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Aventus Biolabs

GTR Lab ID: 507307, Last updated:2021-12-15
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Personnel

Conditions and tests

  • Abnormality of coagulation1 test
  • Actn3 deficiency1 test
  • Acute myeloid leukemia1 test
  • Adrenocortical carcinoma, hereditary1 test
  • Age related macular degeneration 12 tests
  • Alzheimer disease2 tests
  • Alzheimer disease 22 tests
  • Alzheimer disease 42 tests
  • Anterior segment dysgenesis 61 test
  • Anxiety2 tests
  • Apolipoprotein c-III deficiency1 test
  • Aryl hydrocarbon hydroxylase inducibility3 tests
  • Ataxia - telangiectasia variant1 test
  • Ataxia-telangiectasia-like disorder1 test
  • Atorvastatin response1 test
  • Bannayan-Riley-Ruvalcaba syndrome1 test
  • Barrett esophagus1 test
  • Bloom syndrome2 tests
  • Body mass index quantitative trait locus 142 tests
  • BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 201 test
  • Bone osteosarcoma2 tests
  • Breast neoplasm2 tests
  • Brugada syndrome1 test
  • Budd-Chiari syndrome2 tests
  • Capillary infantile hemangioma1 test
  • Cardiac-urogenital syndrome1 test
  • Carney complex - trismus - pseudocamptodactyly syndrome1 test
  • Carotid intimal medial thickness 12 tests
  • Cerebral arteriovenous malformation2 tests
  • Citalopram response1 test
  • Classic homocystinuria1 test
  • Clopidogrel response2 tests
  • Colorectal cancer1 test
  • Congenital prothrombin deficiency7 tests
  • Cowden syndrome 11 test
  • CYP2C19-related poor drug metabolism6 tests
  • Debrisoquine, poor metabolism of2 tests
  • Debrisoquine, ultrarapid metabolism of2 tests
  • Deficiency of steroid 17-alpha-monooxygenase1 test
  • Desmoid disease, hereditary1 test
  • Diabetes mellitus type 12 tests
  • Disorder due cytochrome p450 CYP2C19 variant3 tests
  • Disorder due cytochrome p450 CYP2C9 variant5 tests
  • Disorder due cytochrome p450 CYP2D6 variant6 tests
  • Disorder due cytochrome p450 CYP3A45 tests
  • Disorder due cytochrome p450 CYP3A5 variant3 tests
  • DNA ligase IV deficiency1 test
  • Dopamine receptor d2, reduced brain density of1 test
  • Dyskeratosis congenita1 test
  • Efavirenz response1 test
  • Ehlers-Danlos syndrome, arthrochalasis type2 tests
  • Ehlers-Danlos syndrome, classic type1 test
  • Ehlers-Danlos syndrome, classic type, 21 test
  • Encephalitis/encephalopathy, mild, with reversible myelin vacuolization1 test
  • Entacapone response1 test
  • Esomeprazole response1 test
  • Essential hypertension2 tests
  • Factor V deficiency4 tests
  • Familial colorectal cancer1 test
  • Familial cylindromatosis1 test
  • Familial melanoma2 tests
  • Familial multiple polyposis syndrome1 test
  • Familial multiple trichoepitheliomata1 test
  • Familial pancreatic carcinoma2 tests
  • Familial porphyria cutanea tarda1 test
  • Familial prostate carcinoma1 test
  • Familial type 3 hyperlipoproteinemia2 tests
  • Familial type 5 hyperlipoproteinemia1 test
  • Fanconi anemia complementation group C1 test
  • Fanconi-Bickel syndrome2 tests
  • Gastrointestinal stromal tumor1 test
  • Generalized juvenile polyposis/juvenile polyposis coli1 test
  • Glaucoma 3, primary infantile, B1 test
  • Glaucoma 3A1 test
  • GSTM1-related lung cancer2 tests
  • Hemochromatosis type 11 test
  • Hereditary breast ovarian cancer syndrome2 tests
  • Hereditary diffuse gastric adenocarcinoma1 test
  • Hereditary disease5 tests
  • Hereditary palmoplantar keratoderma1 test
  • Hereditary Paraganglioma-Pheochromacytoma Syndrome1 test
  • Hereditary pheochromocytoma-paraganglioma1 test
  • Homocystinuria due to methylene tetrahydrofolate reductase deficiency10 tests
  • Homocystinuria due to MTHFR deficiency1 test
  • Hyperalphalipoproteinemia 11 test
  • Hyperapobetalipoproteinemia, susceptibility to1 test
  • Hypercholesterolemia, familial, 11 test
  • Hyperlipidemia, familial combined, LPL related1 test
  • Hyperlipoproteinemia2 tests
  • Hyperlipoproteinemia, type I1 test
  • Hyperparathyroidism 2 with jaw tumors1 test
  • Hypertriglyceridemia, familial1 test
  • Hypothyroidism1 test
  • Infantile cortical hyperostosis2 tests
  • Inflammatory bowel disease 12 tests
  • Inherited susceptibility to asthma3 tests
  • Interleukin 6, serum level of, quantitative trait locus1 test
  • Intracerebral hemorrhage2 tests
  • Ischemic stroke5 tests
  • Kaposi sarcoma2 tests
  • Lethal polymalformative syndrome, Boissel type2 tests
  • Leukemia, acute myeloid, susceptibility to1 test
  • Li-Fraumeni syndrome1 test
  • Lipoprotein glomerulopathy2 tests
  • Lynch syndrome1 test
  • Major affective disorder 12 tests
  • Major depressive disorder2 tests
  • Major depressive disorder 12 tests
  • Major depressive disorder 22 tests
  • Malaria, susceptibility to3 tests
  • Medulloblastoma1 test
  • Melanoma, uveal, susceptibility to, 11 test
  • Melanoma, uveal, susceptibility to, 21 test
  • Methylcobalamin deficiency type cblE1 test
  • Methylcobalamin deficiency type cblG1 test
  • Microcephaly, normal intelligence and immunodeficiency1 test
  • Microvascular complications of diabetes, susceptibility to, 11 test
  • Microvascular complications of diabetes, susceptibility to, 32 tests
  • Microvascular complications of diabetes, susceptibility to, 63 tests
  • Microvascular complications of diabetes, susceptibility to, 71 test
  • Migraine3 tests
  • Mosaic variegated aneuploidy syndrome1 test
  • Muir-TorrĂ© syndrome1 test
  • Multiple congenital exostosis1 test
  • Multiple endocrine neoplasia2 tests
  • Multiple fibrofolliculomas1 test
  • Neoplasm2 tests
  • Neoplasm of stomach1 test
  • Neural tube defects, folate-sensitive4 tests
  • Neuroblastoma1 test
  • Neurofibromatosis, familial spinal1 test
  • Neurofibromatosis, type 11 test
  • Nicotine dependence1 test
  • Nijmegen breakage syndrome-like disorder1 test
  • Nonpersistence of intestinal lactase1 test
  • Obesity3 tests
  • Oligodontia-cancer predisposition syndrome1 test
  • Omeprazole response1 test
  • Opioid dependence, susceptibility to, 11 test
  • Osteoarthritis, hip1 test
  • Osteogenesis imperfecta type I2 tests
  • Osteogenesis imperfecta type III2 tests
  • Osteogenesis imperfecta with normal sclerae, dominant form2 tests
  • Osteogenesis imperfecta, recessive perinatal lethal2 tests
  • Palmoplantar keratoderma-esophageal carcinoma syndrome1 test
  • Panic disorder 13 tests
  • Peutz-Jeghers syndrome1 test
  • Pleuropulmonary blastoma1 test
  • PLIN1-related familial partial lipodystrophy1 test
  • Postmenopausal osteoporosis2 tests
  • Preeclampsia2 tests
  • Pregnancy loss, recurrent, susceptibility to, 12 tests
  • Pregnancy loss, recurrent, susceptibility to, 21 test
  • Primary familial hypertrophic cardiomyopathy1 test
  • Primary pigmented nodular adrenocortical disease1 test
  • Proteus syndrome1 test
  • Renal tubular dysgenesis2 tests
  • Retinitis pigmentosa1 test
  • Retinoblastoma1 test
  • Rhabdoid tumor predisposition syndrome 11 test
  • Rothmund-Thomson syndrome2 tests
  • Rotor syndrome1 test
  • Schizophrenia6 tests
  • Schwannomatosis1 test
  • Sea-blue histiocyte syndrome2 tests
  • Seckel syndrome 11 test
  • Selective serotonin reuptake inhibitor response2 tests
  • Shwachman-Diamond syndrome 11 test
  • Simpson-Golabi-Behmel syndrome type 11 test
  • Simvastatin response1 test
  • Soluble interleukin-6 receptor, serum level of, quantitative trait locus1 test
  • Squamous cell carcinoma1 test
  • Statin causing adverse effect in therapeutic use3 tests
  • Statin-induced myopathy1 test
  • Systemic-onset juvenile idiopathic arthritis2 tests
  • Thrombophilia due to activated protein C resistance6 tests
  • Thrombophilia due to thrombin defect7 tests
  • Thyroid gland carcinoma1 test
  • Transferrin serum level quantitative trait locus 21 test
  • Tuberous sclerosis syndrome2 tests
  • Type 2 diabetes mellitus2 tests
  • Variegate porphyria1 test
  • Venous thrombosis, susceptibility to1 test
  • Vitamin D-dependent rickets type II with alopecia2 tests
  • Vitamin K-dependent clotting factors, combined deficiency of, type 12 tests
  • Vitamin K-dependent clotting factors, combined deficiency of, type 21 test
  • Von Hippel-Lindau syndrome1 test
  • Warfarin response4 tests
  • Werner syndrome2 tests
  • Xeroderma pigmentosum1 test

List of services

  • Custom Deletion/Duplication Testing
  • Prenatal testing
  • Custom Sequence Analysis
  • Custom microarray analysis
  • Carrier testing
  • Data Storage and Backup
  • Genetic counseling
  • Insurance appeals support
  • Insurance billing
  • Insurance preauthorization
  • Insurance preverification
  • Preimplantation Genetic Diagnosis (PGD)
  • Result interpretation
  • Whole Exome Sequencing
  • Whole Genome Sequencing

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 10D2119613, Expiration date: 2023-02-28
  • CAP, Number: 9487683, Expiration date: 2023-03-27
  • COLA, Number: 26959, Expiration date: 2022-01-15

Licenses

  • FL - Florida Agency for Health Care Administration AHCA, Number: 26986106, Expiration date: 2030-01-30

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.