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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950997insertion1nstd209human GRCh38 chr9: 79,667,940-79,667,940 , GRCh37.p13 chr9: 82,282,855-82,282,855 TLE4
    nsv5921391copy number variation1nstd209human GRCh38 chr9: 79,590,410-79,590,460 , GRCh37.p13 chr9: 82,205,325-82,205,375 TLE4
    nsv5725612mobile element insertion1nstd211human GRCh38 chr9: 79,681,342-79,681,342 , GRCh37.p13 chr9: 82,296,257-82,296,257 TLE4
    nsv5719439mobile element insertion1nstd211human GRCh38 chr9: 79,667,846-79,667,846 , GRCh37.p13 chr9: 82,282,761-82,282,761 TLE4
    nsv5699995mobile element insertion1nstd211human GRCh38 chr9: 79,577,988-79,577,988 , GRCh37.p13 chr9: 82,192,903-82,192,903 TLE4
    nsv5695192mobile element insertion2nstd211human GRCh38 chr9: 79,681,342-79,681,342 , GRCh37.p13 chr9: 82,296,257-82,296,257 TLE4
    nsv5557962mobile element insertion1nstd206human GRCh38 chr9: 79,667,846-79,667,897 , GRCh37.p13 chr9: 82,282,761-82,282,812 TLE4
    nsv5487619copy number variation1nstd206human GRCh38 chr9: 79,712,325-79,712,431 , GRCh37.p13 chr9: 82,327,240-82,327,346 TLE4
    nsv5395060mobile element insertion1nstd206human GRCh38 chr9: 79,681,342-79,681,393 , GRCh37.p13 chr9: 82,296,257-82,296,308 TLE4
    nsv5372677translocation1nstd200human GRCh38 chr9: 79,713,606-79,713,606 , GRCh38 chr9: 79,714,499-79,714,499 , GRCh37.p13 chr9: 82,328,521-82,328,521 , GRCh37.p13 chr9: 82,329,414-82,329,414 TLE4
    nsv5197513mobile element insertion1nstd203human GRCh38 chr9: 79,606,187-79,606,187 , GRCh37.p13 chr9: 82,221,102-82,221,102 TLE4
    nsv5196054mobile element insertion1nstd203human GRCh38 chr9: 79,606,184-79,606,225 , GRCh37.p13 chr9: 82,221,099-82,221,140 TLE4
    nsv5192220mobile element insertion1nstd203human GRCh38 chr9: 79,667,831-79,667,843 , GRCh37.p13 chr9: 82,282,746-82,282,758 TLE4
    nsv5127382mobile element insertion1nstd203human GRCh38 chr9: 79,681,332-79,681,342 , GRCh37.p13 chr9: 82,296,247-82,296,257 TLE4
    nsv5122965mobile element insertion1nstd203human GRCh38 chr9: 79,681,326-79,681,348 , GRCh37.p13 chr9: 82,296,241-82,296,263 TLE4
    nsv5122657mobile element insertion1nstd203human GRCh38 chr9: 79,606,187-79,606,225 , GRCh37.p13 chr9: 82,221,102-82,221,140 TLE4
    nsv5036269inversion1nstd200human GRCh38 chr9: 79,108,237-87,224,469 , GRCh37.p13 chr9: 81,723,153-89,839,384 , RMI1, 100 more genes
    nsv4954873copy number variation1nstd200human GRCh38 chr9: 79,632,719-79,901,623 , GRCh37.p13 chr9: 82,247,634-82,516,538 NPAP1P6, LINC01507, 4 more genes
    nsv4952930copy number variation1nstd200human GRCh38 chr9: 79,670,694-79,674,347 , GRCh37.p13 chr9: 82,285,609-82,289,262 TLE4
    nsv4952929copy number variation1nstd200human GRCh38 chr9: 79,661,783-79,662,554 , GRCh37.p13 chr9: 82,276,698-82,277,469 TLE4
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