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: Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome via the KCNH1 Gene

Search Results

  • DNA in a shopping cart Overgrowth and Macrocephaly Syndromes Panel
    Test Code
    Method
    Price
    3449
    Sequencing with CNV PGxome
    $1290
  • DNA in a shopping cart Congenital Anomalies of the Gastrointestinal Tract Panel
    Test Code
    Method
    Price
    13377
    Sequencing with CNV PGxome
    $1290
  • DNA in a shopping cart Baraitser-Winter Syndrome Type 1 via the ACTB Gene
    Test Code
    Method
    Price
    8835
    Sequencing with CNV PGxome
    $990
    2008
    Sanger Sequencing
    $580
  • DNA in a shopping cart Epilepsy and Seizure Panel
    Test Code
    Method
    Price
    7347
    Sequencing with CNV PGxome
    $1490
  • DNA in a shopping cart Manitoba Oculotrichoanal Syndrome (MOTA) via the FREM1 Exon 8-23 Deletion
    Test Code
    Method
    Price
    3782
    Targeted Deletion
    $350
  • DNA in a shopping cart Floating-Harbor Syndrome via the SRCAP Gene
    Test Code
    Method
    Price
    11715
    Sequencing with CNV PGxome
    $990
    607
    Sanger Sequencing
    $2080
  • DNA in a shopping cart Brain Malformation Panel
    Test Code
    Method
    Price
    12613
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Coffin-Siris Syndrome Panel
    Test Code
    Method
    Price
    10221
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Marinesco-Sjogren Syndrome via the SIL1 Gene
    Test Code
    Method
    Price
    11667
    Sequencing with CNV PGxome
    $990
    1674
    Sanger Sequencing
    $750
  • DNA in a shopping cart Deafness, Autosomal Dominant 20 (DFNA20) via the ACTG1 Gene
    Test Code
    Method
    Price
    2009
    Sanger Sequencing
    $540
    8973
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Timothy Syndrome and Brugada Syndrome via the CACNA1C Gene
    Test Code
    Method
    Price
    11123
    Sequencing with CNV PGxome
    $990
    1012
    Sanger Sequencing
    $2110
  • DNA in a shopping cart Meckel-Gruber Syndrome / Joubert Syndrome via the TCTN2 Gene
    Test Code
    Method
    Price
    576
    Sanger Sequencing
    $1010
    11041
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Sick Sinus Syndrome and Brugada Syndrome via the HCN4 Gene
    Test Code
    Method
    Price
    11369
    Sequencing with CNV PGxome
    $990
    947
    Sanger Sequencing
    $960
  • DNA in a shopping cart Pierson Syndrome and Congenital Nephrotic Syndrome via the LAMB2 Gene
    Test Code
    Method
    Price
    11443
    Sequencing with CNV PGxome
    $990
    556
    Sanger Sequencing
    $1620
  • DNA in a shopping cart Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene
    Test Code
    Method
    Price
    7851
    Sequencing with CNV PG-Select
    $990
  • DNA in a shopping cart Oculofaciocardiodental Syndrome and Lenz Microphthalmia Syndrome via the BCOR Gene
    Test Code
    Method
    Price
    11105
    Sequencing with CNV PGxome
    $990
    949
    Sanger Sequencing
    $1250
  • DNA in a shopping cart Rubinstein-Taybi Syndrome and Floating-Harbor Syndrome Panel
    Test Code
    Method
    Price
    10141
    Sequencing with CNV PGxome
    $990
  • News News

    ……

  • DNA in a shopping cart Comprehensive Brain Malformation Panel
    Test Code
    Method
    Price
    12619
    Sequencing with CNV PGxome
    $1490
  • DNA in a shopping cart Andersen-Tawil Syndrome/Long QT Syndrome via the KCNJ2 Gene
    Test Code
    Method
    Price
    1042
    Sanger Sequencing
    $440
    9163
    Sequencing with CNV PGxome
    $990
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