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nsv6313619

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:12,537,799
  • Description:GRCh37/hg19 2p23.2-21(chr2:29899368-42441440) AND not specified

Genome View

Select assembly:
Overlapping variant regions from other studies: 35906 SVs from 132 studies. See in: genome view    
Remapped(Score: Good):29,676,502-42,214,300Question Mark
Overlapping variant regions from other studies: 35933 SVs from 132 studies. See in: genome view    
Submitted genomic29,899,368-42,441,440Question Mark
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