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Items: 1 to 20 of 357

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950842insertion1nstd209human GRCh38 chr9: 81,675,707-81,675,707 , GRCh37.p13 chr9: 84,290,622-84,290,622 TLE1
    nsv5924081copy number variation1nstd209human GRCh38 chr9: 81,644,735-81,645,100 , GRCh37.p13 chr9: 84,259,650-84,260,015 TLE1
    nsv5914872copy number variation1nstd209human GRCh38 chr9: 81,612,979-81,613,064 , GRCh37.p13 chr9: 84,227,894-84,227,979 TLE1
    nsv5913582copy number variation1nstd209human GRCh38 chr9: 81,615,656-81,615,728 , GRCh37.p13 chr9: 84,230,571-84,230,643 TLE1
    nsv5908411copy number variation1nstd209human GRCh38 chr9: 81,575,515-81,587,330 , GRCh37.p13 chr9: 84,190,430-84,202,245 TLE1, LOC105376106
    nsv5907591copy number variation1nstd209human GRCh38 chr9: 81,645,529-81,647,194 , GRCh37.p13 chr9: 84,260,444-84,262,109 TLE1
    nsv5866111copy number variation1nstd209human GRCh38 chr9: 81,627,611-81,629,860 , GRCh37.p13 chr9: 84,242,526-84,244,775 TLE1
    nsv5860485copy number variation1nstd209human GRCh38 chr9: 81,594,569-81,597,268 , GRCh37.p13 chr9: 84,209,484-84,212,183 TLE1
    nsv5855360copy number variation1nstd209human GRCh38 chr9: 81,581,826-81,587,129 , GRCh37.p13 chr9: 84,196,741-84,202,044 LOC105376106, TLE1
    nsv5852492copy number variation1nstd209human GRCh38 chr9: 81,585,130-81,587,529 , GRCh37.p13 chr9: 84,200,045-84,202,444 LOC105376106, TLE1
    nsv5851974copy number variation1nstd209human GRCh38 chr9: 81,645,466-81,646,699 , GRCh37.p13 chr9: 84,260,381-84,261,614 TLE1
    nsv5701863mobile element insertion1nstd211human GRCh38 chr9: 81,657,562-81,657,562 , GRCh37.p13 chr9: 84,272,477-84,272,477 TLE1
    nsv5694418mobile element insertion1nstd211human GRCh38 chr9: 81,637,661-81,637,661 , GRCh37.p13 chr9: 84,252,576-84,252,576 TLE1
    nsv5590600copy number variation1nstd207human GRCh38 chr9: 81,615,656-81,615,728 , GRCh37.p13 chr9: 84,230,571-84,230,643 TLE1
    nsv5557958sequence alteration1nstd206human GRCh38 chr9: 81,661,629-81,663,105 , GRCh37.p13 chr9: 84,276,544-84,278,020 TLE1
    nsv5546986insertion1nstd206human GRCh38 chr9: 81,663,105-81,663,105 , GRCh37.p13 chr9: 84,278,020-84,278,020 TLE1
    nsv5546254insertion1nstd206human GRCh38 chr9: 81,681,575-81,681,615 , GRCh37.p13 chr9: 84,296,490-84,296,530 TLE1
    nsv5491247copy number variation1nstd206human GRCh38 chr9: 81,615,658-81,615,729 , GRCh37.p13 chr9: 84,230,573-84,230,644 TLE1
    nsv5490051copy number variation1nstd206human GRCh38 chr9: 81,644,715-81,645,121 , GRCh37.p13 chr9: 84,259,630-84,260,036 TLE1
    nsv5488066copy number variation1nstd206human GRCh38 chr9: 81,662,416-81,663,110 , GRCh37.p13 chr9: 84,277,331-84,278,025 TLE1
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