PubMed Nucleotide Protein Genome Structure PopSet Taxonomy OMIM
The OMIM Morbid Map presents the cytogenetic map location of disease genes described in OMIM. For a map organized by chromosome, see the OMIM Gene Map. For more refined maps of genes and DNA segments, use NCBI Entrez Map Viewer and the Genome Database.
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  • Enter gene symbol, chromosomal location, or disorder keyword to search for, e.g. "recessive", "CYP1","5", "1pter", or "Xq".
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DisorderSymbol(s)OMIMLocation
Chromosome 18 pericentric inversion (4)DUP18pDEL18q, DUP81qDEL18p609334 18q22
Chromosome 18p deletion syndrome (4)DEL18p, C18DELp146390 18p
Chromosome 18q deletion syndrome (4)DEL18q601808 18q
Chromosome 19q13.11 deletion syndrome (4)DEL19q13.11, C19DELq13.11613026 19q13.11
Chromosome 1p36 deletion syndrome (4)DEL1p36, C1DELp36607872 1p36
Chromosome 1q21.1 deletion syndrome (4)DEL1q21, C1DELq21612474 1q21.1
Chromosome 1q21.1 duplication syndrome (4)DUP1q21, C1DUPq21612475 1q21.1
Chromosome 1q42-q44 deletion syndrome (4)DEL1q42q44, C1DELq42q44612337 1q42-q44
Chromosome 22q11.2 deletion syndrome, distal (4)DEL22q11.2, C22DELq11.2611867 22q11.2
Chromosome 22q11.2 microduplication syndrome (4)DUP22q11.2608363 22q11.2
Chromosome 22q13.3 deletion syndrome, 606232 (3)SHANK3, PSAP2, PROSAP2, KIAA1650, DEL22q13.3606230 22q13.3
Chromosome 2p16.1-p15 deletion syndrome (4)DEL2p16.1-p15, C2DELp161-p15612513 2p16.1-p15
Chromosome 2q31.2 deletion syndrome (4)DEL2q31612345 2q31.2
Chromosome 2q32-q33 deletion syndrome (4)DEL2q32q33, C2DELq32q33612313 2q32-q33
Chromosome 3q29 microdeletion syndrome (4)DEL3q29, MICRODEL3q29609425 3q29
Chromosome 3q29 microduplication syndrome (4)DUP3q29, MICRODUP3q29611936 3q29
Chromosome 6pter-p24 deletion syndrome (4)DEL6pter, C6DELpter612582 6pter-p24
Chromosome 7q11.23 duplication syndrome (4)DUP7q11.23, C7DUPq11.23609757 7q11.23
Chromosome 9p deletion syndrome (4)DEL9p, C9DELp158170 9p
Chromosome 9q subtelomeric deletion syndrome, 610253 (3)EHMT1, EUHMTASE1, DEL9q34607001 9q34.3
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