81298-2

LOINC Code


LOINC code81298-2
name
descriptionThe 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 [LOINC: 81287-5], 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.
statusTRIAL

Fully-Specified Name

componentStructural variant cytogenetic location
propertyID  =  Identifier
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
system^Patient
scaleNom  =  Nominal:  Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody.
method

Additional Names

short nameIdent; Identifier; Molecular pathology; MOLPATH; Nominal; Point in time; Random; Struct var; Struct var cyto loc

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationStruct var cyto

History/Usage

first released
last updated2.56
last change typeADD  - added

Related Names



Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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