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nsv6636352

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:231,151
  • Description:GRCh37/hg19 2p22.1(chr2:39040762-39271911)x1 AND not provided

Genome View

Select assembly:
Overlapping variant regions from other studies: 704 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):38,813,620-39,044,770Question Mark
Overlapping variant regions from other studies: 704 SVs from 71 studies. See in: genome view    
Submitted genomic39,040,762-39,271,911Question Mark
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