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nsv3923415

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:3,733,737
  • Description:GRCh38/hg38 19p13.2-13.12(chr19:10315258-14048994)x3 AND See cases

Genome View

Select assembly:
Overlapping variant regions from other studies: 12682 SVs from 114 studies. See in: genome view    
Submitted genomic10,315,258-14,048,994Question Mark
Overlapping variant regions from other studies: 12686 SVs from 114 studies. See in: genome view    
Submitted genomic10,425,934-14,159,806Question Mark
Overlapping variant regions from other studies: 2339 SVs from 35 studies. See in: genome view    
Submitted genomic10,286,934-14,020,806Question Mark
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