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nsv3922263

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:3,598,246
  • Description:GRCh38/hg38 9q33.2-33.3(chr9:123095598-126693843)x1 AND See cases

Genome View

Select assembly:
Overlapping variant regions from other studies: 9078 SVs from 106 studies. See in: genome view    
Submitted genomic123,095,598-126,693,843Question Mark
Overlapping variant regions from other studies: 9078 SVs from 106 studies. See in: genome view    
Submitted genomic125,857,877-129,456,122Question Mark
Overlapping variant regions from other studies: 2226 SVs from 28 studies. See in: genome view    
Submitted genomic124,897,698-128,495,943Question Mark
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