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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926913copy number variation1nstd209human GRCh38 chr11: 119,634,135-119,638,961 , GRCh37.p13 chr11: 119,504,846-119,509,671 LOC105369520, NECTIN1
    nsv5922829copy number variation1nstd209human GRCh38 chr11: 119,644,080-119,644,149 , GRCh37.p13 chr11: 119,514,790-119,514,859 NECTIN1
    nsv5922683copy number variation1nstd209human GRCh38 chr11: 119,649,333-119,652,480 , GRCh37.p13 chr11: 119,520,043-119,523,190 NECTIN1
    nsv5918881copy number variation1nstd209human GRCh38 chr11: 119,638,517-119,639,793 , GRCh37.p13 chr11: 119,509,227-119,510,503 NECTIN1, LOC105369520
    nsv5860543copy number variation1nstd209human GRCh38 chr11: 119,649,341-119,652,481 , GRCh37.p13 chr11: 119,520,051-119,523,191 NECTIN1
    nsv5853160copy number variation1nstd209human GRCh38 chr11: 119,634,103-119,639,002 , GRCh37.p13 chr11: 119,504,814-119,509,712 LOC105369520, NECTIN1
    nsv5659707insertion1nstd207human GRCh38 chr11: 119,648,412-119,648,412 , GRCh37.p13 chr11: 119,519,122-119,519,122 NECTIN1
    nsv5648330insertion1nstd207human GRCh38 chr11: 119,648,274-119,648,274 , GRCh37.p13 chr11: 119,518,984-119,518,984 NECTIN1
    nsv5648233insertion1nstd207human GRCh38 chr11: 119,648,349-119,648,349 , GRCh37.p13 chr11: 119,519,059-119,519,059 NECTIN1
    nsv5512218copy number variation1nstd206human GRCh38 chr11: 119,695,474-119,695,589 , GRCh37.p13 chr11: 119,566,184-119,566,299 NECTIN1
    nsv5504938copy number variation1nstd206human GRCh38 chr11: 119,634,142-119,638,962 , GRCh37.p13 chr11: 119,504,853-119,509,672 LOC105369520, NECTIN1
    nsv5499359copy number variation1nstd206human GRCh38 chr11: 119,649,333-119,652,481 , GRCh37.p13 chr11: 119,520,043-119,523,191 NECTIN1
    nsv5380954copy number variation1nstd102humanUncertain significance GRCh37 chr11: 119,077,108-120,133,495 , GRCh38.p12 chr11: 119,206,398-120,262,786 NECTIN1-DT, RNU6-262P, 29 more genes
    nsv5348355translocation1nstd200human GRCh38 chr11: 119,652,481-119,652,481 , GRCh38 chr11: 119,649,333-119,649,333 , GRCh37.p13 chr11: 119,520,043-119,520,043 , GRCh37.p13 chr11: 119,523,191-119,523,191 NECTIN1
    nsv5304345copy number variation1nstd204human GRCh37.p13 chr11: 119,504,830-119,509,701 , GRCh38.p13 chr11: 119,634,119-119,638,991 LOC105369520, NECTIN1
    nsv5276282copy number variation1nstd204human GRCh38.p13 chr11: 119,635,103-119,636,502 , GRCh37.p13 chr11: 119,505,813-119,507,212 NECTIN1, LOC105369520
    nsv5269038copy number variation1nstd204human GRCh38.p13 chr11: 119,634,003-119,639,002 , GRCh37.p13 chr11: 119,504,714-119,509,712 NECTIN1, LOC105369520
    nsv5266994copy number variation1nstd204human GRCh38.p13 chr11: 119,634,201-119,639,000 , GRCh37.p13 chr11: 119,504,912-119,509,710 LOC105369520, NECTIN1
    nsv4980980copy number variation1nstd200human GRCh38 chr11: 119,634,142-119,638,962 , GRCh37.p13 chr11: 119,504,853-119,509,672 LOC105369520, NECTIN1
    nsv4843743copy number variation1nstd200human GRCh37 chr11: 119,520,043-119,523,191 , GRCh38.p12 chr11: 119,649,333-119,652,481 NECTIN1
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