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Items: 1 to 20 of 845

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972880insertion1nstd209human GRCh38 chr18: 7,021,794-7,021,794 , GRCh37.p13 chr18: 7,021,793-7,021,793 LAMA1
    nsv5945598copy number variation1nstd209human GRCh38 chr18: 7,073,837-7,073,889 , GRCh37.p13 chr18: 7,073,836-7,073,888 LAMA1
    nsv5941487copy number variation1nstd209human GRCh38 chr18: 7,082,885-7,082,967 , GRCh37.p13 chr18: 7,082,884-7,082,966 LAMA1
    nsv5939161copy number variation1nstd209human GRCh38 chr18: 7,107,757-7,108,079 , GRCh37.p13 chr18: 7,107,756-7,108,078 LAMA1
    nsv5932538copy number variation1nstd209human GRCh38 chr18: 7,038,204-7,038,262 , GRCh37.p13 chr18: 7,038,203-7,038,261 LAMA1
    nsv5869304copy number variation1nstd209human GRCh38 chr18: 7,077,445-7,078,596 , GRCh37.p13 chr18: 7,077,444-7,078,595 LAMA1
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5662137insertion1nstd207human GRCh38 chr18: 6,952,954-6,952,954 , GRCh37.p13 chr18: 6,952,953-6,952,953 LAMA1, LOC101927188
    nsv5653061insertion1nstd207human GRCh38 chr18: 7,021,794-7,021,794 , GRCh37.p13 chr18: 7,021,793-7,021,793 LAMA1
    nsv5649525insertion1nstd207human GRCh38 chr18: 6,952,910-6,952,910 , GRCh37.p13 chr18: 6,952,909-6,952,909 LAMA1, LOC101927188
    nsv5601864copy number variation1nstd207human GRCh38 chr18: 7,073,837-7,073,889 , GRCh37.p13 chr18: 7,073,836-7,073,888 LAMA1
    nsv5597778copy number variation1nstd207human GRCh38 chr18: 7,082,885-7,082,967 , GRCh37.p13 chr18: 7,082,884-7,082,966 LAMA1
    nsv5586777copy number variation1nstd207human GRCh38 chr18: 7,098,703-7,098,828 , GRCh37.p13 chr18: 7,098,702-7,098,827 LAMA1
    nsv5533142copy number variation1nstd206human GRCh38 chr18: 7,082,885-7,082,968 , GRCh37.p13 chr18: 7,082,884-7,082,967 LAMA1
    nsv5532256copy number variation1nstd206human GRCh38 chr18: 7,053,783-7,053,854 , GRCh37.p13 chr18: 7,053,782-7,053,853 LAMA1
    nsv5532166copy number variation1nstd206human GRCh38 chr18: 7,021,803-7,021,853 , GRCh37.p13 chr18: 7,021,802-7,021,852 LAMA1
    nsv5531540copy number variation1nstd206human GRCh38 chr18: 6,967,788-6,967,863 , GRCh37.p13 chr18: 6,967,787-6,967,862 LAMA1
    nsv5527842copy number variation1nstd206human GRCh38 chr18: 6,947,058-6,947,112 , GRCh37.p13 chr18: 6,947,057-6,947,111 LAMA1
    nsv5527121copy number variation1nstd206human GRCh38 chr18: 7,117,944-7,118,021 , GRCh37.p13 chr18: 7,117,943-7,118,020 LAMA1
    nsv5524718copy number variation1nstd206human GRCh38 chr18: 6,921,566-7,069,107 , GRCh37.p13 chr18: 6,921,565-7,069,106 RNU6-916P, LAMA1, 3 more genes
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