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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961764insertion1nstd209human GRCh38 chr9: 81,749,598-81,749,598 , GRCh37.p13 chr9: 84,364,513-84,364,513 TLE1-DT
    nsv5921227copy number variation1nstd209human GRCh38 chr9: 81,713,728-81,714,030 , GRCh37.p13 chr9: 84,328,643-84,328,945 TLE1-DT
    nsv5584690copy number variation1nstd207human GRCh38 chr9: 81,709,433-81,712,010 , GRCh37.p13 chr9: 84,324,348-84,326,925 TLE1-DT
    nsv5483719copy number variation1nstd206human GRCh38 chr9: 81,755,304-81,755,398 , GRCh37.p13 chr9: 84,370,219-84,370,313 TLE1-DT
    nsv5479790copy number variation1nstd206human GRCh38 chr9: 81,709,428-81,712,031 , GRCh37.p13 chr9: 84,324,343-84,326,946 TLE1-DT
    nsv5393799mobile element deletion1nstd186human GRCh37 chr9: 84,324,363-84,326,926 , GRCh38.p12 chr9: 81,709,448-81,712,011 TLE1-DT
    nsv5372693translocation1nstd200human GRCh38 chr9: 81,763,064-81,763,064 , GRCh38 chr9: 81,763,310-81,763,310 , GRCh37.p13 chr9: 84,377,979-84,377,979 , GRCh37.p13 chr9: 84,378,225-84,378,225 TLE1-DT
    nsv5345385translocation1nstd200human GRCh37 chr9: 84,324,369-84,324,369 , GRCh37 chr9: 84,327,001-84,327,001 , GRCh38.p12 chr9: 81,712,086-81,712,086 , GRCh38.p12 chr9: 81,709,454-81,709,454 TLE1-DT
    nsv5325140mobile element deletion1nstd204human GRCh38.p13 chr9: 81,709,448-81,712,011 , GRCh37.p13 chr9: 84,324,363-84,326,926 TLE1-DT
    nsv5139721mobile element insertion1nstd203human GRCh38 chr9: 81,774,502-81,774,517 , GRCh37.p13 chr9: 84,389,417-84,389,432 TLE1-DT
    nsv5128376mobile element insertion1nstd203human GRCh38 chr9: 81,750,899-81,750,926 , GRCh37.p13 chr9: 84,365,814-84,365,841 TLE1-DT
    nsv5036269inversion1nstd200human GRCh38 chr9: 79,108,237-87,224,469 , GRCh37.p13 chr9: 81,723,153-89,839,384 , RMI1, 100 more genes
    nsv5034970mobile element deletion1nstd200human GRCh38 chr9: 81,709,448-81,712,011 , GRCh37.p13 chr9: 84,324,363-84,326,926 TLE1-DT
    nsv4952993copy number variation1nstd200human GRCh38 chr9: 81,706,171-81,706,351 , GRCh37.p13 chr9: 84,321,086-84,321,266 TLE1-DT
    nsv4814229copy number variation1nstd200human GRCh37 chr9: 84,377,979-84,378,225 , GRCh38.p12 chr9: 81,763,064-81,763,310 TLE1-DT
    nsv4739405copy number variation1nstd199human GRCh37 chr9: 84,324,355-84,326,934 , GRCh38.p12 chr9: 81,709,440-81,712,019 TLE1-DT
    nsv4712835copy number variation4nstd195human GRCh37 chr9: 84,324,348-84,324,349 , GRCh38.p12 chr9: 81,709,433-81,709,434 TLE1-DT
    nsv4657526copy number variation1nstd186human GRCh37 chr9: 84,324,363-84,326,942 , GRCh38.p12 chr9: 81,709,448-81,712,027 TLE1-DT
    nsv4526373copy number variation1nstd166human GRCh37.p13 chr9: 84,325,268-84,325,351 , GRCh38.p12 chr9: 81,710,353-81,710,436 TLE1-DT
    nsv4526262copy number variation1nstd166human GRCh37.p13 chr9: 84,338,223-84,338,282 , GRCh38.p12 chr9: 81,723,308-81,723,367 RNU6-1035P, TLE1-DT
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