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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943763copy number variation1nstd209human GRCh38 chr19: 54,872,962-54,876,907 , GRCh37.p13 chr19|NW_004166865.1: 847,330-851,275 FCAR
    nsv5879015copy number variation1nstd209human GRCh38 chr19: 54,873,056-54,876,950 , GRCh37.p13 chr19|NW_004166865.1: 847,424-851,318 FCAR
    nsv5868536copy number variation1nstd209human GRCh38 chr19: 54,875,001-54,876,700 , GRCh37.p13 chr19|NW_004166865.1: 849,369-851,068 FCAR
    nsv5867771copy number variation1nstd209human GRCh38 chr19: 54,872,956-54,875,100 , GRCh37.p13 chr19|NW_004166865.1: 847,324-849,468 FCAR
    nsv5651108insertion1nstd207human GRCh38 chr19: 54,887,365-54,887,365 , GRCh37.p13 chr19|NW_004166865.1: 861,733-861,733 FCAR
    nsv5562501mobile element insertion1nstd206human GRCh38 chr19: 54,881,375-54,881,394 , GRCh37.p13 chr19|NW_004166865.1: 855,743-855,762 FCAR
    nsv5524233copy number variation1nstd206human GRCh38 chr19: 54,834,874-54,879,000 , GRCh37.p13 chr19|NW_004166865.1: 809,242-853,368 FCAR, KIR3DL2, 2 more genes
    nsv5380324translocation1nstd200human GRCh38 chr19: 54,881,375-54,881,375 , GRCh38 chr19: 54,880,552-54,880,552 , GRCh37.p13 chr19|NW_004166865.1: 854,920-854,920 , GRCh37.p13 chr19|NW_004166865.1: 855,743-855,743 FCAR
    nsv5380323translocation1nstd200human GRCh38 chr19: 54,880,375-54,880,375 , GRCh38 chr19: 54,881,395-54,881,395 , GRCh37.p13 chr19|NW_004166865.1: 854,743-854,743 , GRCh37.p13 chr19|NW_004166865.1: 855,763-855,763 FCAR
    nsv5359944translocation1nstd200human GRCh38 chr19: 54,886,629-54,886,629 , GRCh38 chr19: 54,962,862-54,962,862 , GRCh37.p13 chr19|NW_004166865.1: 860,997-860,997 , GRCh37.p13 chr19|NW_004166865.1: 937,230-937,230 NLRP7, FCAR
    nsv5332720translocation1nstd200human GRCh37 chr19: 55,392,008-55,392,008 , GRCh37 chr19: 55,392,831-55,392,831 , GRCh38.p12 chr19|NT_187693.1: 863,122-863,122 , GRCh38.p12 chr19|NT_187693.1: 863,945-863,945 FCAR
    nsv5331855translocation1nstd200human GRCh37 chr19: 55,392,851-55,392,851 , GRCh37 chr19: 55,391,831-55,391,831 , GRCh38.p12 chr19|NT_187693.1: 862,945-862,945 , GRCh38.p12 chr19|NT_187693.1: 863,965-863,965 FCAR
    nsv5326012translocation1nstd204human GRCh38.p13 chr19: 54,880,552-54,880,552 , GRCh38.p13 chr19: 54,881,375-54,881,375 , GRCh37.p13 chr19|NW_004166865.1: 854,920-854,920 , GRCh37.p13 chr19|NW_004166865.1: 855,743-855,743 FCAR
    nsv5321907translocation1nstd204human GRCh38.p13 chr19: 54,880,375-54,880,375 , GRCh38.p13 chr19: 54,881,395-54,881,395 , GRCh37.p13 chr19|NW_004166865.1: 854,743-854,743 , GRCh37.p13 chr19|NW_004166865.1: 855,763-855,763 FCAR
    nsv5192586mobile element insertion1nstd203human GRCh38 chr19: 54,872,276-54,872,289 , GRCh37.p13 chr19|NW_004166865.1: 846,644-846,657 FCAR
    nsv5028040copy number variation1nstd200human GRCh38 chr19: 54,887,921-54,889,305 , GRCh37.p13 chr19|NW_004166865.1: 862,289-863,673 FCAR
    nsv5028039copy number variation1nstd200human GRCh38 chr19: 54,886,199-54,945,193 , GRCh37.p13 chr19|NW_004166865.1: 860,567-919,561 FCAR, NLRP7, 1 more genes
    nsv5028038copy number variation1nstd200human GRCh38 chr19: 54,882,264-54,882,382 , GRCh37.p13 chr19|NW_004166865.1: 856,632-856,750 FCAR
    nsv4861364copy number variation1nstd200human GRCh37 chr19: 55,399,288-55,400,672 , GRCh38.p12 chr19|NT_187693.1: 870,402-871,786 FCAR
    nsv4861363copy number variation1nstd200human GRCh37 chr19: 55,397,611-55,456,573 , GRCh38.p12 chr19: 54,911,984-54,945,205 , GRCh38.p12 chr19|NW_003571060.1: 790,564-849,562 , GRCh38.p12 chr19|NW_003571058.2: 879,326-927,277 , GRCh38.p12 chr19|NT_187693.1: 894,466-927,687 , GRCh38.p12 chr19|NW_003571061.2: 609,415-657,366 , GRCh38.p12 chr19|NW_003571057.2: 904,777-952,728 , GRCh38.p12 chr19|NW_003571059.2: 815,619-863,570 , GRCh38.p12 chr19|NW_003571056.2: 877,240-925,191 , GRCh38.p12 chr19|NW_003571055.2: 531,431-590,407 , GRCh38.p12 chr19|NW_003571054.1: 800,652-848,603 FCAR, NCR1, 1 more genes
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