DeCS

Descriptor English:

Genomic Structural Variation

Descriptor Spanish:

Variación Estructural del Genoma

Spanish from Spain

Descriptor	variación estructural genómica
Entry term(s)	variación estructural del genoma
Scope note:	Diferencias contiguas a gran escala (1000-400.000 pares de bases) en el genoma del ADN entre individuos, debidas a la ELIMINACIÓN DE SECUENCIAS, la INSERCIÓN DE SECUENCIAS, o la INVERSIÓN DE SECUENCIAS.

Descriptor Portuguese:

Variação Estrutural do Genoma

Descriptor French:

Variation structurale du génome

Entry term(s):

Genome Structural Variant
Genome Structural Variants
Genome Structural Variation
Genome Structural Variations
Genomic Structural Variant
Genomic Structural Variants
Genomic Structural Variations
Structural Variant, Genome
Structural Variant, Genomic
Structural Variants, Genome
Structural Variants, Genomic
Structural Variation, Genome
Structural Variation, Genomic
Structural Variations, Genome
Structural Variations, Genomic
Variant, Genome Structural
Variant, Genomic Structural
Variants, Genome Structural
Variants, Genomic Structural
Variation, Genome Structural
Variation, Genomic Structural
Variations, Genome Structural
Variations, Genomic Structural

Tree number(s):

G05.365.795.297

RDF Unique Identifier:

https://id.nlm.nih.gov/mesh/D056914

Scope note:

Contiguous large-scale (1000-400,000 basepairs) differences in the genomic DNA between individuals, due to SEQUENCE DELETION; SEQUENCE INSERTION; or SEQUENCE INVERSION.

Allowable Qualifiers:

DE drug effects
GE genetics
IM immunology
PH physiology
RE radiation effects

Public MeSH Note:

2010

History Note:

2010

DeCS ID:

53761

Unique ID:

D056914

Documents indexed in the Virtual Health Library (VHL):

Click here to access the VHL documents

Date Established:

2010/01/01

Date of Entry:

2009/07/06

PHENOMENA AND PROCESSES

Genetic Phenomena [G05]

Genetic Phenomena

Genetic Variation [G05.365]

Genetic Variation

Polymorphism, Genetic [G05.365.795]

Polymorphism, Genetic

Genomic Structural Variation [G05.365.795.297]

Genomic Structural Variation

DNA Copy Number Variations [G05.365.795.297.500]

DNA Copy Number Variations

Pharmacogenomic Variants [G05.365.795.446]

Pharmacogenomic Variants

Polymorphism, Restriction Fragment Length [G05.365.795.595]

Polymorphism, Restriction Fragment Length

Polymorphism, Single Nucleotide [G05.365.795.598]

Polymorphism, Single Nucleotide

Polymorphism, Single-Stranded Conformational [G05.365.795.600]

Polymorphism, Single-Stranded Conformational

Genomic Structural Variation - Preferred

Concept UI	M0533370
Scope note	Contiguous large-scale (1000-400,000 basepairs) differences in the genomic DNA between individuals, due to SEQUENCE DELETION; SEQUENCE INSERTION; or SEQUENCE INVERSION.
Preferred term	Genomic Structural Variation
Entry term(s)	Genome Structural Variant Genome Structural Variants Genome Structural Variation Genome Structural Variations Genomic Structural Variant Genomic Structural Variants Genomic Structural Variations Structural Variant, Genome Structural Variant, Genomic Structural Variants, Genome Structural Variants, Genomic Structural Variation, Genome Structural Variation, Genomic Structural Variations, Genome Structural Variations, Genomic Variant, Genome Structural Variant, Genomic Structural Variants, Genome Structural Variants, Genomic Structural Variation, Genome Structural Variation, Genomic Structural Variations, Genome Structural Variations, Genomic Structural

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