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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5917205copy number variation1nstd209human GRCh38 chr9: 128,079,682-128,080,053 , GRCh37.p13 chr9: 130,841,961-130,842,332 SLC25A25
    nsv5912630copy number variation1nstd209human GRCh38 chr9: 128,087,847-128,087,960 , GRCh37.p13 chr9: 130,850,126-130,850,239 SLC25A25
    nsv5713888mobile element insertion1nstd211human GRCh38 chr9: 128,109,224-128,109,224 , GRCh37.p13 chr9: 130,871,503-130,871,503 SLC25A25, SLC25A25-AS1
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 PIP5KL1, MIR3911, 50 more genes
    nsv5402820mobile element insertion1nstd206human GRCh38 chr9: 128,109,224-128,109,252 , GRCh37.p13 chr9: 130,871,503-130,871,531 SLC25A25, SLC25A25-AS1
    nsv5255143copy number variation1nstd204human GRCh38.p13 chr9: 128,000,401-128,091,700 , GRCh37.p13 chr9: 130,762,680-130,853,979 SLC25A25, NAIF1
    nsv5254554copy number variation1nstd204human GRCh37.p13 chr9: 130,644,780-130,830,179 , GRCh38.p13 chr9: 127,882,501-128,067,900 AK1, DPM2, 6 more genes
    nsv5243983copy number variation1nstd204human GRCh38.p13 chr9: 127,720,701-128,119,000 , GRCh37.p13 chr9: 130,482,980-130,881,279 MIR2861, ENG, 21 more genes
    nsv5243279copy number variation1nstd204human GRCh38.p13 chr9: 128,078,601-128,081,300 , GRCh37.p13 chr9: 130,840,880-130,843,579 SLC25A25
    nsv5128274mobile element insertion1nstd203human GRCh38 chr9: 128,083,676-128,083,691 , GRCh37.p13 chr9: 130,845,955-130,845,970 SLC25A25
    nsv5125207mobile element insertion1nstd203human GRCh38 chr9: 128,109,210-128,109,224 , GRCh37.p13 chr9: 130,871,489-130,871,503 SLC25A25-AS1, SLC25A25
    nsv5123644mobile element insertion1nstd203human GRCh38 chr9: 128,069,895-128,069,949 , GRCh37.p13 chr9: 130,832,174-130,832,228 SLC25A25
    nsv4988374copy number variation1nstd200human GRCh38 chr9: 128,083,798-128,086,576 , GRCh37.p13 chr9: 130,846,077-130,848,855 SLC25A25
    nsv4988373copy number variation1nstd200human GRCh38 chr9: 128,079,740-128,081,669 , GRCh37.p13 chr9: 130,842,019-130,843,948 SLC25A25
    nsv4985740copy number variation1nstd200human GRCh38 chr9: 128,105,845-128,709,294 , GRCh37.p13 chr9: 130,868,124-131,471,573 , SET, 33 more genes
    nsv4985739copy number variation1nstd200human GRCh38 chr9: 128,071,963-128,079,786 , GRCh37.p13 chr9: 130,834,242-130,842,065 SLC25A25
    nsv4985738copy number variation1nstd200human GRCh38 chr9: 128,030,482-128,145,703 , GRCh37.p13 chr9: 130,792,761-130,907,982 SLC25A25-AS1, NAIF1, 3 more genes
    nsv4985735copy number variation1nstd200human GRCh38 chr9: 127,951,402-128,083,324 , GRCh37.p13 chr9: 130,713,681-130,845,603 NAIF1, SLC25A25, 1 more genes
    nsv4983734copy number variation1nstd200human GRCh38 chr9: 128,108,655-128,111,481 , GRCh37.p13 chr9: 130,870,934-130,873,760 SLC25A25-AS1, SLC25A25
    nsv4844716copy number variation1nstd200human GRCh37 chr9: 130,842,043-130,843,943 , GRCh38.p12 chr9: 128,079,764-128,081,664 SLC25A25
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