<?xml version="1.0" encoding="UTF-8"?><CodeSystem xmlns="http://hl7.org/fhir"><id value="genomicstudy-changetype"/><meta><lastUpdated value="2023-03-25T23:21:02.749-05:00"/><profile value="http://hl7.org/fhir/StructureDefinition/shareablecodesystem"/></meta><text><status value="generated"/><div xmlns="http://www.w3.org/1999/xhtml"><p>This code system <code>http://hl7.org/fhir/genomicstudy-changetype</code> defines the following codes:</p><table class="codes"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td style="white-space:nowrap">DNA<a name="genomicstudy-changetype-DNA"> </a></td><td>DNA change</td><td>Change that involves Deoxyribonucleic acid (DNA) sequences.</td></tr><tr><td style="white-space:nowrap">RNA<a name="genomicstudy-changetype-RNA"> </a></td><td>RNA change</td><td>Change that involves Ribonucleic Acid (RNA) sequences.</td></tr><tr><td style="white-space:nowrap">AA<a name="genomicstudy-changetype-AA"> </a></td><td>Protein/amino Acids change </td><td>Change that involves Amino Acid (AA) or protein sequences.</td></tr><tr><td style="white-space:nowrap">CHR<a name="genomicstudy-changetype-CHR"> </a></td><td>Chromosomal changes</td><td>Change that involves number or strcture of chromosomes.</td></tr><tr><td style="white-space:nowrap">CNV<a name="genomicstudy-changetype-CNV"> </a></td><td>Copy number variations</td><td>Change that involves copy number variations among various genomes.</td></tr></table></div></text><extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-wg"><valueCode value="cg"/></extension><extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status"><valueCode value="trial-use"/></extension><extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm"><valueInteger value="1"/></extension><url value="http://hl7.org/fhir/genomicstudy-changetype"/><identifier><system value="urn:ietf:rfc:3986"/><value value="urn:oid:2.16.840.1.113883.4.642.4.1977"/></identifier><version value="5.0.0"/><name value="GenomicStudyChangeType"/><title value="Genomic Study Change Type"/><status value="active"/><experimental value="true"/><date value="2022-08-17T15:48:24-05:00"/><publisher value="HL7 (FHIR Project)"/><contact><telecom><system value="url"/><value value="http://hl7.org/fhir"/></telecom><telecom><system value="email"/><value value="fhir@lists.hl7.org"/></telecom></contact><description value="The change type relevant to GenomicStudy analysis."/><jurisdiction><coding><system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/><code value="001"/><display value="World"/></coding></jurisdiction><caseSensitive value="true"/><valueSet value="http://hl7.org/fhir/ValueSet/genomicstudy-changetype"/><content value="complete"/><concept><code value="DNA"/><display value="DNA change"/><definition value="Change that involves Deoxyribonucleic acid (DNA) sequences."/></concept><concept><code value="RNA"/><display value="RNA change"/><definition value="Change that involves Ribonucleic Acid (RNA) sequences."/></concept><concept><code value="AA"/><display value="Protein/amino Acids change "/><definition value="Change that involves Amino Acid (AA) or protein sequences."/></concept><concept><code value="CHR"/><display value="Chromosomal changes"/><definition value="Change that involves number or strcture of chromosomes."/></concept><concept><code value="CNV"/><display value="Copy number variations"/><definition value="Change that involves copy number variations among various genomes."/></concept></CodeSystem>