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Results: 1 to 20 of 66

Tests names and labsConditionsGenes, analytes, and microbesMethods

Tempus xT

Tempus AI - RTP
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Pancreatitis SNaP-Shot

Ariel Precision Medicine
United States
1116
  • T Targeted variant analysis

SPINK1 Gene Pancreatitis NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

SPINK1

Department of Clinical Genetics Odense University Hospital
Denmark
11
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Hereditary Pancreatitis Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
14
  • C Sequence analysis of the entire coding region

SPINK1 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pancreatitis Panel

Centogene AG - the Rare Disease Company
Germany
2729
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fibrocalculous pancreatic diabetes, susceptibility to, 608189, Autosomal recessive, Autosomal dominant (Tropical pancreatitis) (SPINK1 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

Fibrocalculous pancreatic diabetes, susceptibility to, 608189, Autosomal recessive, Autosomal dominant (Tropical pancreatitis) (MLPA)

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

Tropical calcific pancreatitis, 608189, Autosomal recessive, Autosomal dominant (Tropical pancreatitis) (MLPA)

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

Tropical calcific pancreatitis, 608189, Autosomal recessive, Autosomal dominant (Tropical pancreatitis) (SPINK1 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

Pancreatitis, hereditary, 167800, Autosomal dominant; PCTT (Hereditary chronic pancreatitis) (SPINK1 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

Pancreatitis, hereditary, 167800, Autosomal dominant; PCTT (Hereditary chronic pancreatitis) (MLPA)

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

Congenital Diarrhea and Enteropathies Panel

PreventionGenetics, part of Exact Sciences
United States
241157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PancNext® plus Pancreatitis

Ambry Genetics
United States
4119
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pancreatitis Panel

Ambry Genetics
United States
66
  • C Sequence analysis of the entire coding region

CustomNext-Cancer®

Ambry Genetics
United States
14691
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pancreatitis: Three-gene Profile (PRSS1, SPINK1, CFTR) (Full Gene Sequencing)

Molecular Diagnostic Laboratory LabCorp
United States
13
  • C Sequence analysis of the entire coding region

Pancreatitis: SPINK1 (Known Mutation)

Molecular Diagnostic Laboratory LabCorp
United States
11
  • E Sequence analysis of select exons

Pancreatitis: SPINK1 (Full Gene Sequencing)

Molecular Diagnostic Laboratory LabCorp
United States
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 66

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.