Versiti Diagnostic Laboratories (Versiti, Inc)
General information
Versiti Diagnostic Laboratories
Versiti, Inc
638 North 18th Street
Milwaukee
Wisconsin
United States - 53233
https://www.versiti.org/medical-professionals/products-services/diagnostic-labs
Organization ID: 320366
Versiti, Inc
638 North 18th Street
Milwaukee
Wisconsin
United States - 53233
https://www.versiti.org/medical-professionals/products-services/diagnostic-labs
Organization ID: 320366
Personnel
- Stefanie Dugan, Genetic Counselor
Phone: 4149376126
Email: stefanie.dugan@bcw.edu - Mitchell Springer, Contact
Phone: 4149376438
Email: mspringer@versiti.org
Assertion criteria
Level: Assertion criteria provided
Summary of submissions to ClinVar
Total submissions: 10
Condition
Name | Submissions | Last Updated |
---|---|---|
Hereditary factor VIII deficiency disease | 1 | Mar 6, 2020 |
Von Willebrand disease type 2A | 3 | Mar 6, 2020 |
Von Willebrand disease type 2B | 3 | Mar 6, 2020 |
von Willebrand disease type 1 | 1 | Mar 6, 2020 |
von Willebrand disease type 2M | 3 | Mar 6, 2020 |
von Willebrand disease type 2N | 1 | Mar 6, 2020 |
Testing in GTR
Disease name | Number of tests |
---|---|
3-Methylglutaconic aciduria type 2 | 1 test |
ACTB-associated syndromic thrombocytopenia | 4 tests |
ARPC1B-related thrombocytopenia | 4 tests |
Acquired hypoprothrombinemia | 1 test |
Acquired polycythemia vera | 4 tests |
Acquired secondary polycythemia | 1 test |
Acute myeloid leukemia | 6 tests |
Afibrinogenemia | 1 test |
Alpha-1-antitrypsin deficiency | 1 test |
Alpha-2-plasmin inhibitor deficiency | 2 tests |
Arthrogryposis, renal dysfunction, and cholestasis 1 | 5 tests |
Arthrogryposis, renal dysfunction, and cholestasis 2 | 5 tests |
Atypical hemolytic-uremic syndrome | 1 test |
Autosomal dominant nonsyndromic hearing loss 17 | 1 test |
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency | 1 test |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | 1 test |
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency | 1 test |
BLOOD GROUP, RH SYSTEM | 2 tests |
BLOOD GROUP--KIDD SYSTEM | 1 test |
Bernard Soulier syndrome | 8 tests |
Bernard-Soulier syndrome, type A1 | 1 test |
Bernard-Soulier syndrome, type A1 (recessive) | 1 test |
Bernard-Soulier syndrome, type A2, autosomal dominant | 2 tests |
Bernard-Soulier syndrome, type B | 1 test |
Beta-thalassemia-X-linked thrombocytopenia syndrome | 1 test |
Bleeding disorder, platelet-type, 13, susceptibility to | 4 tests |
Bleeding disorder, platelet-type, 21 | 6 tests |
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency | 1 test |
Budd-Chiari syndrome | 1 test |
Chronic myelogenous leukemia, BCR-ABL1 positive | 3 tests |
Chédiak-Higashi syndrome | 4 tests |
Cohen syndrome | 1 test |
Congenital afibrinogenemia | 1 test |
Congenital amegakaryocytic thrombocytopenia | 3 tests |
Congenital neutropenia-myelofibrosis-nephromegaly syndrome | 1 test |
Congenital plasminogen activator inhibitor type 1 deficiency | 3 tests |
Congenital prothrombin deficiency | 2 tests |
Cyclical neutropenia | 3 tests |
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | 3 tests |
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome | 4 tests |
Deficiency of phospholipase A2, group IVA | 1 test |
Disorder of cardiovascular system | 1 test |
Duffy Blood group system | 1 test |
Dysfibrinogenemia | 1 test |
Erythrokeratodermia variabilis et progressiva 4 | 4 tests |
Essential thrombocythemia | 7 tests |
FLNA-related thrombocytopenia | 4 tests |
Factor 5 and Factor VIII, combined deficiency of, 2 | 3 tests |
Factor V and factor VIII, combined deficiency of, type 1 | 3 tests |
Factor V deficiency | 2 tests |
Factor VII deficiency | 3 tests |
Factor X deficiency | 3 tests |
Factor XI deficiency | 1 test |
Factor XIII, A subunit, deficiency of | 4 tests |
Factor XIII, b subunit, deficiency of | 4 tests |
Familial dysfibrinogenemia | 1 test |
Familial hemophagocytic lymphohistiocytosis | 3 tests |
Familial hypodysfibrinogenemia | 1 test |
Familial visceral amyloidosis, Ostertag type | 1 test |
Fibrinolytic defect | 1 test |
GNE-related thrombocytopenia | 3 tests |
Ghosal hematodiaphyseal dysplasia | 3 tests |
Giant platelet disorder, isolated | 1 test |
Glanzmann thrombasthenia | 6 tests |
Graft-versus-host disease, susceptibility to | 1 test |
Gray platelet syndrome | 5 tests |
Griscelli syndrome type 2 | 1 test |
Hb SS disease | 4 tests |
Hemoglobinopathy | 1 test |
Hemolytic disease of fetus OR newborn due to isoimmunization | 1 test |
Hemolytic uremic syndrome, atypical, susceptibility to, 1 | 1 test |
Hemophilia | 1 test |
Hemophilia A with vascular abnormality | 1 test |
Hemophilia A, FVIII Deficiency | 1 test |
Hemophilia B Brandenburg | 1 test |
Hemophilia B leyden | 1 test |
Hemophilia B, Factor IX Deficiency | 1 test |
Hemophilia b(m) | 1 test |
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation | 2 tests |
Hereditary antithrombin deficiency | 1 test |
Hereditary factor I deficiency disease | 1 test |
Hereditary factor IX deficiency disease | 2 tests |
Hereditary factor VIII deficiency disease | 4 tests |
Hereditary factor XI deficiency disease | 3 tests |
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | 6 tests |
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency | 1 test |
Hereditary von Willebrand disease | 4 tests |
Hermansky-Pudlak syndrome | 1 test |
Hermansky-Pudlak syndrome 1 | 5 tests |
Hermansky-Pudlak syndrome 10 | 4 tests |
Hermansky-Pudlak syndrome 2 | 5 tests |
Hermansky-Pudlak syndrome 3 | 5 tests |
Hermansky-Pudlak syndrome 4 | 5 tests |
Hermansky-Pudlak syndrome 5 | 5 tests |
Hermansky-Pudlak syndrome 6 | 5 tests |
Hermansky-Pudlak syndrome 7 | 5 tests |
Hermansky-Pudlak syndrome 8 | 4 tests |
Hermansky-Pudlak syndrome 9 | 4 tests |
High molecular weight kininogen deficiency | 1 test |
Hypodysfibrinogenemia | 1 test |
Hypofibrinogenemia | 1 test |
Kell blood group system | 1 test |
Leukocyte adhesion deficiency 3 | 4 tests |
Lymphoma | 1 test |
MPIG6B-related thrombocytopenia | 3 tests |
MYH9-related disorder | 3 tests |
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss | 1 test |
Macrothrombocytopenia, isolated, 1, autosomal dominant | 4 tests |
Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome | 4 tests |
Malaria, susceptibility to | 2 tests |
Mesangiocapillary glomerulonephritis, type II | 1 test |
Mild hemophilia A | 1 test |
Mild hemophilia B | 1 test |
Moderately severe hemophilia A | 1 test |
Moderately severe hemophilia B | 1 test |
Myelodysplastic syndrome | 2 tests |
Myelofibrosis with myeloid metaplasia | 1 test |
NBEA-related platelet dysfunction | 3 tests |
Neutropenia, severe congenital, 1, autosomal dominant | 1 test |
Neutrophil immunodeficiency syndrome | 1 test |
Nonarteritic anterior ischemic optic neuropathy, susceptibility to | 1 test |
Paris-Trousseau thrombocytopenia | 6 tests |
Platelet-type bleeding disorder 11 | 3 tests |
Platelet-type bleeding disorder 15 | 4 tests |
Platelet-type bleeding disorder 16 | 3 tests |
Platelet-type bleeding disorder 17 | 6 tests |
Platelet-type bleeding disorder 18 | 4 tests |
Platelet-type bleeding disorder 19 | 5 tests |
Platelet-type bleeding disorder 20 | 5 tests |
Platelet-type bleeding disorder 8 | 4 tests |
Poikiloderma with neutropenia | 1 test |
Posttransfusion purpura | 2 tests |
Pregnancy loss, recurrent, susceptibility to, 1 | 1 test |
Primary immunodeficiency syndrome due to p14 deficiency | 1 test |
Primary myelofibrosis | 6 tests |
Pseudo von Willebrand disease | 7 tests |
Quebec platelet disorder | 2 tests |
Radial aplasia-thrombocytopenia syndrome | 3 tests |
Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 | 4 tests |
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 | 4 tests |
Refractory anemia with ringed sideroblasts (clinical) | 1 test |
Rh-null, regulator type | 2 tests |
Roifman syndrome | 3 tests |
SCOTT SYNDROME | 4 tests |
Severe congenital neutropenia | 3 tests |
Severe hemophilia A | 1 test |
Severe hemophilia B | 1 test |
Sitosterolemia with macrothrombocytopenia | 7 tests |
Stormorken syndrome | 5 tests |
Symptomatic form of hemophilia A in female carriers | 1 test |
Symptomatic form of hemophilia B in female carriers | 1 test |
THPO-related thrombocytopenia | 2 tests |
Telangiectasia, hereditary hemorrhagic, type 2 | 1 test |
Thrombocytopenia | 2 tests |
Thrombocytopenia 1 | 1 test |
Thrombocytopenia 2 | 4 tests |
Thrombocytopenia 3 | 4 tests |
Thrombocytopenia 4 | 4 tests |
Thrombocytopenia 5 | 4 tests |
Thrombocytopenia 6 | 5 tests |
Thrombocytopenia, X-linked, intermittent | 1 test |
Thrombocytopenia, X-linked, with or without dyserythropoietic anemia | 4 tests |
Thrombophilia due to activated protein C resistance | 1 test |
Thrombophilia, familial, due to decreased release of tissue plasminogen activator | 1 test |
Thrombophilia, susceptibility to, due to factor V Leiden | 1 test |
Thrombotic disease | 1 test |
Transcription level of plasminogen activator inhibitor 1 | 1 test |
Upshaw-Schulman syndrome | 1 test |
Vitamin K-dependent clotting factors, combined deficiency of, type 1 | 2 tests |
Vitamin K-dependent clotting factors, combined deficiency of, type 2 | 2 tests |
Von Willebrand disease type 2A | 1 test |
Von Willebrand disease type 2B | 1 test |
Warts, hypogammaglobulinemia, infections, and myelokathexis | 1 test |
Wiskott-Aldrich syndrome | 3 tests |
Wiskott-Aldrich syndrome 2 | 3 tests |
X-linked severe congenital neutropenia | 2 tests |
von Willebrand disease type 1 | 1 test |
von Willebrand disease type 2 | 3 tests |
von Willebrand disease type 2M | 3 tests |
von Willebrand disease type 2N | 3 tests |
von Willebrand disease type 3 | 2 tests |