NxGen MDx, NxGen

General information

NxGen MDx, NxGen

Grand Rapids
United States
Organization ID: 507143


View this laboratory in GTR

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 35


GeneSubmissionsLast Updated
ABCC83Apr 6, 2021
ACADVL1Jul 27, 2020
ALDH3A21Jun 3, 2021
ALPL2Jul 23, 2021
ATM2May 4, 2021
C11orf652May 4, 2021
CBS1Jun 4, 2021
CFTR4May 4, 2021
GAA2Apr 1, 2021
GBA2Jul 23, 2021
GCDH2Jun 3, 2021
HBA11Jun 3, 2021
HGD3Jul 23, 2021
IDUA2Apr 20, 2021
KCNJ111Jun 3, 2021
LAMB31May 4, 2021
LOC1066279812Jul 23, 2021
LOC1068046131Jun 3, 2021
LOC1116744721May 4, 2021
LOC1116744751May 4, 2021
MAN2B11Jun 3, 2021
MLC11Jun 3, 2021
PAH1Jun 3, 2021
SLC26A42Apr 20, 2021
TH1Mar 31, 2021
TPO1May 4, 2021

Testing in GTR

Disease nameNumber of tests
3-Methylglutaconic aciduria type 32 tests
Abetalipoproteinaemia2 tests
Achromatopsia 32 tests
Agenesis of the corpus callosum with peripheral neuropathy2 tests
Alkaptonuria2 tests
Alpha-1-antitrypsin deficiency1 test
Alport syndrome, autosomal recessive2 tests
Anemia, nonspherocytic hemolytic, due to G6PD deficiency4 tests
Arthrogryposis, mental retardation, and seizures2 tests
Aspartylglucosaminuria2 tests
Ataxia-telangiectasia syndrome2 tests
Atelosteogenesis type II2 tests
Autosomal recessive DOPA responsive dystonia2 tests
Autosomal recessive limb-girdle muscular dystrophy type 2D2 tests
Autosomal recessive limb-girdle muscular dystrophy type 2E2 tests
Autosomal recessive polycystic kidney disease2 tests
Bardet-Biedl syndrome 12 tests
Bardet-Biedl syndrome 102 tests
Biotinidase deficiency2 tests
Bloom syndrome3 tests
Bordetella parapertussis infectious disease1 test
Breast cancer, susceptibility to2 tests
Breast-ovarian cancer, familial 11 test
Breast-ovarian cancer, familial 22 tests
Breast-ovarian cancer, familial 31 test
Breast-ovarian cancer, familial 41 test
COVID-194 tests
Canavan Disease, Familial Form1 test
Carcinoma of colon1 test
Carcinoma of pancreas1 test
Carnitine palmitoyltransferase 1A deficiency2 tests
Carnitine palmitoyltransferase II deficiency, infantile2 tests
Ceroid lipofuscinosis neuronal 22 tests
Charlevoix-Saguenay spastic ataxia2 tests
Choroideremia2 tests
Citrullinemia type I2 tests
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1 test
Classic homocystinuria2 tests
Cohen syndrome2 tests
Colorectal cancer 101 test
Colorectal cancer, susceptibility to, 121 test
Congenital amegakaryocytic thrombocytopenia2 tests
Congenital disorder of glycosylation, type Ia2 tests
Cutaneous malignant melanoma 21 test
Cutaneous malignant melanoma 31 test
Cystic fibrosis9 tests
Deafness, autosomal recessive 1A2 tests
Deafness, autosomal recessive 4, with enlarged vestibular aqueduct2 tests
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase2 tests
Deficiency of alpha-mannosidase2 tests
Deficiency of butyryl-CoA dehydrogenase2 tests
Deficiency of steroid 11-beta-monooxygenase1 test
Dihydropyrimidine dehydrogenase deficiency3 tests
Duchenne muscular dystrophy2 tests
Dyskeratosis congenita autosomal recessive 12 tests
Ehlers-Danlos syndrome dermatosparaxis type2 tests
Endometrial carcinoma1 test
Enterovirus infectious disease1 test
Factor V deficiency1 test
Familial Mediterranean fever2 tests
Familial adenomatous polyposis 11 test
Familial cancer of breast1 test
Familial colorectal cancer1 test
Familial dysautonomia7 tests
Familial hyperinsulinism1 test
Familial isolated deficiency of vitamin E2 tests
Fanconi anemia, complementation group C6 tests
Finnish congenital nephrotic syndrome2 tests
Fragile X syndrome9 tests
GRACILE syndrome2 tests
Galactosylceramide beta-galactosidase deficiency2 tests
Gaucher disease type I6 tests
Generalized juvenile polyposis/juvenile polyposis coli1 test
Glucose-6-phosphate transport defect2 tests
Glutaric aciduria, type 12 tests
Glycogen storage disease due to glucose-6-phosphatase deficiency type IA6 tests
Glycogen storage disease type III2 tests
Glycogen storage disease, type II2 tests
Glycogen storage disease, type V2 tests
Hb SS disease5 tests
Hereditary cancer-predisposing syndrome1 test
Hereditary factor XI deficiency disease2 tests
Hereditary fructosuria2 tests
Hereditary nonpolyposis colorectal cancer type 41 test
Hereditary nonpolyposis colorectal cancer type 51 test
Hereditary nonpolyposis colorectal cancer type 81 test
Hurler syndrome2 tests
Hyperinsulinemic hypoglycemia, familial, 15 tests
Idiopathic nephrotic syndrome2 tests
Infantile hypophosphatasia2 tests
Influenza3 tests
Isovaleryl-CoA dehydrogenase deficiency2 tests
Joubert syndrome1 test
Joubert syndrome 25 tests
Junctional epidermolysis bullosa gravis of Herlitz2 tests
Junctional epidermolysis bullosa, non-Herlitz type2 tests
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome1 test
Juvenile retinoschisis2 tests
Kugelberg-Welander disease6 tests
Legionnaire disease, susceptibility to1 test
Li-Fraumeni syndrome 11 test
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency2 tests
Lynch syndrome I1 test
MPI-CDG2 tests
MYH-associated polyposis1 test
Malignant tumor of prostate1 test
Maple syrup urine disease5 tests
Maple syrup urine disease type 1A1 test
Maple syrup urine disease type 1B1 test
Maple syrup urine disease, type 35 tests
Medium-chain acyl-coenzyme A dehydrogenase deficiency2 tests
Megalencephalic leukoencephalopathy with subcortical cysts 12 tests
Metachromatic leukodystrophy2 tests
Metaphyseal chondrodysplasia, McKusick type2 tests
Microcephaly, normal intelligence and immunodeficiency2 tests
Mucolipidosis type IV6 tests
Muir-Torré syndrome1 test
Multiple sulfatase deficiency2 tests
Muscle eye brain disease2 tests
Mycoplasma pneumoniae pneumonia1 test
Nemaline myopathy1 test
Nemaline myopathy 25 tests
Nephropathic cystinosis2 tests
Neu-Laxova syndrome 12 tests
Neuronal ceroid lipofuscinosis 12 tests
Neuronal ceroid lipofuscinosis 32 tests
Neuronal ceroid lipofuscinosis 52 tests
Neuronal ceroid lipofuscinosis 82 tests
Niemann-Pick disease type C12 tests
Niemann-Pick disease, type A6 tests
Pancreatic cancer 21 test
Pancreatic cancer 31 test
Pancreatic cancer 41 test
Parainfluenza infectious disease1 test
Pendred syndrome2 tests
Peroxisome biogenesis disorder 1A (Zellweger)2 tests
Perrault syndrome 12 tests
Pertussis1 test
Peutz-Jeghers syndrome1 test
Phenylketonuria2 tests
Pituitary hormone deficiency, combined 22 tests
Polyglandular autoimmune syndrome, type 12 tests
Primary hyperoxaluria, type I2 tests
Primary hyperoxaluria, type II2 tests
Prothrombin deficiency, congenital4 tests
Pyknodysostosis2 tests
Renal carnitine transport defect2 tests
Retinitis pigmentosa 592 tests
Rhabdoid tumor predisposition syndrome 21 test
Rhizomelic chondrodysplasia punctata type 12 tests
Sialic acid storage disease, severe infantile type2 tests
Sialuria2 tests
Sjögren-Larsson syndrome2 tests
Smith-Lemli-Opitz syndrome2 tests
Spinal muscular atrophy5 tests
Spinal muscular atrophy, type II4 tests
Spongy degeneration of central nervous system6 tests
Tay-Sachs disease7 tests
Thrombophilia due to factor V Leiden2 tests
Turcot syndrome1 test
Tyrosinemia type I2 tests
Usher Syndrome, Type III6 tests
Usher syndrome type 1F6 tests
Varicella zoster infection1 test
Very long chain acyl-CoA dehydrogenase deficiency2 tests
Walker-Warburg Syndrome, Fktn-Related1 test
Werdnig-Hoffmann disease5 tests
Wilson disease2 tests
alpha Thalassemia4 tests
beta Thalassemia4 tests
respiratory syncytial virus infection2 tests
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