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Items: 1 to 20 of 372

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973283inversion1nstd209human GRCh38 chr17: 76,181,651-76,183,209 , GRCh37.p13 chr17: 74,177,732-74,179,290 RNF157
    nsv5938111copy number variation1nstd209human GRCh38 chr17: 76,221,080-76,225,130 , GRCh37.p13 chr17: 74,217,161-74,221,211 RNF157, ATF4P3
    nsv5937144copy number variation1nstd209human GRCh38 chr17: 76,170,145-76,171,676 , GRCh37.p13 chr17: 74,166,226-74,167,757 RNF157
    nsv5931997copy number variation1nstd209human GRCh38 chr17: 76,214,940-76,223,796 , GRCh37.p13 chr17: 74,211,021-74,219,877 RNF157, ATF4P3
    nsv5883858copy number variation1nstd209human GRCh38 chr17: 76,220,020-76,223,769 , GRCh37.p13 chr17: 74,216,101-74,219,850 ATF4P3, RNF157
    nsv5879162copy number variation1nstd209human GRCh38 chr17: 76,170,122-76,171,621 , GRCh37.p13 chr17: 74,166,203-74,167,702 RNF157
    nsv5874392copy number variation1nstd209human GRCh38 chr17: 76,215,620-76,223,819 , GRCh37.p13 chr17: 74,211,701-74,219,900 RNF157, ATF4P3
    nsv5730400mobile element insertion1nstd211human GRCh38 chr17: 76,165,248-76,165,248 , GRCh37.p13 chr17: 74,161,329-74,161,329 RNF157
    nsv5723638mobile element insertion1nstd211human GRCh38 chr17: 76,221,680-76,221,680 , GRCh37.p13 chr17: 74,217,761-74,217,761 RNF157
    nsv5667382inversion1nstd207human GRCh37.p13 chr17: 74,177,732-74,179,282 , GRCh38 chr17: 76,181,651-76,183,201 RNF157
    nsv5591358copy number variation1nstd207human GRCh38 chr17: 76,182,914-76,183,184 , GRCh37.p13 chr17: 74,178,995-74,179,265 RNF157
    nsv5554359inversion1nstd206human GRCh38 chr17: 76,181,856-76,183,230 , GRCh37.p13 chr17: 74,177,937-74,179,311 RNF157
    nsv5533846copy number variation1nstd206human GRCh38 chr17: 76,170,147-76,171,677 , GRCh37.p13 chr17: 74,166,228-74,167,758 RNF157
    nsv5528357copy number variation1nstd206human GRCh38 chr17: 76,231,366-76,233,266 , GRCh37.p13 chr17: 74,227,447-74,229,347 RNF157
    nsv5525176copy number variation1nstd206human GRCh38 chr17: 76,171,146-76,171,442 , GRCh37.p13 chr17: 74,167,227-74,167,523 RNF157
    nsv5524416copy number variation1nstd206human GRCh38 chr17: 76,177,009-76,179,983 , GRCh37.p13 chr17: 74,173,090-74,176,064 RNF157
    nsv5520417copy number variation1nstd206human GRCh38 chr17: 76,234,352-76,235,106 , GRCh37.p13 chr17: 74,230,433-74,231,187 RNF157
    nsv5519926copy number variation1nstd206human GRCh38 chr17: 76,176,756-76,177,647 , GRCh37.p13 chr17: 74,172,837-74,173,728 RNF157
    nsv5519541copy number variation1nstd206human GRCh38 chr17: 76,182,762-76,182,871 , GRCh37.p13 chr17: 74,178,843-74,178,952 RNF157
    nsv5517459copy number variation1nstd206human GRCh38 chr17: 76,228,483-76,228,564 , GRCh37.p13 chr17: 74,224,564-74,224,645 RNF157
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