NSW Health Pathology

Site

NSW Health Pathology Randwick Genetics Branch Laboratory

Accreditation No.

2206

Site No.

26036

Date of Accreditation

25 Nov 2025

Address

Level 5, Margarete Ainsworth Building, 139 Barker Street
Randwick, NSW 2031
Australia

pathology.health.nsw.gov.au

Contact

Availability

Services available to external clients

Supervision

GY (General)

NSW Health Pathology address map

Scope of Accreditation

Print scopes
NSW Health Pathology Randwick Genetics Branch Laboratory

ISO 15189 (2022)

Human Pathology

  • This facility complies with the relevant National Pathology Accreditation Advisory Council (NPAAC) requirements.
Service Product Determinant
Cytogenetics - Molecular karyotype (SNP microarray) detection of unbalanced chromosome abnormalitiesAnalysis and Reporting only Amniotic fluid; Blood; Bone marrow aspirate; Chorionic villus tissue; Other body fluids; Other tissues - Non-malignant Absence of heterozygosity; Cytogenetic analysis and reporting; Pathogenic copy number changes
Amniotic fluid; Blood; Bone marrow; Chorionic villus tissue; Other body fluids; Other tissues - Non-malignant Cytogenetic analysis and reporting; Pathogenic copy number changes
Cytogenetics - Molecular karyotype (SNP microarray) detection of unbalanced chromosome abnormalitiesReporting only Blood DNA methylation episignatures
Molecular genetics - Investigation of constitutional genetic variants - Carrier testing - Targeted genesAnalysis and reporting only Amniotic fluid; Blood; Chorionic villus; Saliva Ashkenazi Jewish; Craniosynostosis; Cystic fibrosis
Molecular genetics - Investigation of constitutional genetic variants - Carrier testing - Whole genome sequencing studies for inherited (germline) DNA/RNA changesAnalysis and reporting only Amniotic fluid; Blood; Chorionic villus; Extracted DNA; Mouth swabs; Products of conception (POC); Saliva; Tissues Copy number variation (CNV); Indels; Single nucleotide variants (SNVs); Structural variations (SVs)
Molecular genetics - Investigation of constitutional genetic variants - Diagnostic testing - Whole exome sequencing studies for inherited (germline) DNA/RNA changesAnalysis and reporting only Amniotic fluid; Blood; Chorionic villus; Extracted DNA; Mouth swabs; Products of conception (POC); Saliva; Tissues Copy number variation (CNV); Medical exome
Blood Copy number variation (CNV); Medical exome
Molecular genetics - Investigation of constitutional genetic variants - Diagnostic testing - Whole genome sequencing studies for inherited (germline) DNA/RNA changesAnalysis and reporting only Amniotic fluid; Blood; Chorionic villus; Extracted DNA; Mouth swabs; Products of conception (POC); Saliva; Tissues Copy number variation (CNV); Indels; Single nucleotide variants (SNVs); Structural variations (SVs)
Molecular genetics - Prenatal genetic testing (excluding non-invasive prenatal [genetic] screening)Analysis and reporting only Amniotic fluid; Blood; Chorionic villus Craniosynostosis; Veno-occlusive disease with immunodeficiency; β-Thalassaemia
Duchenne-Becker muscular dystrophy
Molecular genetics - Screening for an unknown mutation - Whole genome sequencing studies for inherited (germline) DNA/RNA changesAnalysis and reporting only Amniotic fluid; Blood; Chorionic villus; Extracted DNA; Mouth swabs; Products of conception (POC); Saliva; Tissues Copy number variation (CNV); Indels; Single nucleotide variants (SNVs); Structural variations (SVs)
Molecular genetics/Cytogenetics - Bioinformatic analysis DNA sequences Primary analysis - Conversion of instrument file to FASTQ or FASTA file; Secondary analysis - Alignment and variant calling; Tertiary analysis - Data annotation and interpretation

The only data displayed is that deemed relevant and necessary for the clear description of the activities and services covered by the scope of accreditation.

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