Search Tests - PreventionGenetics

Menu

  • Menu
  • Testing

      Test Menu

      • PGnome
      • PGxome
      • Custom Panels
      • Tests by Category
      • Targeted Variants
      • How To Order
      • Prenatal
      • All Tests
      • Tests by Disease

      Partner Programs

      • Sponsored Testing
      • Partnership Information
  • Billing

      Billing Information

      • Benefits Investigation
      • Billing Policy
      • CPT Codes
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • Resources

      Test Information

      • Sample Reports
      • Test Methods
      • Variant Interpretation
      • Family Testing

      Education

      • Disease Prevention
      • Webinars

      Policies

      • Terms & Conditions
      • Privacy Practices & Policies
  • How to Order

      Process

      • Log In / myPrevent
      • Ordering Instructions
      • Ordering Instructions
      • Report Retrieval
      • Turnaround Time
      • Forms
      • Order Kits

      Additional Info

      • Specimens & Shipping
      • Sample Reports
      • FAQs
      • Sending NY Specimens
      • Family Follow-up Testing
  • DNA Banking

      Providers

      • About DNA Banking
      • Order DNA Banking
      • Order Banking Kits
      • Paper Forms
      • Specimen Requirements
      • Post-Mortem DNA Banking
      • Resources
      • FAQs
      • PGDNABank
        For Patients
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Senior Staff
      • Quality & Value
      • Publications
      • Newsletters
      • Licenses and Certificates
      • PGNewsroom
      • Join Our Team
  • myPrevent
    • myPrevent Home
    • Variant Interpretation Service
    • Patient Orders & Reports
    • My Profile
    • Support
  • Contact Us
  • Forms
    • 0

    • Log In / Sign Up

      myPrevent

  • Menu
HOME | CONTACT US | FORMS |

Log In / Sign Up

myPrevent

|

0

  • Testing

      Test Menu

      • PGnome
      • PGxome
      • Custom Panels
      • Tests by Category
      • Targeted Variants
      • How To Order
      • Prenatal
      • All Tests
      • Tests by Disease

      Partner Programs

      • Sponsored Testing
      • Partnership Information
  • |
  • Billing

      Billing Information

      • Benefits Investigation
      • Billing Policy
      • CPT Codes
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • |
  • Resources

      Test Information

      • Sample Reports
      • Test Methods
      • Variant Interpretation
      • Family Testing

      Education

      • Disease Prevention
      • Webinars

      Policies

      • Terms & Conditions
      • Privacy Practices & Policies
  • |
  • How to Order

      Process

      • Log In / myPrevent
      • Ordering Instructions
      • Ordering Instructions
      • Report Retrieval
      • Turnaround Time
      • Forms
      • Order Kits

      Additional Info

      • Specimens & Shipping
      • Sample Reports
      • FAQs
      • Sending NY Specimens
      • Family Follow-up Testing
  • |
  • DNA Banking

      Providers

      • About DNA Banking
      • Order DNA Banking
      • Order Banking Kits
      • Paper Forms
      • Specimen Requirements
      • Post-Mortem DNA Banking
      • Resources
      • FAQs
      • PGDNABank
        For Patients
  • |
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Senior Staff
      • Quality & Value
      • Publications
      • Newsletters
      • Licenses and Certificates
      • PGNewsroom
      • Join Our Team

Browser Upgrade Recommended. More Info

We have detected that you are using Internet Explorer or Microsoft Edge Legacy. Please consider upgrading your browser to any of the following for the best experience.

  • Google Chrome
  • Firefox
  • Microsoft Edge
  • Safari

Login

Forgot username?

Forgot password?

Don't have an account?

×
  • GO BACK
    Test By Category
  • View All Tests
  • View All Panels
ORDER
Test Kits
START
Custom Panel

METHOD KEY

  • Sequencing with CNV
    PGxome
  • Sequencing with CNV
    PG-Select
  • CNV via aCGH
  • Sanger Sequencing
  • MLPA
  • Repeat Expansion
  • Other

Search Results

Test Descriptions Found: 53
Searched: all tests

# A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Panel(s) Available Method Price
Oculocutaneous Albinism (OCA) Panel
Sequencing with CNV
PGxome
$890
Omenn Syndrome Panel
Sequencing with CNV
PGxome
$890
Opitz G/BBB Syndrome Panel
Sequencing with CNV
PGxome
$1100
Optic Atrophy Panel
Sequencing with CNV
PGxome
$890
Organic Aciduria Panel
Sequencing with CNV
PGxome
$930
Osteogenesis Imperfecta and Hypophosphatasia (HPP) Panel
Sequencing with CNV
PGxome
$960
Osteogenesis Imperfecta Panel
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta, Hypophosphatasia (HPP), and Inherited Hypophosphatemic Rickets Panel
Sequencing with CNV
PGxome
$1140
Overgrowth and Macrocephaly Syndromes Panel
Sequencing with CNV
PGxome
$990
Single Gene Test(s) Available Method Price
Ocular Albinism (OA1) via the GPR143 Gene
Sanger Sequencing
$810
Sequencing with CNV
PGxome
$890
Oculocerebrorenal Syndrome of Lowe (Lowe syndrome) and Dent Disease - 2 via the OCRL Gene
Sanger Sequencing
$1280
Sequencing with CNV
PGxome
$890
Oculocutaneous Albinism in Griscelli syndrome via the MYO5A Gene
Sanger Sequencing
$2200
Sequencing with CNV
PGxome
$890
Oculocutaneous Albinism Type 1 (OCAI) via the TYR Gene
Sanger Sequencing
$680
Sequencing with CNV
PGxome
$890
Oculocutaneous Albinism Type 2 (OCAII) via the OCA2 Gene
Sanger Sequencing
$1310
Sequencing with CNV
PGxome
$890
Oculocutaneous Albinism Type 2 (OCAII) via the OCA2 Known Intragenic Gross Deletion
Other
$250
Oculocutaneous Albinism Type 3 (OCAIII) via the TYRP1 Gene
Sanger Sequencing
$750
Sequencing with CNV
PGxome
$890
Oculocutaneous Albinism Type 4 (OCAIV) via the SLC45A2 Gene
Sanger Sequencing
$780
Sequencing with CNV
PGxome
$890
Oculocutaneous Albinism Type 6 (OCAVI) via the SLC24A5 Gene
Sanger Sequencing
$750
Sequencing with CNV
PGxome
$890
Oculocutaneous Albinism Type 7 (OCAVII) via the LRMDA (C10orf11) Gene
Sanger Sequencing
$610
Sequencing with CNV
PGxome
$890
OculoDentoDigital Dysplasia (ODDD) via the GJA1 Gene
Sanger Sequencing
$250
Sequencing with CNV
PGxome
$890
Oculofaciocardiodental Syndrome and Lenz Microphthalmia Syndrome via the BCOR Gene
Sanger Sequencing
$1250
Sequencing with CNV
PGxome
$890
Oculopharyngeal Muscular Dystrophy via the PABPN1 (GCN) Repeat Expansion
Other
$390
Oguchi Disease and Retinitis Pigmentosa (RP47) via the SAG Gene
Sanger Sequencing
$910
Sequencing with CNV
PGxome
$890
Oligodontia-Colorectal Cancer via the AXIN2 Gene
Sequencing with CNV
PG-Select
$640
Oocyte Maturation Defect (OOMD) via the ZP1 Gene
Sanger Sequencing
$940
Sequencing with CNV
PGxome
$890
Opitz G/BBB Syndrome Type 1 via the MID1 Gene
Sanger Sequencing
$870
Sequencing with CNV
PGxome
$890
Optic Atrophy 7 (OPA7) via the TMEM126A Gene
Sanger Sequencing
$540
Sequencing with CNV
PGxome
$890
Optic Atrophy and Hereditary Spastic Paraplegia via the SPG7 Gene
Sanger Sequencing
$990
Sequencing with CNV
PGxome
$890
Ornithine Transcarbamylase Deficiency via the OTC Gene
Sanger Sequencing
$840
Sequencing with CNV
PGxome
$930
Orotic Aciduria via the UMPS Gene
Sanger Sequencing
$750
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the BMP1 Gene
Sanger Sequencing
$1130
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the COL1A1 Gene
Sequencing with CNV
PG-Select
$640
Osteogenesis Imperfecta via the COL1A2 Gene
Sequencing with CNV
PG-Select
$640
Osteogenesis Imperfecta via the CRTAP Gene
Sanger Sequencing
$710
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the FKBP10 Gene
Sanger Sequencing
$840
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the IFITM5 Gene
Sanger Sequencing
$440
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the P3H1 / LEPRE1 Gene
Sanger Sequencing
$870
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the SERPINF1 Gene
Sanger Sequencing
$680
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the SERPINH1 Gene
Sanger Sequencing
$650
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the SP7 Gene
Sanger Sequencing
$610
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the TMEM38B Gene
Sanger Sequencing
$650
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta via the WNT1 Gene
Sanger Sequencing
$580
Sequencing with CNV
PGxome
$890
Osteogenesis Imperfecta-Bruck Syndrome Type II via the PLOD2 Gene
Sanger Sequencing
$1190
Sequencing with CNV
PGxome
$890
Osteopetrosis via the CA2 Gene
Sanger Sequencing
$810
Sequencing with CNV
PGxome
$890
Osteopetrosis via the CLCN7 Gene
Sanger Sequencing
$1250
Sequencing with CNV
PGxome
$890
Osteopetrosis via the OSTM1 Gene
Sanger Sequencing
$610
Sequencing with CNV
PGxome
$890
Osteopetrosis via the SNX10 Gene
Sanger Sequencing
$650
Sequencing with CNV
PGxome
$890
Osteopetrosis via the TCIRG1 Gene
Sequencing with CNV
PG-Select
$640
Osteopetrosis via the TNFSF11 Gene
Sanger Sequencing
$540
Sequencing with CNV
PGxome
$890
Otopalatodigital Spectrum Disorders, Periventricular Nodular Heterotopia and Cardiac Valvular Dystrophy via the FLNA Gene
Sequencing with CNV
PG-Select
$640
Ovarian Cancer and Rhabdoid Tumor Predisposition Syndrome via the SMARCA4 Gene
Sequencing with CNV
PG-Select
$640
Ovarian Dysgenesis and Ovarian Hyperstimulation Syndrome via the FSHR Gene
Sanger Sequencing
$860
Sequencing with CNV
PGxome
$890
Ovarian Dysgenesis via the BMP15 Gene
Sanger Sequencing
$490
Sequencing with CNV
PGxome
$890
  • GO BACK
    Test By Category
  • View All Tests
  • View All Panels
ORDER
Test Kits
START
Custom Panel

METHOD KEY

  • Sequencing with CNV
    PGxome
  • Sequencing with CNV
    PG-Select
  • CNV via aCGH
  • Sanger Sequencing
  • MLPA
  • Repeat Expansion
  • Other
Privacy Practices & Policies | Terms & Conditions | Contact Us | Careers | Sign up for Newsletter
Also of Interest:
  • Category
  • PGxome ® - Whole Exome Sequencing
  • TESTS BY DISEASE

© 2021 PreventionGenetics. All rights reserved.

Tweets by PrevGenetics

Put us to the test

We use cookies and tracking to improve your browsing experience on our website, to analyze our website traffic, and to understand where our visitors are coming from. By browsing our website, you consent to this.