HealthAssure
HealthAssureGood Life
LOINCObservation

LOINC Code 81298-2: Structural variant cytogenetic location Nom [ID]

81298-2 is a LOINC code used to identify Structural variant cytogenetic location Nom [ID] in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Structural variant cytogenetic location. It is commonly used with the system or sample type ^Patient.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Structural variant cytogenetic location. It is commonly used with the system or sample type ^Patient.

When is it used?

  • Used in lab systems, EHRs, and clinical data exchange.
  • May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
  • Status: TRIAL
  • Order vs observation: Observation

What it does not mean

  • The code identifies the observation or test, not the actual result.

Key facts

Structural variant cytogenetic location [Identifier]
Structural variant cytogenetic location
The chromosome region where the structural variant was found, for example, 17p12. This term may be used when more specific information, such as the structural variant reported start-end [LOINC81287-5], precision of boundaries [LOINC: 81288-3] and inner and outer start-end [LOINC: 81302-2] and [LOINC: 81301-4], respectively, cannot be or are not reported.
Ident; Identifier; Molecular pathology; MOLPATH; Nominal; Point in time; Random; Struct var; Struct var cyto loc

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

Structural variant cytogenetic location Nom [ID]Structural variant cytogenetic location [Identifier]Struct var cyto loc IDStructural variant cytogenetic locationMOLPATHIDPt

Frequently asked questions

Code details

Code81298-2
SystemLOINC
Display nameStructural variant cytogenetic location Nom [ID]
DescriptionStructural variant cytogenetic location
Short nameStruct var cyto loc ID
ComponentStructural variant cytogenetic location
PropertyID
TimingPt
System (specimen)^Patient
ScaleNom
ClassMOLPATH
StatusTRIAL
Order/ObservationObservation

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.56
Last changed2.56

Consumer names

Structural variant cytogenetic location

Part names

Structural variant cytogenetic locationIDPt^PatientNomIdentifierPoint in time (spot)

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.