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Results: 1 to 20 of 39

Tests names and labsConditionsGenes, analytes, and microbesMethods

G-Banded Chromosome Analysis

Cytogenetics Laboratory University Of Washington
United States
166
  • K Karyotyping

Blood chromosome analysis

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
723
  • K Karyotyping

Standard karyotype (pediatric)

Allele Diagnostics
United States
166
  • K Karyotyping

Invitae Surgical Risk Screen

Invitae
United States
248
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

F5 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel

PreventionGenetics, part of Exact Sciences
United States
346160
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Pregnancy loss, recurrent, susceptibility to, 1, 614389, Autosomal dominant; RPRGL1 (F5 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

Pregnancy loss, recurrent, susceptibility to, 1, 614389, Autosomal dominant; RPRGL1 (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Invitae Genetic Health Screen

Invitae
United States
409164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Cardio Screen

Invitae
United States
20881
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Karyotype from Blood

Diagnostics Division CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS
India
151
  • K Karyotyping

Invitae Hereditary Thrombophilia Panel

Invitae
United States
2411
  • D Deletion/duplication analysis

Thrombophilia Mutation Panel

Baylor Genetics
United States
113
  • T Targeted variant analysis

Factor V Leiden Mutation Panel

Baylor Genetics
United States
51
  • S Mutation scanning of the entire coding region

Clotting factor deficiency panel. 16-gene NGS panel.

Genologica Medica
Spain
2916
  • C Sequence analysis of the entire coding region

Bleeding disorder / coagulopathy panel. NGS panel of 62 genes.

Genologica Medica
Spain
9662
  • C Sequence analysis of the entire coding region

Comprehensive Bleeding Disorder Panel

Versiti Diagnostic Laboratories Versiti, Inc
United States
8050
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Female Infertility

Asper Biogene Asper Biogene LLC
Estonia
8564
  • C Sequence analysis of the entire coding region

Chromosome Analysis, Tissue w/ Reflex to Microarray, ClariSure(R) Oligo-SNP

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
21
  • K Karyotyping
  • D Deletion/duplication analysis

Thrombosis Disorder NGS Panel

Fulgent Genetics
United States
4618
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 39

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.