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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5913806copy number variation1nstd209human GRCh38 chr7: 139,522,401-139,522,715 , GRCh37.p13 chr7: 139,207,147-139,207,461 CLEC2L
    nsv5634414insertion1nstd207human GRCh38 chr7: 139,543,222-139,543,222 , GRCh37.p13 chr7: 139,227,968-139,227,968 CLEC2L
    nsv5570933copy number variation1nstd207human GRCh38 chr7: 139,522,401-139,522,715 , GRCh37.p13 chr7: 139,207,147-139,207,461 CLEC2L
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5485624copy number variation1nstd206human GRCh38 chr7: 139,536,693-139,538,197 , GRCh37.p13 chr7: 139,221,439-139,222,943 CLEC2L
    nsv5477775copy number variation1nstd206human GRCh38 chr7: 139,522,415-139,522,716 , GRCh37.p13 chr7: 139,207,161-139,207,462 CLEC2L
    nsv5384603mobile element deletion2nstd186human GRCh37 chr7: 139,207,161-139,207,462 , GRCh38.p12 chr7: 139,522,415-139,522,716 CLEC2L
    nsv5361897translocation1nstd200human GRCh38 chr3: 123,559,016-123,559,016 , GRCh38 chr7: 139,534,208-139,534,208 , GRCh37.p13 chr3: 123,277,863-123,277,863 , GRCh37.p13 chr7: 139,218,954-139,218,954 CLEC2L, HACD2, 1 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5319781copy number variation1nstd204human GRCh38.p13 chr7: 139,538,244-139,541,967 , GRCh37.p13 chr7: 139,222,990-139,226,713 CLEC2L
    nsv5255114copy number variation1nstd204human GRCh38.p13 chr7: 139,538,170-139,541,912 , GRCh37.p13 chr7: 139,222,916-139,226,658 CLEC2L
    nsv5243059copy number variation1nstd204human GRCh38.p13 chr7: 139,538,101-139,541,900 , GRCh37.p13 chr7: 139,222,847-139,226,646 CLEC2L
    nsv5243020copy number variation1nstd204human GRCh38.p13 chr7: 139,538,472-139,541,937 , GRCh37.p13 chr7: 139,223,218-139,226,683 CLEC2L
    nsv5202231mobile element deletion1nstd204human GRCh38.p13 chr7: 139,522,415-139,522,716 , GRCh37.p13 chr7: 139,207,161-139,207,462 CLEC2L
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968842copy number variation1nstd200human GRCh38 chr7: 139,536,649-139,538,271 , GRCh37.p13 chr7: 139,221,395-139,223,017 CLEC2L
    nsv4968841copy number variation1nstd200human GRCh38 chr7: 139,497,646-139,531,832 , GRCh37.p13 chr7: 139,182,392-139,216,578 CLEC2L, ST13P17
    nsv4968840copy number variation1nstd200human GRCh38 chr7: 139,480,513-139,546,714 , GRCh37.p13 chr7: 139,165,259-139,231,460 ERHP1, CLEC2L, 2 more genes
    nsv4958661copy number variation1nstd200human GRCh38 chr7: 139,520,744-139,522,673 , GRCh37.p13 chr7: 139,205,490-139,207,419 CLEC2L
    nsv4893237mobile element deletion1nstd200human GRCh38 chr7: 139,522,415-139,522,716 , GRCh37.p13 chr7: 139,207,161-139,207,462 CLEC2L
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