Variantyx, Inc.

Personnel

Director: Christine Stanley, PhD, FACMG, Medical Director
Phone: +1 617-209-2090
Email: christine.stanley@variantyx.com
Shirel Weiss, PhD, Administrator
Phone: United States
Email: Shirel.weiss@variantyx.com
Allan Fisher, MD, ABMGG Board Certified, ABOG, FACMG, FACOG, Diplomate of the Amer, Medical Director
Phone: +1 617-209-2090
Email: allan.fisher@variantyx.com

Conditions and tests

97 conditions/phenotypes with 31 tests
Enter text to narrow down the list

Amyotrophic lateral sclerosis1 test
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia1 test
Ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability2 tests
Ataxia-telangiectasia syndrome1 test
Ataxia-telangiectasia-like disorder1 test
Autosomal recessive ataxia due to ubiquinone deficiency1 test
Autosomal recessive ataxia, Beauce type1 test
Autosomal recessive axonal neuropathy with neuromyotonia1 test
Autosomal recessive spinocerebellar ataxia 101 test
Autosomal recessive spinocerebellar ataxia 111 test
Autosomal recessive spinocerebellar ataxia 131 test
Autosomal recessive spinocerebellar ataxia 161 test
Autosomal recessive spinocerebellar ataxia 201 test
Azorean disease2 tests
Becker muscular dystrophy2 tests
Behavioral variant of frontotemporal dementia1 test
Charcot-Marie-Tooth disease1 test
Charlevoix-Saguenay spastic ataxia2 tests
Congenital myasthenic syndrome1 test
Congenital myopathy1 test
Dementia, frontotemporal, with or without parkinsonism1 test
Dementia, Lewy body, susceptibility to1 test
Dentatorubral-pallidoluysian atrophy2 tests
Developmental delay1 test
Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing1 test
Disorder of endocrine system1 test
Drug metabolism or response1 test
Duchenne muscular dystrophy2 tests
Dyssynergia2 tests
Dystonic disorder1 test
Epilepsy1 test
Episodic ataxia type 11 test
Episodic ataxia type 21 test
Episodic ataxia type 51 test
Episodic ataxia type 61 test
Fragile X syndrome2 tests
FRAXE1 test
Friedreich ataxia2 tests
Frontotemporal dementia2 tests
Frontotemporal dementia and/or amyotrophic lateral sclerosis2 tests
Genetic dementia1 test
Hereditary cancer1 test
Hereditary cancer-predisposing syndrome1 test
Hereditary disease13 tests
Hereditary liability to pressure palsies1 test
Hereditary motor and sensory neuropathy1 test
Hereditary spastic paraplegia1 test
Infantile onset spinocerebellar ataxia1 test
Intellectual developmental disorder with autism and dysmorphic facies1 test
Intellectual disability1 test
Intellectual disability-hypotonic facies syndrome, X-linked, 11 test
Kennedy disease1 test
Lewy body dementia1 test
Marinesco-Sjögren syndrome1 test
Miscarriage1 test
Mitochondrial disease2 tests
Movement disorder2 tests
Muscular dystrophy2 tests
Myotonic dystrophy type 21 test
Neuronopathy, distal hereditary motor1 test
Pontoneocerebellar hypoplasia1 test
Riboflavin transporter deficiency1 test
Solid tumor1 test
Spastic ataxia 41 test
Spastic ataxia 51 test
Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome1 test
Spinal muscular atrophy1 test
Spinocerebellar ataxia 431 test
Spinocerebellar ataxia 481 test
Spinocerebellar ataxia 72 tests
Spinocerebellar ataxia type 12 tests
Spinocerebellar ataxia type 102 tests
Spinocerebellar ataxia type 111 test
Spinocerebellar ataxia type 122 tests
Spinocerebellar ataxia type 131 test
Spinocerebellar ataxia type 141 test
Spinocerebellar ataxia type 172 tests
Spinocerebellar ataxia type 19/221 test
Spinocerebellar ataxia type 22 tests
Spinocerebellar ataxia type 211 test
Spinocerebellar ataxia type 231 test
Spinocerebellar ataxia type 261 test
Spinocerebellar ataxia type 271 test
Spinocerebellar ataxia type 281 test
Spinocerebellar ataxia type 291 test
Spinocerebellar ataxia type 341 test
Spinocerebellar ataxia type 351 test
Spinocerebellar ataxia type 362 tests
Spinocerebellar ataxia type 381 test
Spinocerebellar ataxia type 421 test
Spinocerebellar ataxia type 51 test
Spinocerebellar ataxia type 62 tests
Spinocerebellar ataxia type 82 tests
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy1 test
Steinert myotonic dystrophy syndrome1 test
Ultrasound anomalies1 test
Walker-Warburg congenital muscular dystrophy1 test

List of services

Whole Exome Sequencing
Whole Genome Sequencing

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: 22D2140582, Expiration date: 2024-11-13
CAP, Number: 8291875, Expiration date: 2024-08-31

Licenses

CA - California Department of Public Health CDPH, Number: CDS00800949, Expiration date: 2023-04-08
MA - Executive Office of Health and Human Services EOHHS, Number: 5438, Expiration date: 2024-02-12
MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 2894, Effective date: 2018-11-14 Non-expiring
PA - Pennsylvania Department of Health PADOH, Number: 36456, Expiration date: 2023-08-15
RI - State of Rhode Island Department of Health RIDOH, Number: LCO01241, Expiration date: 2024-12-30

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.