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

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

      Test Information

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

      Education

      • 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
      • Licenses and Certificates
      • PGNewsroom
      • Join Our Team
  • 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

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

      Test Information

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

      Education

      • 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
      • 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?

×
  • Test By Category
  • View All Tests
  • View All Panels

FILTERS

ORDER
Test Kits

RESULTS KEY

  • Tests & Panels
  • Categories
  • Newsroom
  • Custom panels
  • Pages & Documents
  • Webinars

Searched: Progressive Familial Intrahepatic Cholestasis (PFIC) and Alagille syndrome Sequencing Panel

Search Results

  • DNA in a shopping cart Familial Limb Girdle Myasthenic Syndrome via the AGRN Gene
    Test Code
    Method
    Price
    11077
    Sequencing with CNV PGxome
    $890
    408
    Sanger Sequencing
    $1750
  • DNA in a shopping cart Familial Cold Autoinflammatory Syndrome 2 via the NLRP12 Gene
    Test Code
    Method
    Price
    11517
    Sequencing with CNV PGxome
    $890
    2067
    Sanger Sequencing
    $1020
  • DNA in a shopping cart Seckel Syndrome, Primary Microcephaly and Familial Cutaneous Telangiectasia and Cancer Syndrome via the ATR Gene
    Test Code
    Method
    Price
    7979
    Sequencing with CNV PGxome
    $890
    1291
    Sanger Sequencing
    $2450
  • DNA in a shopping cart Familial Episodic Pain Type 2 Syndrome via the SCN10A Gene
    Test Code
    Method
    Price
    11639
    Sequencing with CNV PGxome
    $890
    1795
    Sanger Sequencing
    $1620
  • Documents - Nicudisorder List

    ……

  • DNA in a shopping cart Hereditary Cystic Kidney Diseases Panel
    Test Code
    Method
    Price
    10619
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel
    Test Code
    Method
    Price
    15423
    Sequencing with CNV PGxome
    $1380
  • DNA in a shopping cart Comprehensive Ocular Disorders Panel
    Test Code
    Method
    Price
    12005
    Sequencing with CNV PGxome
    $1190
  • News Genetic Testing for Congenital Heart Disease

    ……

  • DNA in a shopping cart Early-Onset High Myopia Panel
    Test Code
    Method
    Price
    15487
    Sequencing with CNV PGxome
    $1240
  • DNA in a shopping cart Congenital Bile Acid Synthesis Defect Type 1 via the HSD3B7 Gene
    Test Code
    Method
    Price
    15249
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Congenital Bile Acid Synthesis Defect Type 2 via the AKR1D1 Gene
    Test Code
    Method
    Price
    15223
    Sequencing with CNV PG-Select
    $640
  • Panels

    ……

  • Panels

    ……

  • DNA in a shopping cart Brown-Vialetto-Van Laere Syndrome 2 and Fazio-Londe Disease (Progressive Bulbar Palsy with or without Sensorineural Deafness) via the SLC52A2 Gene
    Test Code
    Method
    Price
    920
    Sanger Sequencing
    $440
    9167
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Brown-Vialetto-Van Laere Syndrome 1 and Fazio-Londe Disease (Progressive Bulbar Palsy With or Without Sensorineural Deafness) via the SLC52A3 Gene
    Test Code
    Method
    Price
    8711
    Sequencing with CNV PGxome
    $890
    417
    Sanger Sequencing
    $630
  • DNA in a shopping cart Epilepsy and Seizure Panel
    Test Code
    Method
    Price
    7347
    Sequencing with CNV PGxome
    $1490
  • DNA in a shopping cart Skeletal Disorders and Joint Problems Panel
    Test Code
    Method
    Price
    10631
    Sequencing with CNV PGxome
    $1790
  • DNA in a shopping cart Isolated Polycystic Liver Disease (PCLD) Panel
    Test Code
    Method
    Price
    10135
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Comprehensive Movement Disorders Panel
    Test Code
    Method
    Price
    16004
    Sequencing with CNV PGxome
    $1490
Previous 1 ... 3 4 5 6 7 8 9 10 11 12 Next
  • GO BACK
    Test By Category
  • View All Tests
  • View All Panels
ORDER
Test Kits
Custom Panel CogSTART
Custom Panel

RESULTS KEY

  • Tests & Panels
  • Categories
  • Newsroom
  • Custom panels
  • Pages & Documents
  • Webinars

PreventionGenetics,
A wholly owned subsidiary of Exact Sciences Corp.

3800 S. Business Park Ave.
Marshfield, WI 54449
Contact Us

© 2023 PreventionGenetics. All rights reserved.

Quick links

Privacy Practices & Policies
Terms & Conditions
Contact Us
Careers
Sign Up For Newsletter

Follow us on

Also of Interest:
  • Genetic Tests by Category
  • PGxome ® - Whole Exome Sequencing
  • Genetic Tests by Disease
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.