204human GRCh38.p13 chr16: 67,454,801-68,159,500 , GRCh37.p13 chr16: 67,488,704-68,193,403 EDC4, ATP6V0D1, 31 more genes
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4993131copy number variation1nstd200human GRCh38 chr16: 67,973,213-67,978,857 , GRCh37.p13 chr16: 68,007,116-68,012,760 DPEP3
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4857498copy number variation1nstd200human GRCh37 chr16: 68,007,116-68,012,760 , GRCh38.p12 chr16: 67,973,213-67,978,857 DPEP3
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729756copy number variation1nstd102humanUncertain significance GRCh37 chr16: 67,765,964-68,246,270 , GRCh38.p12 chr16: 67,732,061-68,212,367 DUS2, RNU6-359P, 19 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
    nsv4675201copy number variation1nstd102humanPathogenic GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280 LOC100420066, LINC00920, 143 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
    nsv4350223copy number variation1nstd102humanPathogenic GRCh37 chr16: 67,132,790-68,166,320 , GRCh38.p12 chr16: 67,098,887-68,132,417 CBFB, B3GNT9, 55 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
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv3920399copy number variation1nstd102humanPathogenic NCBI36 chr16: 61,517,334-83,176,902 , GRCh37 chr16: 62,959,833-84,619,401 , GRCh38 chr16: 62,925,929-84,585,795 LOC654780, LSM3P5, 385 more genes
    nsv3919817copy number variation1nstd102humanPathogenic NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985 LOC105376772, WWP2, 527 more genes
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