Versiti Diagnostic Laboratories

Versiti Diagnostic Laboratories
Versiti, Inc (Versiti)
638 North 18th Street
Milwaukee, Wisconsin, United States 53233
Phone: 800-245-3117 ext 6250
Fax: 414-937-6290
Email: labinfo@versiti.org
Online Contact: https://www.versiti.org/medical-professionals/products-services/request-information
Website: https://www.versiti.org/medical-professionals/products-services/diagnostic-labs
Affiliated with:
- Versiti, https://www.versiti.org/

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GTR Lab ID: 320366, Last updated:2023-06-08

Personnel

Director: Matthew Anderson, PhD, MD, Medical Director
Phone: (414) 937-6419
Fax: (414) 937-6202
Email: MAnderson@Versiti.org
Director: Brian Curtis, PhD, MLS(ASCP), SBB(ASCP), Lab Director
Phone: (414) 937-6255
Fax: (414) 937-6245
Email: BRCurtis@versiti.org
Director: Kenneth Friedman, MD, ABIM, Medical Director
Phone: (414) 937-6494
Fax: (414) 933-6803
Email: KDFriedman@Versiti.org
Director: Sandra Haberichter, PhD, Lab Director
Phone: 414-937-6488
Fax: 414-937-6404
Email: SHaberichter@Versiti.org
Director: Jennifer Schiller, PhD, Lab Director
Phone: (414) 937-6053
Fax: (414) 937-6322
Email: JJSchiller@Versiti.org
Director: Valerie Trapp-Stamborski, PhD, Lab Director
Phone: 414-937-6363
Email: VStamborski@Versiti.org
Michael Janasik, MS, BS, MBA, Marketing Director
Phone: 414-937-6290
Fax: 414-937-6202
Email: mcjanasik@versiti.org
Stefanie Dugan, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
Phone: (414) 937-6126
Fax: (414) 937-6202
Email: SDugan@Versiti.org
Juliana Perez Botero, MD, Medical Director
Phone: 414-937-3848
Email: JPerezBotero@Versiti.org

Conditions and tests

180 conditions/phenotypes with 144 tests
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3-Methylglutaconic aciduria type 21 test
Acquired hypoprothrombinemia1 test
Acquired polycythemia vera4 tests
Acquired secondary polycythemia1 test
ACTB-associated syndromic thrombocytopenia4 tests
Acute myeloid leukemia6 tests
Afibrinogenemia1 test
Alpha-1-antitrypsin deficiency1 test
Alpha-2-plasmin inhibitor deficiency2 tests
ARPC1B-related thrombocytopenia4 tests
Arthrogryposis, renal dysfunction, and cholestasis 15 tests
Arthrogryposis, renal dysfunction, and cholestasis 25 tests
Atypical hemolytic-uremic syndrome1 test
Autosomal dominant nonsyndromic hearing loss 171 test
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency1 test
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency1 test
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency1 test
Bernard Soulier syndrome8 tests
Bernard-Soulier syndrome, type A11 test
Bernard-Soulier syndrome, type A1 (recessive)1 test
Bernard-Soulier syndrome, type A2, autosomal dominant2 tests
Bernard-Soulier syndrome, type B1 test
Beta-thalassemia-X-linked thrombocytopenia syndrome1 test
Bleeding diathesis due to thromboxane synthesis deficiency4 tests
Bleeding disorder, platelet-type, 216 tests
BLOOD GROUP, RH SYSTEM2 tests
BLOOD GROUP--KIDD SYSTEM1 test
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency1 test
Budd-Chiari syndrome1 test
Chronic myelogenous leukemia, BCR-ABL1 positive3 tests
Chédiak-Higashi syndrome4 tests
Cohen syndrome1 test
Congenital afibrinogenemia1 test
Congenital amegakaryocytic thrombocytopenia3 tests
Congenital neutropenia-myelofibrosis-nephromegaly syndrome1 test
Congenital plasminogen activator inhibitor type 1 deficiency3 tests
Congenital prothrombin deficiency2 tests
Cyclical neutropenia3 tests
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder3 tests
Deficiency of phospholipase A2, group IVA1 test
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome4 tests
Disorder of cardiovascular system1 test
Duffy Blood group system1 test
Dysfibrinogenemia1 test
Erythrokeratodermia variabilis et progressiva 44 tests
Essential thrombocythemia7 tests
Factor 5 and Factor VIII, combined deficiency of, 23 tests
Factor V and factor VIII, combined deficiency of, type 13 tests
Factor VII deficiency3 tests
Factor X deficiency3 tests
Factor XI deficiency1 test
Factor XIII, A subunit, deficiency of4 tests
Factor XIII, b subunit, deficiency of4 tests
Familial dysfibrinogenemia1 test
Familial hemophagocytic lymphohistiocytosis3 tests
Familial hypodysfibrinogenemia1 test
Familial visceral amyloidosis, Ostertag type1 test
Fibrinolytic defect1 test
FLNA-related thrombocytopenia4 tests
Ghosal hematodiaphyseal dysplasia3 tests
Giant platelet disorder, isolated1 test
Glanzmann thrombasthenia6 tests
GNE-related thrombocytopenia3 tests
Graft-versus-host disease, susceptibility to1 test
Gray platelet syndrome5 tests
Griscelli syndrome type 21 test
Hb SS disease4 tests
Hemoglobinopathy1 test
Hemolytic disease of fetus OR newborn due to isoimmunization1 test
Hemolytic uremic syndrome, atypical, susceptibility to, 11 test
Hemophilia1 test
Hemophilia A with vascular abnormality1 test
Hemophilia A, FVIII Deficiency1 test
Hemophilia B Brandenburg1 test
Hemophilia B leyden1 test
Hemophilia b(m)1 test
Hemophilia B, Factor IX Deficiency1 test
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation2 tests
Hereditary antithrombin deficiency1 test
Hereditary factor I deficiency disease1 test
Hereditary factor IX deficiency disease2 tests
Hereditary factor VIII deficiency disease4 tests
Hereditary factor XI deficiency disease3 tests
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX16 tests
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency1 test
Hermansky-Pudlak syndrome1 test
Hermansky-Pudlak syndrome 15 tests
Hermansky-Pudlak syndrome 104 tests
Hermansky-Pudlak syndrome 25 tests
Hermansky-Pudlak syndrome 35 tests
Hermansky-Pudlak syndrome 45 tests
Hermansky-Pudlak syndrome 55 tests
Hermansky-Pudlak syndrome 65 tests
Hermansky-Pudlak syndrome 75 tests
Hermansky-Pudlak syndrome 84 tests
Hermansky-Pudlak syndrome 94 tests
High molecular weight kininogen deficiency1 test
Hypodysfibrinogenemia1 test
Hypofibrinogenemia1 test
Kell blood group system1 test
Leukocyte adhesion deficiency 34 tests
Lymphoma1 test
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss1 test
Macrothrombocytopenia, isolated, 1, autosomal dominant4 tests
Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome4 tests
Malaria, susceptibility to2 tests
Mesangiocapillary glomerulonephritis, type II1 test
Mild hemophilia A1 test
Mild hemophilia B1 test
Moderately severe hemophilia A1 test
Moderately severe hemophilia B1 test
MPIG6B-related thrombocytopenia3 tests
Myelodysplastic syndrome2 tests
Myelofibrosis with myeloid metaplasia1 test
MYH9-related disorder3 tests
NBEA-related platelet dysfunction3 tests
Neutropenia, severe congenital, 1, autosomal dominant1 test
Neutrophil immunodeficiency syndrome1 test
Nonarteritic anterior ischemic optic neuropathy, susceptibility to1 test
Paris-Trousseau thrombocytopenia6 tests
Platelet-type bleeding disorder 113 tests
Platelet-type bleeding disorder 154 tests
Platelet-type bleeding disorder 163 tests
Platelet-type bleeding disorder 176 tests
Platelet-type bleeding disorder 184 tests
Platelet-type bleeding disorder 195 tests
Platelet-type bleeding disorder 205 tests
Platelet-type bleeding disorder 84 tests
Poikiloderma with neutropenia1 test
Posttransfusion purpura2 tests
Pregnancy loss, recurrent, susceptibility to, 11 test
Primary immunodeficiency syndrome due to p14 deficiency1 test
Primary myelofibrosis6 tests
Pseudo von Willebrand disease7 tests
Quebec platelet disorder2 tests
Radial aplasia-thrombocytopenia syndrome3 tests
Radioulnar synostosis with amegakaryocytic thrombocytopenia 14 tests
Radioulnar synostosis with amegakaryocytic thrombocytopenia 24 tests
Reduced coagulation factor V activity2 tests
Refractory anemia with ringed sideroblasts (clinical)1 test
Rh-null, regulator type2 tests
Roifman syndrome3 tests
SCOTT SYNDROME4 tests
Severe congenital neutropenia3 tests
Severe hemophilia A1 test
Severe hemophilia B1 test
Sitosterolemia with macrothrombocytopenia7 tests
Stormorken syndrome5 tests
Symptomatic form of hemophilia A in female carriers1 test
Symptomatic form of hemophilia B in female carriers1 test
THPO-related thrombocytopenia2 tests
Thrombocytopenia2 tests
Thrombocytopenia 11 test
Thrombocytopenia 24 tests
Thrombocytopenia 34 tests
Thrombocytopenia 44 tests
Thrombocytopenia 54 tests
Thrombocytopenia 65 tests
Thrombocytopenia, X-linked, intermittent1 test
Thrombocytopenia, X-linked, with or without dyserythropoietic anemia4 tests
Thrombophilia due to activated protein C resistance1 test
Thrombophilia, familial, due to decreased release of tissue plasminogen activator1 test
Thrombophilia, susceptibility to, due to factor V Leiden1 test
Thrombotic disease1 test
Transcription level of plasminogen activator inhibitor 11 test
Upshaw-Schulman syndrome1 test
Vitamin K-dependent clotting factors, combined deficiency of, type 12 tests
Vitamin K-dependent clotting factors, combined deficiency of, type 22 tests
von Willebrand disease type 11 test
von Willebrand disease type 23 tests
Von Willebrand disease type 2A1 test
Von Willebrand disease type 2B1 test
von Willebrand disease type 2M3 tests
von Willebrand disease type 2N3 tests
von Willebrand disease type 32 tests
von Willebrand disorder4 tests
Warts, hypogammaglobulinemia, infections, and myelokathexis1 test
Wiskott-Aldrich syndrome3 tests
Wiskott-Aldrich syndrome 23 tests
X-linked severe congenital neutropenia2 tests

List of services

Clinical Testing/Confirmation of Mutations Identified Previously
Confirmation of research findings
Custom Sequence Analysis
Genetic counseling
Maternal cell contamination study (MCC)
Mutation Confirmation
Custom Deletion/Duplication Testing: Order Code: 4800
Carrier testing: Order Code: 4970, comments
Testing is only available for genes tested by BloodCenter of Wisconsin. Please provide a copy of the affected relative's lab report for the variant being tested.

List of certifications/licenses

Certifications

CLIAHelpCertification number assigned by the Clinical Laboratory Improvement Amendments (CLIA) program to the laboratory director. Minimal field for US labs offering clinical tests. Optional field for international labs or US labs performing research tests. If pending renewal or record has not been updated, the expiration date may be in the past., Number: 52D1009037, Expiration date: 2025-01-30
AABB, Number: 006090, Expiration date: 2023-03-31
ASHI, Number: 11-4-WI-04-1, Expiration date: 2023-08-31
CAP, Number: 1780801, Expiration date: 2024-03-10

Licenses

CA - California Department of Public Health CDPH, Number: COS 800214, Expiration date: 2024-02-29
MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 954, Effective date: 2018-10-12 Non-expiring
NY - New York State Department of Health NYSDOH, Number: 4987, Expiration date: 2023-06-30
PA - Pennsylvania Department of Health PADOH, Number: 028864A, Expiration date: 2023-08-15

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.