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Fanconi anemia complementation group C
Synonyms: FACC; FANCONI PANCYTOPENIA, TYPE 3; Fanconi anemia, group C
Gene: FANCC

Labs matching your search

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31 labs with tests matching your search
Lab name Tests matching your search
ARUP Laboratories, Molecular Genetics and Genomics United States2
Baylor Genetics United States3
Bioarray Spain1
BloodGenetics Spain2
CEN4GEN Institute for Genomics and Molecular Diagnostics Canada1
CNH Molecular Diagnostics Laboratory United States2
CeGaT GmbH Germany2
Center for Human Genetics, Inc United States1
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory United States5
Fulgent Genetics United States17
GeneID Lab - Advanced Molecular Diagnostics United States1
Genesys Diagnostics United States5
Genetic Services Laboratory United States1
Genome Diagnostics Laboratory Canada1
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics United States1
HNL Genomics Connective Tissue Gene Tests United States2
Intergen Genetics and Rare Diseases Diagnosis Center Turkey2
Johns Hopkins Genomics DNA Diagnostic Laboratory United States1
Knight Diagnostic Laboratories - Molecular Diagnostic Center United States1
Labcorp Genetics (formerly Invitae) United States3
MNG Laboratories (Medical Neurogenetics, LLC.) United States1
Molecular Diagnostic Laboratory United States2
Molecular Genetics Laboratory Canada1
Myriad Genetics, Inc. United States1
Natera, Inc. United States11
NxGen MDx United States4
Precision Medicine Care (PMC®) United States1
PreventionGenetics, part of Exact Sciences United States6
Quantitative Genomic Medicine Laboratories, SL Spain1
Quest Diagnostics Nichols Institute Chantilly United States2
Quest Diagnostics Nichols Institute San Juan Capistrano United States1
Results:
85 genetic tests from 31 labs with tests matching your search
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Fanconi anemia, complementation group C, 227645, Autosomal recessive; FANCC (Fanconi anemia) (FANCC gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Fanconi anemia, complementation group C, 227645, Autosomal recessive; FANCC (Fanconi anemia) (FANCC gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

RenaDx™: Comprehensive Renal Disease Genetics Panel

Precision Medicine Care (PMC®)
United States
468448
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cancer Screening - Breast Cancer Panel (19 Genes)

Genesys Diagnostics, Genesys Diagnostics, Inc.
United States
2219
  • X Mutation scanning of select exons

Hereditary Cancer Screening - Colorectal & Gastric Cancer Panel (including Pancreatic Cancer) - (43 Genes)

Genesys Diagnostics, Genesys Diagnostics, Inc.
United States
5843
  • X Mutation scanning of select exons

Hereditary Cancer Screening - Breast & Gynecological Cancer Panel (33 Genes)

Genesys Diagnostics, Genesys Diagnostics, Inc.
United States
3733
  • X Mutation scanning of select exons

Hereditary Cancer Screening - Full Hereditary Cancer Panel (99 Genes)

Genesys Diagnostics, Genesys Diagnostics, Inc.
United States
10999
  • X Mutation scanning of select exons

Carrier Screening - Comprehensive Panel (145 Genes)

Genesys Diagnostics, Genesys Diagnostics, Inc.
United States
185145
  • D Deletion/duplication analysis
  • I Microsatellite instability testing (MSI)
  • X Mutation scanning of select exons
  • T Targeted variant analysis

NewbornGeneID

GeneID Lab - Advanced Molecular Diagnostics
United States
7361
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NGS Panel for Fanconi anemia

BloodGenetics
Spain
2222
  • C Sequence analysis of the entire coding region

NGS Panel for Bone Marrow failure

BloodGenetics
Spain
5669
  • C Sequence analysis of the entire coding region

Invitae Inborn Errors of Immunity and Cytopenias Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
754562
  • D Deletion/duplication analysis

MarrowZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
United States
313228
  • C Sequence analysis of the entire coding region

Fanconi Anemia Type C

Myriad Genetics, Inc.
United States
11
  • C Sequence analysis of the entire coding region

VistaSeq Breast and GYN Cancer Panel

Molecular Diagnostic Laboratory, LabCorp
United States
3225
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
325300
  • C Sequence analysis of the entire coding region

Invitae Bone Marrow Failure Syndromes Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
13785
  • D Deletion/duplication analysis

Fanconi Anemia Panel

Genetic Services Laboratory, University of Chicago
United States
2019
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Fanconi Anemia Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
2615
  • D Deletion/duplication analysis

Fanconi Anemia DNA Mutation Analysis

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
11
  • T Targeted variant analysis
85 tests from 31 labs
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View the list of labs matching your search query.
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❮Page 1 of 5❯
Fanconi anemia, complementation group C, 227645, Autosomal recessive; FANCC (Fanconi anemia) (FANCC gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Fanconi anemia, complementation group C, 227645, Autosomal recessive; FANCC (Fanconi anemia) (FANCC gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
RenaDx™: Comprehensive Renal Disease Genetics Panel by Precision Medicine Care (PMC®)
468 conditions, 448 genes
Hereditary Cancer Screening - Breast Cancer Panel (19 Genes) by Genesys Diagnostics, Genesys Diagnostics, Inc.
22 conditions, 19 genes
Hereditary Cancer Screening - Colorectal & Gastric Cancer Panel (including Pancreatic Cancer) - (43 Genes) by Genesys Diagnostics, Genesys Diagnostics, Inc.
58 conditions, 43 genes
Hereditary Cancer Screening - Breast & Gynecological Cancer Panel (33 Genes) by Genesys Diagnostics, Genesys Diagnostics, Inc.
37 conditions, 33 genes
Hereditary Cancer Screening - Full Hereditary Cancer Panel (99 Genes) by Genesys Diagnostics, Genesys Diagnostics, Inc.
109 conditions, 99 genes
Carrier Screening - Comprehensive Panel (145 Genes) by Genesys Diagnostics, Genesys Diagnostics, Inc.
185 conditions, 145 genes
NewbornGeneID by GeneID Lab - Advanced Molecular Diagnostics
73 conditions, 61 genes
NGS Panel for Fanconi anemia by BloodGenetics
22 conditions, 22 genes
NGS Panel for Bone Marrow failure by BloodGenetics
56 conditions, 69 genes
Invitae Inborn Errors of Immunity and Cytopenias Panel by Labcorp Genetics (formerly Invitae), LabCorp
754 conditions, 562 genes
MarrowZoom by Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
313 conditions, 228 genes
Fanconi Anemia Type C by Myriad Genetics, Inc.
1 condition, 1 gene
VistaSeq Breast and GYN Cancer Panel by Molecular Diagnostic Laboratory, LabCorp
32 conditions, 25 genes
qCarrier Plus by Quantitative Genomic Medicine Laboratories, SL
325 conditions, 300 genes
Invitae Bone Marrow Failure Syndromes Panel by Labcorp Genetics (formerly Invitae), LabCorp
137 conditions, 85 genes
Fanconi Anemia Panel by Genetic Services Laboratory, University of Chicago
20 conditions, 19 genes
Invitae Fanconi Anemia Panel by Labcorp Genetics (formerly Invitae), LabCorp
26 conditions, 15 genes
Fanconi Anemia DNA Mutation Analysis by Quest Diagnostics Nichols Institute San Juan Capistrano
1 condition, 1 gene

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.