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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5527942copy number variation1nstd206human GRCh38 chr19: 35,659,678-35,665,978 , GRCh37.p13 chr19: 36,150,580-36,156,880 UPK1A, UPK1A-AS1
    nsv5522588copy number variation1nstd206human GRCh38 chr19: 35,675,498-35,716,472 , GRCh37.p13 chr19: 36,166,400-36,207,374 ZBTB32, TYMSP2, 2 more genes
    nsv5515925copy number variation1nstd206human GRCh38 chr19: 35,671,268-35,671,421 , GRCh37.p13 chr19: 36,162,170-36,162,323 UPK1A, UPK1A-AS1
    nsv5514799copy number variation1nstd206human GRCh38 chr19: 35,660,728-35,669,477 , GRCh37.p13 chr19: 36,151,630-36,160,379 UPK1A-AS1, UPK1A
    nsv5359751translocation1nstd200human GRCh38 chr19: 35,669,477-35,669,477 , GRCh38 chr19: 35,660,728-35,660,728 , GRCh37.p13 chr19: 36,160,379-36,160,379 , GRCh37.p13 chr19: 36,151,630-36,151,630 UPK1A-AS1, UPK1A
    nsv5166484mobile element insertion1nstd203human GRCh38 chr19: 35,672,588-35,672,596 , GRCh37.p13 chr19: 36,163,490-36,163,498 UPK1A, UPK1A-AS1
    nsv5024569copy number variation1nstd200human GRCh38 chr19: 35,675,405-35,716,472 , GRCh37.p13 chr19: 36,166,307-36,207,374 ZBTB32, TYMSP2, 2 more genes
    nsv4868183copy number variation1nstd200human GRCh37 chr19: 36,151,630-36,160,379 , GRCh38.p12 chr19: 35,660,728-35,669,477 UPK1A, UPK1A-AS1
    nsv4865132copy number variation1nstd200human GRCh37 chr19: 36,166,307-36,207,374 , GRCh38.p12 chr19: 35,675,405-35,716,472 TYMSP2, UPK1A, 2 more genes
    nsv4748875copy number variation1nstd199human GRCh37 chr19: 36,162,120-36,162,231 , GRCh38.p12 chr19: 35,671,218-35,671,329 UPK1A, UPK1A-AS1
    nsv4674329copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397 LOC105372379, LSR, 50 more genes
    nsv4629155copy number variation1nstd183human GRCh37 chr19: 36,157,771-36,159,732 , GRCh38.p12 chr19: 35,666,869-35,668,830 UPK1A-AS1, UPK1A
    nsv4624007copy number variation1nstd183human GRCh37 chr19: 36,151,606-36,160,333 , GRCh38.p12 chr19: 35,660,704-35,669,431 UPK1A-AS1, UPK1A
    nsv4457800copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,613,953-36,183,886 , GRCh38.p12 chr19: 35,123,049-35,692,984 SBSN, UPK1A, 38 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4429500copy number variation1nstd174human GRCh37 chr19: 36,151,588-36,160,400 , GRCh38.p12 chr19: 35,660,686-35,669,498 UPK1A-AS1, UPK1A
    nsv4350190copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742 SCN1B, ETV2, 76 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv4268443copy number variation1nstd166human GRCh37.p13 chr19: 36,166,307-36,207,363 , GRCh38.p12 chr19: 35,675,405-35,716,461 TYMSP2, KMT2B, 2 more genes
    nsv4262048copy number variation1nstd166human GRCh37.p13 chr19: 36,162,190-36,162,303 , GRCh38.p12 chr19: 35,671,288-35,671,401 UPK1A-AS1, UPK1A
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