INVITAE CORP.
(NYSE: NVTA)

Invitae Corporation is a genetic information company. The Company is engaged in genetic diagnostics for hereditary disorders, including breast, colon and pancreatic cancer. The Company utilizes an integrated portfolio of laboratory processes, software tools and informatics capabilities to process deoxyribonucleic acid (DNA)-containing samples, analyze information about patient-specific genetic variation and generate test reports for physicians and their patients. The Company offers the following panels: Featured cancer panels, Featured cardiology panels and Featured neurology panels. The Company�s tools and services include genetic counseling services, to explain complex genetic concepts; Family History Tool, which allows digitally recording the patient�s pedigree, assessing their risks, as well as deciding on the appropriate genetic test, and Clinvitae, a database of clinically-observed genetic variants aggregated from public sources.

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Range - - -   (-%)
Open -
Previous Close 0.019
Bid Price 8.460
Bid Volume -
Ask Price 8.470
Ask Volume -
Volume -
Value -
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Delayed prices. Updated at 14 Feb 2024 13:00.
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About INVITAE CORP

Invitae Corporation is a genetic information company. The Company is engaged in genetic diagnostics for hereditary disorders, including breast, colon and pancreatic cancer. The Company utilizes an integrated portfolio of laboratory processes, software tools and informatics capabilities to process deoxyribonucleic acid (DNA)-containing samples, analyze information about patient-specific genetic variation and generate test reports for physicians and their patients. The Company offers the following panels: Featured cancer panels, Featured cardiology panels and Featured neurology panels. The Company�s tools and services include genetic counseling services, to explain complex genetic concepts; Family History Tool, which allows digitally recording the patient�s pedigree, assessing their risks, as well as deciding on the appropriate genetic test, and Clinvitae, a database of clinically-observed genetic variants aggregated from public sources.

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