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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5909034copy number variation1nstd209human GRCh38 chr10: 97,440,959-97,483,202 , GRCh37.p13 chr10: 99,200,716-99,242,959 EXOSC1, MMS19, 1 more genes
    nsv5851103copy number variation1nstd209human GRCh38 chr10: 97,441,026-97,459,470 , GRCh37.p13 chr10: 99,200,783-99,219,227 EXOSC1, MMS19, 1 more genes
    nsv5695342mobile element insertion2nstd211human GRCh38 chr10: 97,457,442-97,457,442 , GRCh37.p13 chr10: 99,217,199-99,217,199 MMS19, ZDHHC16
    nsv5641986insertion1nstd207human GRCh38 chr10: 97,457,425-97,457,425 , GRCh37.p13 chr10: 99,217,182-99,217,182 ZDHHC16, MMS19
    nsv5477723copy number variation1nstd206human GRCh38 chr10: 97,428,986-97,444,278 , GRCh37.p13 chr10: 99,188,743-99,204,035 ZDHHC16, PGAM1, 1 more genes
    nsv5406340mobile element insertion1nstd206human GRCh38 chr10: 97,450,788-97,450,839 , GRCh37.p13 chr10: 99,210,545-99,210,596 ZDHHC16
    nsv5331254translocation1nstd200human GRCh37 chr10: 99,214,651-99,214,651 , GRCh37 chr10: 99,214,573-99,214,573 , GRCh38.p12 chr10: 97,454,816-97,454,816 , GRCh38.p12 chr10: 97,454,894-97,454,894 ZDHHC16
    nsv5314709copy number variation1nstd204human GRCh37.p13 chr10: 99,177,371-99,269,971 , GRCh38.p13 chr10: 97,417,614-97,510,214 PGAM1, EXOSC1, 4 more genes
    nsv5259980copy number variation1nstd204human GRCh38.p13 chr10: 97,439,226-97,446,524 , GRCh37.p13 chr10: 99,198,983-99,206,281 ZDHHC16, EXOSC1
    nsv5254809copy number variation1nstd204human GRCh37.p13 chr10: 99,177,558-99,269,657 , GRCh38.p13 chr10: 97,417,801-97,509,900 PGAM1, EXOSC1, 4 more genes
    nsv5252284copy number variation1nstd204human GRCh38.p13 chr10: 97,420,016-97,459,857 , GRCh37.p13 chr10: 99,179,773-99,219,614 EXOSC1, PGAM1, 3 more genes
    nsv5136713mobile element insertion1nstd203human GRCh38 chr10: 97,449,882-97,449,928 , GRCh37.p13 chr10: 99,209,639-99,209,685 ZDHHC16
    nsv5134401mobile element insertion1nstd203human GRCh38 chr10: 97,457,425-97,457,442 , GRCh37.p13 chr10: 99,217,182-99,217,199 MMS19, ZDHHC16
    nsv5120558mobile element insertion1nstd203human GRCh38 chr10: 97,457,432-97,457,442 , GRCh37.p13 chr10: 99,217,189-99,217,199 ZDHHC16, MMS19
    nsv4986862copy number variation1nstd200human GRCh38 chr10: 97,454,816-97,454,894 , GRCh37.p13 chr10: 99,214,573-99,214,651 ZDHHC16
    nsv4899577mobile element deletion1nstd200human GRCh38 chr10: 97,446,727-97,447,006 , GRCh37.p13 chr10: 99,206,484-99,206,763 ZDHHC16
    nsv4774809mobile element deletion1nstd200human GRCh37 chr10: 99,206,484-99,206,763 , GRCh38.p12 chr10: 97,446,727-97,447,006 ZDHHC16
    nsv4618034copy number variation1nstd183human GRCh37 chr10: 99,205,703-99,205,892 , GRCh38.p12 chr10: 97,445,946-97,446,135 EXOSC1, ZDHHC16
    nsv4481903mobile element insertion1nstd166human GRCh37.p13 chr10: 99,217,182-99,217,182 , GRCh38.p12 chr10: 97,457,425-97,457,425 MMS19, ZDHHC16
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