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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971324inversion1nstd209human GRCh38 chr9: 92,092,935-92,095,097 , GRCh37.p13 chr9: 94,855,217-94,857,379 SPTLC1
    nsv5925837copy number variation1nstd209human GRCh38 chr9: 92,102,644-92,102,952 , GRCh37.p13 chr9: 94,864,926-94,865,234 LOC100420896, SPTLC1
    nsv5923080copy number variation1nstd209human GRCh38 chr9: 92,058,220-92,058,295 , GRCh37.p13 chr9: 94,820,502-94,820,577 SPTLC1
    nsv5721755mobile element insertion1nstd211human GRCh38 chr9: 92,031,146-92,031,146 , GRCh37.p13 chr9: 94,793,428-94,793,428 SPTLC1
    nsv5719671mobile element insertion1nstd211human GRCh38 chr9: 92,081,212-92,081,212 , GRCh37.p13 chr9: 94,843,494-94,843,494 SPTLC1
    nsv5564511copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr9: 91,618,854-92,089,106 , GRCh37 chr9: 94,381,136-94,851,388 ROR2, SPTLC1, 6 more genes
    nsv5492569copy number variation1nstd206human GRCh38 chr9: 92,059,120-92,059,173 , GRCh37.p13 chr9: 94,821,402-94,821,455 SPTLC1
    nsv5484051copy number variation1nstd206human GRCh38 chr9: 92,058,223-92,058,296 , GRCh37.p13 chr9: 94,820,505-94,820,578 SPTLC1
    nsv5372798translocation1nstd200human GRCh38 chr9: 92,058,223-92,058,223 , GRCh38 chr9: 92,058,296-92,058,296 , GRCh37.p13 chr9: 94,820,505-94,820,505 , GRCh37.p13 chr9: 94,820,578-94,820,578 SPTLC1
    nsv5308206copy number variation1nstd204human GRCh38.p13 chr9: 91,466,831-92,159,147 , GRCh37.p13 chr9: 94,229,113-94,921,429 , HSPE1P22, 17 more genes
    nsv5258018copy number variation1nstd204human GRCh38.p13 chr9: 91,466,801-92,159,200 , GRCh37.p13 chr9: 94,229,083-94,921,482 , MTND4P15, 17 more genes
    nsv5244715copy number variation1nstd204human GRCh38.p13 chr9: 92,066,792-92,101,382 , GRCh37.p13 chr9: 94,829,074-94,863,664 SPTLC1
    nsv5126870mobile element insertion1nstd203human GRCh38 chr9: 92,106,237-92,106,249 , GRCh37.p13 chr9: 94,868,519-94,868,531 SPTLC1
    nsv4974702copy number variation1nstd200human GRCh38 chr9: 92,036,105-92,135,718 , GRCh37.p13 chr9: 94,798,387-94,898,000 LOC100128076, MTCO3P29, 5 more genes
    nsv4974699copy number variation1nstd200human GRCh38 chr9: 91,924,473-92,376,273 , GRCh37.p13 chr9: 94,686,755-95,138,555 , RPL21P82, 21 more genes
    nsv4974697copy number variation1nstd200human GRCh38 chr9: 91,466,839-92,159,143 , GRCh37.p13 chr9: 94,229,121-94,921,425 , MTCO3P29, 17 more genes
    nsv4973172copy number variation1nstd200human GRCh38 chr9: 92,098,886-92,102,126 , GRCh37.p13 chr9: 94,861,168-94,864,408 SPTLC1, LOC100420896
    nsv4973171copy number variation1nstd200human GRCh38 chr9: 92,087,371-92,099,510 , GRCh37.p13 chr9: 94,849,653-94,861,792 SPTLC1
    nsv4973170copy number variation1nstd200human GRCh38 chr9: 92,071,161-92,077,616 , GRCh37.p13 chr9: 94,833,443-94,839,898 SPTLC1
    nsv4973169copy number variation1nstd200human GRCh38 chr9: 92,064,209-92,064,868 , GRCh37.p13 chr9: 94,826,491-94,827,150 SPTLC1
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