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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6115368copy number variation1nstd186human GRCh37 chr9: 68,397,473-68,413,191 , GRCh38.p12 chr9: 63,801,739-63,817,457 LINC00537, RNA5SP284, 1 more genes
    nsv5924488copy number variation1nstd209human GRCh38 chr9: 63,813,586-63,814,512 , GRCh37.p13 chr9: 68,409,320-68,410,246 LINC00537, RNA5SP284
    nsv5919501copy number variation1nstd209human GRCh38 chr9: 61,557,000-65,487,786 , GRCh37.p13 chr: NaN-NaN , MTCO1P36, 98 more genes
    nsv5918216copy number variation1nstd209human GRCh38 chr9: 61,647,960-65,578,967 , GRCh37.p13 chr: NaN-NaN , SDR42E1P3, 99 more genes
    nsv5914589copy number variation1nstd209human GRCh38 chr9: 63,812,014-63,812,091 , GRCh37.p13 chr9: 68,407,748-68,407,825 LINC00537, RNA5SP284
    nsv5914346copy number variation1nstd209human GRCh38 chr9: 60,768,680-66,674,368 , GRCh37.p13 chr: NaN-NaN , MEP1AP3, 146 more genes
    nsv5912313copy number variation1nstd209human GRCh38 chr9: 63,816,051-63,816,173 , GRCh37.p13 chr9: 68,411,785-68,411,907 DUX4L50, LINC00537
    nsv5910323copy number variation1nstd209human GRCh38 chr9: 61,604,972-65,538,433 , GRCh37.p13 chr: NaN-NaN , FAM242E, 98 more genes
    nsv5704427mobile element insertion2nstd211human GRCh38 chr9: 63,819,238-63,819,238 , GRCh37.p13 chr9: 68,414,972-68,414,972 MIR4477B, LINC00537
    nsv5592805copy number variation1nstd207human GRCh38 chr9: 63,812,014-63,812,091 , GRCh37.p13 chr9: 68,407,748-68,407,825 LINC00537, RNA5SP284
    nsv5487999copy number variation1nstd206human GRCh38 chr9: 63,816,053-63,816,174 , GRCh37.p13 chr9: 68,411,787-68,411,908 DUX4L50, LINC00537
    nsv5481028copy number variation1nstd206human GRCh38 chr9: 63,813,589-63,814,513 , GRCh37.p13 chr9: 68,409,323-68,410,247 LINC00537, RNA5SP284
    nsv5372532translocation1nstd200human GRCh38 chr9: 63,816,496-63,816,496 , GRCh38 chr9: 62,798,935-62,798,935 , GRCh37.p13 chr9: 68,412,230-68,412,230 , GRCh37.p13 chr9: 66,454,759-66,454,759 LINC00537, DUX4L50
    nsv5258329copy number variation1nstd204human GRCh38.p13 chr9: 63,809,578-63,815,242 , GRCh37.p13 chr9: 68,405,312-68,410,976 RNA5SP284, LINC00537
    nsv5255406copy number variation1nstd204human GRCh38.p13 chr9: 63,815,732-63,818,276 , GRCh37.p13 chr9: 68,411,466-68,414,010 MIR4477B, DUX4L50, 1 more genes
    nsv5255017copy number variation1nstd204human GRCh38.p13 chr9: 63,809,403-63,813,335 , GRCh37.p13 chr9: 68,405,137-68,409,069 RNA5SP284, LINC00537
    nsv5254990copy number variation1nstd204human GRCh38.p13 chr9: 63,818,177-63,820,483 , GRCh37.p13 chr9: 68,413,911-68,416,217 MIR4477B, DUX4L50, 1 more genes
    nsv5254886copy number variation1nstd204human GRCh38.p13 chr9: 63,811,337-63,817,225 , GRCh37.p13 chr9: 68,407,071-68,412,959 DUX4L50, LINC00537, 1 more genes
    nsv5253528copy number variation1nstd204human GRCh38.p13 chr9: 63,814,458-63,816,775 , GRCh37.p13 chr9: 68,410,192-68,412,509 DUX4L50, LINC00537
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