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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098103copy number variation1nstd102humanPathogenic GRCh37 chr9: 98,690,981-98,691,166 , GRCh38.p12 chr9: 95,928,699-95,928,884 ERCC6L2
    nsv7077729inversion1nstd229human GRCh38 chr9: 94,417,509-96,970,614 , GRCh37.p13 chr9: 97,179,791-99,732,896 HSD17B3-AS1, ERCC6L2, 60 more genes
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7062513inversion1nstd229human GRCh38 chr9: 95,985,501-95,985,548 , GRCh37.p13 chr9: 98,747,783-98,747,830 ERCC6L2
    nsv7061823inversion1nstd229human GRCh38 chr9: 94,710,575-96,645,135 , GRCh37.p13 chr9: 97,472,857-99,407,417 LOC105376163, LINC00092, 42 more genes
    nsv6877371copy number variation1nstd229human GRCh38 chr9: 95,918,401-95,921,100 , GRCh37.p13 chr9: 98,680,683-98,683,382 PARK7P2, ERCC6L2
    nsv6876694copy number variation1nstd229human GRCh38 chr9: 96,027,637-96,103,276 , GRCh37.p13 chr9: 98,789,919-98,865,558 LOC158435, ERCC6L2, 1 more genes
    nsv6876139copy number variation1nstd229human GRCh38 chr9: 95,806,052-95,893,028 , GRCh37.p13 chr9: 98,568,334-98,655,310 ERCC6L2-AS1, RNU2-46P, 2 more genes
    nsv6875818copy number variation1nstd229human GRCh38 chr9: 95,688,189-96,229,236 , GRCh37.p13 chr9: 98,450,471-98,991,518 LOC107987103, LINC00092, 12 more genes
    nsv6875438copy number variation1nstd229human GRCh38 chr9: 96,026,921-96,026,967 , GRCh37.p13 chr9: 98,789,203-98,789,249 ERCC6L2, LOC105376159
    nsv6875059copy number variation1nstd229human GRCh38 chr9: 96,005,672-96,008,385 , GRCh37.p13 chr9: 98,767,954-98,770,667 ERCC6L2
    nsv6874399copy number variation1nstd229human GRCh38 chr9: 95,881,829-95,882,031 , GRCh37.p13 chr9: 98,644,111-98,644,313 ERCC6L2
    nsv6873098copy number variation1nstd229human GRCh38 chr9: 95,951,998-95,972,040 , GRCh37.p13 chr9: 98,714,280-98,734,322 ERCC6L2
    nsv6871461copy number variation1nstd229human GRCh38 chr9: 96,041,078-96,048,999 , GRCh37.p13 chr9: 98,803,360-98,811,281 ERCC6L2
    nsv6870821copy number variation1nstd229human GRCh38 chr9: 95,955,301-95,955,731 , GRCh37.p13 chr9: 98,717,583-98,718,013 ERCC6L2
    nsv6866483copy number variation1nstd229human GRCh38 chr9: 95,928,601-95,938,700 , GRCh37.p13 chr9: 98,690,883-98,700,982 ERCC6L2
    nsv6865151copy number variation1nstd229human GRCh38 chr9: 96,013,501-96,023,000 , GRCh37.p13 chr9: 98,775,783-98,785,282 LINC00092, LOC105376159, 1 more genes
    nsv6863314copy number variation1nstd229human GRCh38 chr9: 95,915,506-95,922,703 , GRCh37.p13 chr9: 98,677,788-98,684,985 ERCC6L2, PARK7P2
    nsv6863094copy number variation1nstd229human GRCh38 chr9: 95,882,726-95,894,650 , GRCh37.p13 chr9: 98,645,008-98,656,932 ERCC6L2
    nsv6862136copy number variation1nstd229human GRCh38 chr9: 95,896,910-95,901,889 , GRCh37.p13 chr9: 98,659,192-98,664,171 ERCC6L2
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