Search Tests - PreventionGenetics

Menu

Menu
  • Testing

      Test Menu

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

      Test Information

      • Test Methods
      • Variant Interpretation
      • Family Testing
      • Re-analysis Policy
      • Extract and Hold
  • Sponsored Testing

      Partner Programs

      • Collaboration
      • Sponsored Testing
      • Clinical Trials and Research Studies
  • Billing

      Billing Information

      • Billing Policy
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • 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
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Genetics Experts
      • Quality & Value
      • Publications
      • Licenses and Certificates
      • Webinars
      • 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
      • PGmax
      • Custom Panels
      • Tests by Category
      • How To Order
      • Targeted Variants
      • Prenatal
      • All Tests
      • Tests by Disease

      Test Information

      • Test Methods
      • Variant Interpretation
      • Family Testing
      • Re-analysis Policy
      • Extract and Hold
  • |
  • Sponsored Testing

      Partner Programs

      • Collaboration
      • Sponsored Testing
      • Clinical Trials and Research Studies
  • |
  • Billing

      Billing Information

      • Billing Policy
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • |
  • 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
  • |
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Genetics Experts
      • Quality & Value
      • Publications
      • Licenses and Certificates
      • Webinars
      • 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: 3209

Search Results

  • DNA in a shopping cart TNXB-Related Disorders via the TNXB Gene, Exons 32-44
    Test Code
    Method
    Price
    6088
    Sanger Sequencing
    $530
  • DNA in a shopping cart Nemaline Myopathy 9 via the KLHL41 Gene
    Test Code
    Method
    Price
    11435
    Sequencing with CNV PGxome
    $990
    327
    Sanger Sequencing
    $750
  • DNA in a shopping cart Deafness, Autosomal Recessive 9 (DFNB9) via the OTOF Gene
    Test Code
    Method
    Price
    11549
    Sequencing with CNV PGxome
    $990
    1894
    Sanger Sequencing
    $2170
  • DNA in a shopping cart Cataract 9, Multiple Types (CTRCT9) via the CRYAA Gene
    Test Code
    Method
    Price
    2901
    Sanger Sequencing
    $490
    3879
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Lethal Congenital Contracture Syndrome 9 via the ADGRG6 Gene
    Test Code
    Method
    Price
    15443
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Holoprosencephaly-9 (Autosomal Dominant, Nonsyndromic) via the GLI2 Gene
    Test Code
    Method
    Price
    11355
    Sequencing with CNV PGxome
    $990
    586
    Sanger Sequencing
    $1080
  • DNA in a shopping cart Hermansky-Pudlak Syndrome Type 9 (HPS9) via the BLOC1S6/PLDN Gene
    Test Code
    Method
    Price
    758
    Sanger Sequencing
    $610
    8749
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Deafness, Autosomal Dominant 9 (DFNA9) and Autosomal Recessive Hearing Loss via the COCH Gene
    Test Code
    Method
    Price
    11185
    Sequencing with CNV PGxome
    $990
    1892
    Sanger Sequencing
    $870
  • DNA in a shopping cart Catecholaminergic Polymorphic Ventricular Tachycardia via the CASQ2 Gene
    Test Code
    Method
    Price
    11139
    Sequencing with CNV PGxome
    $990
    941
    Sanger Sequencing
    $770
  • DNA in a shopping cart DICER1 Syndrome via the DICER1 Gene
    Test Code
    Method
    Price
    3041
    Sequencing with CNV PG-Select
    $990
  • DNA in a shopping cart Hereditary Leiomyomatosis and Renal Cell Cancer or Fumarase Deficiency via the FH Gene
    Test Code
    Method
    Price
    7647
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Nephronophthisis via the NPHP4 Gene
    Test Code
    Method
    Price
    15265
    Sequencing with CNV PG-Select
    $990
  • DNA in a shopping cart Bardet-Biedl Syndrome via the TRIM32/BBS11 Gene
    Test Code
    Method
    Price
    15209
    Sequencing with CNV PG-Select
    $990
  • DNA in a shopping cart Hereditary Hemorrhagic Telangiectasia Type 2 (HHT2) via the ACVRL1/ALK1 Gene
    Test Code
    Method
    Price
    11065
    Sequencing with CNV PGxome
    $990
    862
    Sanger Sequencing
    $770
  • DNA in a shopping cart Hereditary Hemorrhagic Telangiectasia Type 1 (HHT1) / Osler-Weber-Rendu Disease via the ENG Gene
    Test Code
    Method
    Price
    11289
    Sequencing with CNV PGxome
    $990
    861
    Sanger Sequencing
    $990
  • DNA in a shopping cart Hyperammonemia via the NAGS Gene
    Test Code
    Method
    Price
    555
    Sanger Sequencing
    $650
    9711
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Medium Chain Acyl-CoA Dehydrogenase Deficiency via the ACADM Gene
    Test Code
    Method
    Price
    180
    Sanger Sequencing
    $750
    9505
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Agnathia-Otocephaly Complex via the PRRX1 Gene
    Test Code
    Method
    Price
    1298
    Sanger Sequencing
    $580
    8827
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Cataract 17, Multiple Types (CTRCT17) via the CRYBB1 Gene
    Test Code
    Method
    Price
    2903
    Sanger Sequencing
    $580
    3885
    Sequencing with CNV PGxome
    $990
  • Mirum Pharmaceuticals Early-Onset Bilateral Cataracts Sponsored Testing

    …Sensitivity Whole exome sequencing identified pathogenic variants in 9 probands from 23 pedigrees affected by familial dominant cataracts (39%) in several congenital or early-onset cataract genes (Reis et al. 2013). In another study…

1 2 3 4 5 6 7 8 9 10 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

© 2025 PreventionGenetics. All rights reserved.

Quick links

Privacy Practices & Policies
HIPAA Compliance
Do Not Sell
Contact Us
Careers
Get on Our Mailing List

Follow us on