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Items: 1 to 20 of 440

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128441insertion1nstd186human GRCh37 chr4: 56,371,945-56,371,945 , GRCh38.p12 chr4: 55,505,778-55,505,778 CLOCK
    nsv5955973insertion1nstd209human GRCh38 chr4: 55,505,778-55,505,778 , GRCh37.p13 chr4: 56,371,945-56,371,945 CLOCK
    nsv5955589insertion1nstd209human GRCh38 chr4: 55,503,978-55,503,978 , GRCh37.p13 chr4: 56,370,145-56,370,145 CLOCK
    nsv5902972copy number variation1nstd209human GRCh38 chr4: 55,487,270-55,490,367 , GRCh37.p13 chr4: 56,353,437-56,356,534 CLOCK
    nsv5900416copy number variation1nstd209human GRCh38 chr4: 55,445,105-55,445,255 , GRCh37.p13 chr4: 56,311,272-56,311,422 TMEM165, CLOCK
    nsv5889939copy number variation1nstd209human GRCh38 chr4: 55,501,366-55,501,429 , GRCh37.p13 chr4: 56,367,533-56,367,596 CLOCK
    nsv5839965copy number variation1nstd209human GRCh38 chr4: 55,487,464-55,490,357 , GRCh37.p13 chr4: 56,353,631-56,356,524 CLOCK
    nsv5727571mobile element insertion1nstd211human GRCh38 chr4: 55,483,283-55,483,283 , GRCh37.p13 chr4: 56,349,450-56,349,450 CLOCK
    nsv5693057mobile element insertion1nstd211human GRCh38 chr4: 55,439,965-55,439,965 , GRCh37.p13 chr4: 56,306,132-56,306,132 TMEM165, CLOCK
    nsv5687494mobile element insertion2nstd211human GRCh38 chr4: 55,505,795-55,505,795 , GRCh37.p13 chr4: 56,371,962-56,371,962 CLOCK
    nsv5675471mobile element insertion2nstd211human GRCh38 chr4: 55,468,614-55,468,614 , GRCh37.p13 chr4: 56,334,781-56,334,781 CLOCK
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5612988insertion1nstd207human GRCh38 chr4: 55,505,778-55,505,778 , GRCh37.p13 chr4: 56,371,945-56,371,945 CLOCK
    nsv5578943copy number variation1nstd207human GRCh38 chr4: 55,445,104-55,445,256 , GRCh37.p13 chr4: 56,311,271-56,311,423 CLOCK, TMEM165
    nsv5542497insertion1nstd206human GRCh38 chr4: 55,505,778-55,505,778 , GRCh37.p13 chr4: 56,371,945-56,371,945 CLOCK
    nsv5471987copy number variation1nstd206human GRCh38 chr4: 55,445,445-55,445,540 , GRCh37.p13 chr4: 56,311,612-56,311,707 CLOCK, TMEM165
    nsv5465885copy number variation1nstd206human GRCh38 chr4: 55,482,161-55,482,293 , GRCh37.p13 chr4: 56,348,328-56,348,460 CLOCK
    nsv5465804copy number variation1nstd206human GRCh38 chr4: 55,445,105-55,445,276 , GRCh37.p13 chr4: 56,311,272-56,311,443 TMEM165, CLOCK
    nsv5458099copy number variation1nstd206human GRCh38 chr4: 55,531,545-55,533,223 , GRCh37.p13 chr4: 56,397,712-56,399,390 CLOCK
    nsv5412014mobile element insertion1nstd206human GRCh38 chr4: 55,468,614-55,468,665 , GRCh37.p13 chr4: 56,334,781-56,334,832 CLOCK
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