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GTR Home > Laboratories > Natera, Inc.

Natera, Inc.

GTR Lab ID: 500034, Last updated:2022-01-25

Personnel

  • Director: J. Dianne Keen-Kim, PhD, ABMG, FACMG, DABMG, Lab Director
    Phone: 6502499090
    Email: support@natera.com
  • Jennifer Saucier, MS, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 650-249-9090
    Fax: 650-730-2276
    Email: jsaucier@natera.com

Conditions and tests

  • 22q partial monosomy1 test
  • 3 beta-Hydroxysteroid dehydrogenase deficiency4 tests
  • 3-methylcrotonyl-CoA carboxylase 1 deficiency4 tests
  • 3-methylcrotonyl-CoA carboxylase 2 deficiency4 tests
  • 3-Methylglutaconic aciduria type 36 tests
  • 3-phosphoglycerate dehydrogenase deficiency9 tests
  • 5p partial monosomy syndrome1 test
  • 6-Pyruvoyl-tetrahydrobiopterin synthase deficiency7 tests
  • Abetalipoproteinaemia9 tests
  • Achondrogenesis, type IB7 tests
  • Achromatopsia 34 tests
  • Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins6 tests
  • Acyl-CoA dehydrogenase 9 deficiency4 tests
  • Acyl-CoA oxidase deficiency4 tests
  • Adrenoleukodystrophy7 tests
  • Agenesis of the corpus callosum with peripheral neuropathy7 tests
  • Aicardi Goutieres syndrome4 tests
  • alpha Thalassemia16 tests
  • Alpha thalassemia-intellectual disability syndrome type 13 tests
  • Alstrom syndrome4 tests
  • Angelman syndrome1 test
  • Anomaly of sex chromosome2 tests
  • Argininosuccinate lyase deficiency7 tests
  • Aromatase deficiency4 tests
  • Aspartylglucosaminuria7 tests
  • Ataxia-telangiectasia syndrome9 tests
  • Autism spectrum disorder - epilepsy - arthrogryposis syndrome9 tests
  • Autosomal chromosomal disorder2 tests
  • Autosomal dominant Alport syndrome9 tests
  • Autosomal recessive congenital ichthyosis 17 tests
  • Autosomal recessive DOPA responsive dystonia7 tests
  • Autosomal recessive limb-girdle muscular dystrophy type 2A7 tests
  • Autosomal recessive limb-girdle muscular dystrophy type 2B6 tests
  • Autosomal recessive limb-girdle muscular dystrophy type 2D7 tests
  • Autosomal recessive limb-girdle muscular dystrophy type 2E7 tests
  • Autosomal recessive limb-girdle muscular dystrophy type 2I4 tests
  • Autosomal recessive nonsyndromic hearing loss 776 tests
  • Autosomal recessive osteopetrosis 14 tests
  • Autosomal recessive polycystic kidney disease16 tests
  • Bardet-Biedl syndrome 17 tests
  • Bardet-Biedl syndrome 107 tests
  • Bardet-Biedl syndrome 124 tests
  • Bardet-Biedl syndrome 25 tests
  • Bare lymphocyte syndrome type 2, complementation group A4 tests
  • Bartter syndrome4 tests
  • Becker muscular dystrophy22 tests
  • Bifunctional peroxisomal enzyme deficiency7 tests
  • Bilateral frontoparietal polymicrogyria4 tests
  • Biotinidase deficiency7 tests
  • Bloom syndrome11 tests
  • Carnitine palmitoyl transferase 1A deficiency7 tests
  • Carnitine palmitoyltransferase II deficiency9 tests
  • Carpenter syndrome4 tests
  • Ceroid lipofuscinosis, neuronal, 6A7 tests
  • Charcot-Marie-Tooth disease3 tests
  • Charcot-Marie-Tooth disease type 4D4 tests
  • Charlevoix-Saguenay spastic ataxia3 tests
  • Cholestanol storage disease9 tests
  • Chorea-acanthocytosis6 tests
  • Choroideremia3 tests
  • Chromosome 1p36 deletion syndrome1 test
  • Chronic granulomatous disease, autosomal, due to deficiency of CYBA6 tests
  • Ciliopathy4 tests
  • Citrin deficiency7 tests
  • Citrullinemia type I11 tests
  • Classic homocystinuria7 tests
  • Cobalamin C disease11 tests
  • Cohen syndrome4 tests
  • Combined malonic and methylmalonic acidemia4 tests
  • Complete trisomy 13 syndrome1 test
  • Complete trisomy 18 syndrome1 test
  • Complete trisomy 21 syndrome1 test
  • Congenital amegakaryocytic thrombocytopenia9 tests
  • Congenital chromosomal disease1 test
  • Congenital disorder of glycosylation type 1C4 tests
  • Congenital disorder of glycosylation type I2 tests
  • Congenital hyperammonemia, type I4 tests
  • Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type7 tests
  • Congenital lipoid adrenal hyperplasia due to STAR deficency4 tests
  • Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome6 tests
  • Congenital myasthenic syndrome 4C9 tests
  • Congenital neutropenia-myelofibrosis-nephromegaly syndrome4 tests
  • Corneal dystrophy-perceptive deafness syndrome4 tests
  • Corticosterone 18-monooxygenase deficiency6 tests
  • Corticosterone methyloxidase type 2 deficiency6 tests
  • Creatine transporter deficiency3 tests
  • Cystic fibrosis32 tests
  • Cystinosis9 tests
  • Decreased plasma carnitine7 tests
  • Deficiency of acetyl-CoA acetyltransferase4 tests
  • Deficiency of alpha-mannosidase7 tests
  • Deficiency of galactokinase4 tests
  • Deficiency of guanidinoacetate methyltransferase4 tests
  • Deficiency of hyaluronoglucosaminidase4 tests
  • Deficiency of hydroxymethylglutaryl-CoA lyase7 tests
  • Deficiency of steroid 17-alpha-monooxygenase4 tests
  • Diabetes insipidus, nephrogenic, autosomal4 tests
  • Dizygotic twins1 test
  • Duchenne muscular dystrophy22 tests
  • Dyskeratosis congenita, autosomal recessive 57 tests
  • Ehlers-Danlos syndrome, dermatosparaxis type9 tests
  • Ellis-van Creveld syndrome4 tests
  • Enhanced S-cone syndrome6 tests
  • Epidermolysis bullosa dystrophica4 tests
  • Ethylmalonic encephalopathy7 tests
  • Fabry disease3 tests
  • Familial dysautonomia16 tests
  • Familial hypercholesterolemia1 test
  • Familial hypokalemia-hypomagnesemia4 tests
  • Familial isolated deficiency of vitamin E7 tests
  • Familial Mediterranean fever6 tests
  • Fanconi anemia complementation group A6 tests
  • Fanconi anemia complementation group C11 tests
  • Fanconi anemia complementation group G4 tests
  • Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 34 tests
  • Finnish congenital nephrotic syndrome7 tests
  • Fragile X syndrome16 tests
  • Fumarase deficiency7 tests
  • Galactosemia16 tests
  • Galactosylceramide beta-galactosidase deficiency7 tests
  • Gaucher disease16 tests
  • Glucose-6-phosphate transport defect7 tests
  • Glutaric acidemia IIa4 tests
  • Glutaric acidemia IIc4 tests
  • Glutaric aciduria, type 17 tests
  • Glycogen storage disease due to glucose-6-phosphatase deficiency type IA11 tests
  • Glycogen storage disease type III9 tests
  • Glycogen storage disease, type II9 tests
  • Glycogen storage disease, type IV6 tests
  • Glycogen storage disease, type V6 tests
  • Glycogen storage disease, type VII6 tests
  • GM1 gangliosidosis7 tests
  • GNE myopathy9 tests
  • GRACILE syndrome7 tests
  • Granulomatous disease, chronic, X-linked6 tests
  • Hemochromatosis type 2A4 tests
  • Hemochromatosis type 34 tests
  • Hemoglobinopathy16 tests
  • Hepatoencephalopathy due to combined oxidative phosphorylation defect type 14 tests
  • Hereditary acrodermatitis enteropathica4 tests
  • Hereditary disease1 test
  • Hereditary factor IX deficiency disease3 tests
  • Hereditary factor XI deficiency disease6 tests
  • Hereditary fructosuria7 tests
  • Hereditary insensitivity to pain with anhidrosis6 tests
  • Hereditary spastic paraplegia 496 tests
  • Hermansky-Pudlak syndrome 14 tests
  • Hermansky-Pudlak syndrome 39 tests
  • Histiocytic medullary reticulosis6 tests
  • Holocarboxylase synthetase deficiency4 tests
  • Homocystinuria due to MTHFR deficiency6 tests
  • Hydrolethalus syndrome4 tests
  • Hyperammonemia, type III4 tests
  • Hypercholesterolemia, familial, 15 tests
  • Hypercholesterolemia, familial, 44 tests
  • Hyperinsulinemic hypoglycemia, familial, 19 tests
  • Hyperinsulinemic hypoglycemia, familial, 24 tests
  • Hyperlipoproteinemia, type I4 tests
  • Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome7 tests
  • Hypohidrotic X-linked ectodermal dysplasia3 tests
  • Hypophosphatasia7 tests
  • Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly4 tests
  • Isolated microphthalmia 26 tests
  • Isovaleryl-CoA dehydrogenase deficiency11 tests
  • Joubert syndrome 29 tests
  • Juvenile retinoschisis3 tests
  • Kartagener syndrome6 tests
  • Kidney Transplant Rejection1 test
  • Kostmann syndrome4 tests
  • Leber congenital amaurosis4 tests
  • Leber congenital amaurosis 26 tests
  • Lethal congenital contracture syndrome 14 tests
  • Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency7 tests
  • Lysinuric protein intolerance7 tests
  • Maple syrup urine disease type 1A7 tests
  • Maple syrup urine disease type 1B9 tests
  • Meckel syndrome, type 14 tests
  • Meckel syndrome, type 29 tests
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency16 tests
  • Megalencephalic leukoencephalopathy with subcortical cysts9 tests
  • Menkes kinky-hair syndrome3 tests
  • Metachromatic leukodystrophy9 tests
  • Metaphyseal chondrodysplasia, McKusick type7 tests
  • Methylcobalamin deficiency type cblE4 tests
  • Methylmalonic aciduria and homocystinuria type cblD4 tests
  • Methylmalonic aciduria, cblA type4 tests
  • Methylmalonic aciduria, cblB type4 tests
  • METHYLMALONIC ACIDURIA, mut(0) TYPE4 tests
  • Microcephaly, normal intelligence and immunodeficiency7 tests
  • Miscarriage1 test
  • Mitochondrial complex I deficiency6 tests
  • Mitochondrial neurogastrointestinal encephalomyopathy6 tests
  • MPI-CDG7 tests
  • Mucolipidosis type III gamma4 tests
  • Mucolipidosis type IV11 tests
  • Mucopolysaccharidosis type 111 tests
  • Mucopolysaccharidosis type 64 tests
  • Mucopolysaccharidosis, MPS-II3 tests
  • Mucopolysaccharidosis, MPS-III-A7 tests
  • Mucopolysaccharidosis, MPS-III-B4 tests
  • Mucopolysaccharidosis, MPS-III-C4 tests
  • Mucopolysaccharidosis, MPS-III-D4 tests
  • Mucopolysaccharidosis, MPS-IV-B7 tests
  • Multiple congenital anomalies1 test
  • Multiple sulfatase deficiency9 tests
  • Muscle eye brain disease7 tests
  • Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 49 tests
  • Myopathy, lactic acidosis, and sideroblastic anemia6 tests
  • Navajo neurohepatopathy4 tests
  • Nemaline myopathy9 tests
  • Nephrotic syndrome, type 27 tests
  • Neuronal ceroid lipofuscinosis 17 tests
  • Neuronal ceroid lipofuscinosis 27 tests
  • Neuronal ceroid lipofuscinosis 311 tests
  • Neuronal ceroid lipofuscinosis 57 tests
  • Neuronal ceroid lipofuscinosis 74 tests
  • Neuronal ceroid lipofuscinosis 87 tests
  • Niemann-Pick disease, type A11 tests
  • Niemann-Pick disease, type C17 tests
  • Niemann-Pick disease, type C24 tests
  • Niemann-Pick disease, type D7 tests
  • Non-acquired combined pituitary hormone deficiency with spine abnormalities4 tests
  • Non-ketotic hyperglycinemia7 tests
  • Nonsyndromic Deafness9 tests
  • Ornithine aminotransferase deficiency6 tests
  • Ornithine carbamoyltransferase deficiency6 tests
  • Pendred syndrome7 tests
  • Peroxisome biogenesis disorder11 tests
  • Phenylketonuria9 tests
  • Pituitary hormone deficiency, combined, 27 tests
  • PMM2-CDG7 tests
  • Polyglandular autoimmune syndrome, type 16 tests
  • Pontocerebellar hypoplasia type 1A6 tests
  • Pontocerebellar hypoplasia type 2D6 tests
  • Pontocerebellar hypoplasia type 66 tests
  • Prader-Willi syndrome1 test
  • Primary ciliary dyskinesia 36 tests
  • Primary ciliary dyskinesia 96 tests
  • Primary hyperoxaluria type 36 tests
  • Primary hyperoxaluria, type I7 tests
  • Primary hyperoxaluria, type II7 tests
  • Progressive familial intrahepatic cholestasis type 24 tests
  • Propionic acidemia7 tests
  • Pseudo-Hurler polydystrophy7 tests
  • Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 12 tests
  • Pyknodysostosis7 tests
  • Pyruvate dehydrogenase E1-alpha deficiency3 tests
  • Pyruvate dehydrogenase E1-beta deficiency4 tests
  • Pyruvate dehydrogenase E3 deficiency9 tests
  • Recurrent pregnancy loss 41 test
  • Renal tubular acidosis with progressive nerve deafness6 tests
  • Retinal dystrophy4 tests
  • Retinitis pigmentosa 256 tests
  • Retinitis pigmentosa 266 tests
  • Retinitis pigmentosa 286 tests
  • Retinitis pigmentosa 599 tests
  • Rhizomelic chondrodysplasia punctata type 111 tests
  • Rhizomelic chondrodysplasia punctata type 34 tests
  • Roberts-SC phocomelia syndrome4 tests
  • Salla disease7 tests
  • Sandhoff disease7 tests
  • SchC6pf-Schulz-Passarge syndrome4 tests
  • Schimke immuno-osseous dysplasia4 tests
  • Severe autosomal recessive muscular dystrophy of childhood - North African type7 tests
  • Severe combined immunodeficiency due to DCLRE1C deficiency7 tests
  • Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency7 tests
  • Severe X-linked myotubular myopathy3 tests
  • Sj√∂gren-Larsson syndrome7 tests
  • SLC35A2-CDG2 tests
  • Smith-Lemli-Opitz syndrome16 tests
  • Solid tumor1 test
  • Sphingolipid activator protein 1 deficiency4 tests
  • Spinal muscular atrophy32 tests
  • Spondylocostal dysostosis 2, autosomal recessive4 tests
  • Spongy degeneration of central nervous system16 tests
  • Stuve-Wiedemann syndrome4 tests
  • Tay-Sachs disease27 tests
  • Triploidy1 test
  • Turner syndrome1 test
  • Twinning, monozygotic1 test
  • Tyrosinemia type I11 tests
  • Usher syndrome type 1B7 tests
  • Usher syndrome type 1C7 tests
  • Usher syndrome type 1D7 tests
  • Usher syndrome type 1F9 tests
  • Usher syndrome type 2A9 tests
  • Usher syndrome type 39 tests
  • Vanishing white matter disease7 tests
  • Very long chain acyl-CoA dehydrogenase deficiency7 tests
  • Wilson disease9 tests
  • Wolman disease6 tests
  • X-linked Alport syndrome3 tests
  • X-linked Emery-Dreifuss muscular dystrophy3 tests
  • X-linked severe combined immunodeficiency5 tests

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Genetic counseling, comments
  • Insurance appeals support
  • Insurance billing
  • SNP based array on POC: Order Code: Anora
  • Expanded Carrier Screening: Order Code: Horizon Carrier Screening, comments
  • Non-Invasive Prenatal Testing: Order Code: Panorama, comments
  • Preimplantation Genetic Diagnosis (PGD): Order Code: Spectrum, comments

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 05D1082992, Expiration date: 2022-05-13
  • CAP, Number: 8737934, Expiration date: 2022-02-20
  • ISO15189, Number: 13485:2003, Expiration date: 2022-03-17

Licenses

  • CA - California Department of Public Health CDPH, Number: CDF00337104, Expiration date: 2022-04-17
  • MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 1901, Effective date: 2018-07-01 Non-expiring
  • NY - New York State Department of Health NYSDOH, Number: 8417, Expiration date: 2022-06-30
  • PA - Pennsylvania Department of Health PADOH, Number: 32473, Expiration date: 2022-08-15
  • RI - State of Rhode Island Department of Health RIDOH, Number: LCO00978, Expiration date: 2022-12-31

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.