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VWF Sequence Analysis (All Exons)

Order Code: 1395

Also Known as

Von Willebrand Disease, VWF

Disease State

Test Information

Sequence analysis of the VWF gene (exons 1-52) detects germline variants associated with von Willebrand disease (VWD). VWF analysis is appropriate for all types of VWD.

Sample Requirements

Amniotic Fluid, Buccal Swabs, Cultured Amniocytes, CVS, DNA, EDTA Bone Marrow, EDTA Whole Blood

Shipping Information

Room Temperature

Requested Volume

3-5 mL EDTA Whole Blood or Bone Marrow (lavender top), 3-4 Buccal Swabs, 1 ug DNA at 50 ng/uL, 7-15 mL Amniotic Fluid, 5-10 mg CVS, 2-T25 flasks cultured amniocytes or CVS (2x10^6 minimum)

Minimum/Pediatric Volume

Fetal: Call Laboratory; Parental/Patient: 2 ml

CPT Codes

81408

Method

Capture Hybridization and Next Generation Sequencing (MiSeq) with supplementary Sanger for quality and coverage or PCR and Bi-directional DNA Sequencing

Turnaround Time

21 days

New York State Approval

Approved

DEX Z-Code™

Yes, visit app.dexzcodes.com

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