U.S. flag

An official website of the United States government

Filters

Test type

Test purpose

Test method

Test service

Laboratory certification

Specimen type

See more specimen types...

Laboratory location

See more states

Other countries

See more countries
  • Showing results for proton polyandrus. Your search for Croton polyandrus retrieved no results.

Results: 1 to 20 of 32

Tests names and labsConditionsGenes, analytes, and microbesMethods

Psych HealthPGx Panel

RPRD Diagnostics, LLC
United States
4013
  • D Deletion/duplication analysis
  • T Targeted variant analysis

CYP2C19 Genotyping

Sanford Medical Genetics Laboratory Sanfordhealth
United States
121
  • T Targeted variant analysis

Gravity Pharmacogenetics Comprehensive Profile

Gravity Diagnostics
United States
8617
  • T Targeted variant analysis

CYP2C19 Genotype

Mayo Clinic Laboratories Mayo Clinic
United States
121
  • T Targeted variant analysis

CYP2C19 Rapid Genotyping Test

RPRD Diagnostics, LLC
United States
1112
  • T Targeted variant analysis

Mitochondrial genome sequencing

Molecular Vision Laboratory
United States
526339
  • C Sequence analysis of the entire coding region

TMEM206 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NGS Panel for Iron related Anemias (including Aceruloplasminemia, Atransferrinemia, IRIDA, DMT1-deficiency =AHMIO1, Hypochromic microcytic anemia with iron overload 2=AHMIO2)

BloodGenetics
Spain
99
  • C Sequence analysis of the entire coding region

HemeZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine
United States
10796
  • C Sequence analysis of the entire coding region

Invitae Iron Related Disorders Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
3927
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Anemia, hypochromic microcytic, with iron overload 1, 206100, Autosomal recessive; AHMIO1 (Microcytic anemia with liver iron overload) (SLC11A2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

WES iron disorders

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
2046
  • E Sequence analysis of select exons

panel microcytic anemia-due to iron disorder (SLC11A2, TMPRSS6, TF, CP)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
44
  • C Sequence analysis of the entire coding region

SLC11A2 - hypochromic microcytic anemia

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

Haematological diseases panel _v.2.0

CGC Genetics Unilabs
Portugal
1344
  • C Sequence analysis of the entire coding region

Anemia Panel

CGC Genetics Unilabs
Portugal
1174
  • C Sequence analysis of the entire coding region

Microcytic anemia with liver iron overload (sequence analysis of SLC11A2 gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Hereditary Anemias Panel

Mendelics
Brazil
1183
  • C Sequence analysis of the entire coding region

HEREDITARY ANEMIAS EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1144
  • E Sequence analysis of select exons

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 32

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.