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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944632copy number variation1nstd209human GRCh38 chr19: 56,622,034-56,622,117 , GRCh37.p13 chr19: 57,133,402-57,133,485 ZNF71, ZNF71-SMIM17
    nsv5929787copy number variation1nstd209human GRCh38 chr19: 56,600,176-56,600,493 , GRCh37.p13 chr19: 57,111,544-57,111,861 ZNF71, ZNF71-SMIM17
    nsv5928453copy number variation1nstd209human GRCh38 chr19: 56,611,440-56,611,502 , GRCh37.p13 chr19: 57,122,808-57,122,870 ZNF71, ZNF71-SMIM17
    nsv5705579mobile element insertion1nstd211human GRCh38 chr19: 56,608,276-56,608,276 , GRCh37.p13 chr19: 57,119,644-57,119,644 ZNF71-SMIM17, ZNF71
    nsv5589841copy number variation1nstd207human GRCh38 chr19: 56,609,617-56,609,757 , GRCh37.p13 chr19: 57,120,985-57,121,125 ZNF71, ZNF71-SMIM17
    nsv5586716copy number variation1nstd207human GRCh38 chr19: 56,600,176-56,600,493 , GRCh37.p13 chr19: 57,111,544-57,111,861 ZNF71, ZNF71-SMIM17
    nsv5530171copy number variation1nstd206human GRCh38 chr19: 56,622,409-56,622,661 , GRCh37.p13 chr19: 57,133,777-57,134,029 ZNF71-SMIM17, ZNF71
    nsv5525369copy number variation1nstd206human GRCh38 chr19: 56,600,192-56,600,494 , GRCh37.p13 chr19: 57,111,560-57,111,862 ZNF71, ZNF71-SMIM17
    nsv5416888mobile element insertion1nstd206human GRCh38 chr19: 56,608,276-56,608,327 , GRCh37.p13 chr19: 57,119,644-57,119,695 ZNF71-SMIM17, ZNF71
    nsv5385134mobile element deletion2nstd186human GRCh37 chr19: 57,111,560-57,111,862 , GRCh38.p12 chr19: 56,600,192-56,600,494 ZNF71-SMIM17, ZNF71
    nsv5359961translocation1nstd200human GRCh38 chr19: 56,611,503-56,611,503 , GRCh38 chr19: 56,611,441-56,611,441 , GRCh37.p13 chr19: 57,122,871-57,122,871 , GRCh37.p13 chr19: 57,122,809-57,122,809 ZNF71-SMIM17, ZNF71
    nsv5343869translocation1nstd200human GRCh37 chr19: 57,122,871-57,122,871 , GRCh37 chr19: 57,122,809-57,122,809 , GRCh38.p12 chr19: 56,611,441-56,611,441 , GRCh38.p12 chr19: 56,611,503-56,611,503 ZNF71-SMIM17, ZNF71
    nsv5300138copy number variation1nstd204human GRCh38.p13 chr19: 56,600,201-56,600,500 , GRCh37.p13 chr19: 57,111,569-57,111,868 ZNF71-SMIM17, ZNF71
    nsv5212430mobile element deletion1nstd204human GRCh37.p13 chr19: 57,111,560-57,111,862 , GRCh38.p13 chr19: 56,600,192-56,600,494 ZNF71-SMIM17, ZNF71
    nsv5176281mobile element insertion1nstd203human GRCh38 chr19: 56,608,265-56,608,276 , GRCh37.p13 chr19: 57,119,633-57,119,644 ZNF71, ZNF71-SMIM17
    nsv5028149copy number variation1nstd200human GRCh38 chr19: 56,622,221-56,622,274 , GRCh37.p13 chr19: 57,133,589-57,133,642 ZNF71-SMIM17, ZNF71
    nsv5028148copy number variation1nstd200human GRCh38 chr19: 56,621,703-56,622,352 , GRCh37.p13 chr19: 57,133,071-57,133,720 ZNF71, ZNF71-SMIM17
    nsv5024993copy number variation1nstd200human GRCh38 chr19: 56,620,588-56,656,263 , GRCh37.p13 chr19: 57,131,956-57,167,631 ZNF71-SMIM17, SMIM17, 1 more genes
    nsv5024990copy number variation1nstd200human GRCh38 chr19: 56,281,268-56,763,071 , GRCh37.p13 chr19: 56,792,637-57,274,439 , ZNF667-AS1, 28 more genes
    nsv4907575mobile element deletion1nstd200human GRCh38 chr19: 56,600,192-56,600,494 , GRCh37.p13 chr19: 57,111,560-57,111,862 ZNF71-SMIM17, ZNF71
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