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Items: 1 to 20 of 436

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5342855translocation1nstd200human GRCh37 chr19: 41,978,396-41,978,396 , GRCh37 chr19: 41,981,026-41,981,026 , GRCh38.p12 chr19|NT_187620.1: 215,224-215,224 , GRCh38.p12 chr19: 41,472,491-41,472,491 , GRCh38.p12 chr19: 41,475,119-41,475,119 , GRCh38.p12 chr19|NT_187620.1: 217,852-217,852 PCAT19
    nsv5335313translocation1nstd200human GRCh37 chr19: 42,168,566-42,168,566 , GRCh37 chr19: 42,169,036-42,169,036 , GRCh38.p12 chr19: 41,665,108-41,665,108 , GRCh38.p12 chr19|NT_187620.1: 16,893-16,893 , GRCh38.p12 chr19: 41,664,638-41,664,638 , GRCh38.p12 chr19|NT_187620.1: 17,363-17,363 LOC105372405
    nsv5333172translocation1nstd200human GRCh37 chr19: 42,086,655-42,086,655 , GRCh37 chr19: 42,086,748-42,086,748 , GRCh38.p12 chr19: 41,580,395-41,580,395 , GRCh38.p12 chr19|NT_187620.1: 101,699-101,699 , GRCh38.p12 chr19: 41,580,302-41,580,302 , GRCh38.p12 chr19|NT_187620.1: 101,606-101,606 CEACAM21
    nsv4868429copy number variation1nstd200human GRCh37 chr19: 42,167,231-42,167,925 , GRCh38.p12 chr19|NT_187620.1: 17,998-18,692 , GRCh38.p12 chr19: 41,663,303-41,663,997 LOC105372405
    nsv4868428copy number variation1nstd200human GRCh37 chr19: 42,149,115-42,150,047 , GRCh38.p12 chr19: 41,642,747-41,643,679 , GRCh38.p12 chr19|NT_187620.1: 38,322-39,254 LOC105372405
    nsv4868427copy number variation1nstd200human GRCh37 chr19: 42,117,133-42,119,158 , GRCh38.p12 chr19|NT_187620.1: 69,201-71,228 , GRCh38.p12 chr19: 41,610,773-41,612,800 0
    nsv4868426copy number variation1nstd200human GRCh37 chr19: 42,105,466-42,109,632 , GRCh38.p12 chr19|NT_187620.1: 78,726-82,892 , GRCh38.p12 chr19: 41,599,111-41,603,277 LOC105372404, CEACAMP3
    nsv4868425copy number variation1nstd200human GRCh37 chr19: 42,059,316-42,062,139 , GRCh38.p12 chr19: 41,552,946-41,555,769 , GRCh38.p12 chr19|NT_187620.1: 126,232-129,055 CEACAM21
    nsv4868424copy number variation1nstd200human GRCh37 chr19: 42,019,240-42,020,427 , GRCh38.p12 chr19: 41,512,867-41,514,054 , GRCh38.p12 chr19|NT_187620.1: 176,289-177,476 0
    nsv4868423copy number variation1nstd200human GRCh37 chr19: 42,017,711-42,020,051 , GRCh38.p12 chr19: 41,511,338-41,513,678 , GRCh38.p12 chr19|NT_187620.1: 176,665-179,005 0
    nsv4868422copy number variation1nstd200human GRCh37 chr19: 42,016,645-42,016,789 , GRCh38.p12 chr19|NT_187620.1: 179,927-180,071 , GRCh38.p12 chr19: 41,510,272-41,510,416 0
    nsv4868421copy number variation1nstd200human GRCh37 chr19: 42,012,609-42,012,971 , GRCh38.p12 chr19|NT_187620.1: 183,288-183,650 , GRCh38.p12 chr19: 41,506,693-41,507,055 TPM3P5
    nsv4868420copy number variation1nstd200human GRCh37 chr19: 42,002,627-42,010,609 , GRCh38.p12 chr19: 41,496,717-41,504,693 , GRCh38.p12 chr19|NT_187620.1: 185,650-193,626 TPM3P5, PCAT19
    nsv4868419copy number variation1nstd200human GRCh37 chr19: 41,973,521-41,974,079 , GRCh38.p12 chr19: 41,467,616-41,468,174 , GRCh38.p12 chr19|NT_187620.1: 222,169-222,727 PCAT19
    nsv4868418copy number variation1nstd200human GRCh37 chr19: 41,972,642-42,008,216 , GRCh38.p12 chr19: 41,466,737-41,502,300 , GRCh38.p12 chr19|NT_187620.1: 188,043-223,606 PCAT19
    nsv4868417copy number variation1nstd200human GRCh37 chr19: 41,966,814-41,967,906 , GRCh38.p12 chr19|NT_187620.1: 228,343-229,435 , GRCh38.p12 chr19: 41,460,908-41,462,000 PCAT19
    nsv4738875copy number variation1nstd199human GRCh37 chr19: 42,129,215-42,129,267 , GRCh38.p12 chr19|NT_187620.1: 59,107-59,159 , GRCh38.p12 chr19: 41,622,842-41,622,890 CEACAM4
    nsv4707480copy number variation1nstd195human GRCh37 chr19: 41,958,201-41,993,901 , GRCh38.p12 chr19: 41,452,296-41,487,993 , GRCh38.p12 chr19|NT_187620.1: 202,350-233,762 PCAT19
    nsv4702641copy number variation1nstd195human GRCh37 chr19: 41,998,201-42,367,401 , GRCh38.p12 chr19: 41,492,293-41,863,329 , GRCh38.p12 chr19|NT_187620.1: 1-198,050 CEACAM5, CEACAM7, 20 more genes
    nsv4676231copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,889,319-42,338,832 , GRCh38.p12 chr19: 41,383,414-41,834,777 , GRCh38.p12 chr19|NT_187620.1: 1-233,762 CEACAM7, LYPD4, 25 more genes
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