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- 1q21.1_copy_number_variations abstract "1q21.1 copy number variations (CNVs) are rare aberrations of human chromosome 1.In a common situation a human cell has one pair of identical chromosomes on chromosome 1. With the 1q21.1 CNVs one chromosome of the pair is not complete because a part of the sequence of the chromosome is missing, or overcomplete, because some parts of the sequence are duplicated. The result is that one chromosome is of normal length and the other one is too long or too short.".
- 1q21.1_copy_number_variations thumbnail Chromosome_1_to_1q21.1.jpg?width=300.
- 1q21.1_copy_number_variations wikiPageID "36460224".
- 1q21.1_copy_number_variations wikiPageLength "5541".
- 1q21.1_copy_number_variations wikiPageOutDegree "54".
- 1q21.1_copy_number_variations wikiPageRevisionID "620743809".
- 1q21.1_copy_number_variations wikiPageWikiLink 1q21.1_deletion_syndrome.
- 1q21.1_copy_number_variations wikiPageWikiLink 1q21.1_duplication_syndrome.
- 1q21.1_copy_number_variations wikiPageWikiLink 1q21.1_proximal_deletions_and_duplications.
- 1q21.1_copy_number_variations wikiPageWikiLink ANKRD35.
- 1q21.1_copy_number_variations wikiPageWikiLink BCL9.
- 1q21.1_copy_number_variations wikiPageWikiLink Base_pair.
- 1q21.1_copy_number_variations wikiPageWikiLink CD160.
- 1q21.1_copy_number_variations wikiPageWikiLink CHD1L.
- 1q21.1_copy_number_variations wikiPageWikiLink Category:Autosomal_monosomies_and_deletions.
- 1q21.1_copy_number_variations wikiPageWikiLink Category:Congenital_disorders.
- 1q21.1_copy_number_variations wikiPageWikiLink Category:Developmental_biology.
- 1q21.1_copy_number_variations wikiPageWikiLink Category:Hematology.
- 1q21.1_copy_number_variations wikiPageWikiLink Category:Human_genetics.
- 1q21.1_copy_number_variations wikiPageWikiLink Category:Medical_genetics.
- 1q21.1_copy_number_variations wikiPageWikiLink Category:Syndromes.
- 1q21.1_copy_number_variations wikiPageWikiLink Chromosomal_inversion.
- 1q21.1_copy_number_variations wikiPageWikiLink Chromosomal_translocation.
- 1q21.1_copy_number_variations wikiPageWikiLink Chromosome_1_(human).
- 1q21.1_copy_number_variations wikiPageWikiLink Copy-number_variation.
- 1q21.1_copy_number_variations wikiPageWikiLink Deletion_(genetics).
- 1q21.1_copy_number_variations wikiPageWikiLink FMO5.
- 1q21.1_copy_number_variations wikiPageWikiLink GJA5.
- 1q21.1_copy_number_variations wikiPageWikiLink GJA8.
- 1q21.1_copy_number_variations wikiPageWikiLink GPR89A.
- 1q21.1_copy_number_variations wikiPageWikiLink GPR89B.
- 1q21.1_copy_number_variations wikiPageWikiLink GPR89C.
- 1q21.1_copy_number_variations wikiPageWikiLink Gene_duplication.
- 1q21.1_copy_number_variations wikiPageWikiLink HYDIN2.
- 1q21.1_copy_number_variations wikiPageWikiLink Hemojuvelin.
- 1q21.1_copy_number_variations wikiPageWikiLink ITGA10.
- 1q21.1_copy_number_variations wikiPageWikiLink LIX1L.
- 1q21.1_copy_number_variations wikiPageWikiLink Low_copy_repeats.
- 1q21.1_copy_number_variations wikiPageWikiLink Lysophosphatidic_acid_phosphatase_type_6.
- 1q21.1_copy_number_variations wikiPageWikiLink Meiosis.
- 1q21.1_copy_number_variations wikiPageWikiLink Myomegalin.
- 1q21.1_copy_number_variations wikiPageWikiLink NBPF10.
- 1q21.1_copy_number_variations wikiPageWikiLink NBPF11.
- 1q21.1_copy_number_variations wikiPageWikiLink NUDT17.
- 1q21.1_copy_number_variations wikiPageWikiLink Non-allelic_homologous_recombination.
- 1q21.1_copy_number_variations wikiPageWikiLink PDIA3P.
- 1q21.1_copy_number_variations wikiPageWikiLink PDZK1.
- 1q21.1_copy_number_variations wikiPageWikiLink PDZK1P1.
- 1q21.1_copy_number_variations wikiPageWikiLink PEX11B.
- 1q21.1_copy_number_variations wikiPageWikiLink PIAS3.
- 1q21.1_copy_number_variations wikiPageWikiLink POLR3C.
- 1q21.1_copy_number_variations wikiPageWikiLink POLR3GL.
- 1q21.1_copy_number_variations wikiPageWikiLink PRKAB2.
- 1q21.1_copy_number_variations wikiPageWikiLink Phenotype.
- 1q21.1_copy_number_variations wikiPageWikiLink RBM8A.
- 1q21.1_copy_number_variations wikiPageWikiLink TAR_syndrome.
- 1q21.1_copy_number_variations wikiPageWikiLink TXNIP.
- 1q21.1_copy_number_variations wikiPageWikiLink ZNF364.
- 1q21.1_copy_number_variations wikiPageWikiLink File:Chromosome_1_to_1q21.1.jpg.
- 1q21.1_copy_number_variations wikiPageWikiLinkText "1q21.1 copy number variations".
- 1q21.1_copy_number_variations wikiPageUsesTemplate Template:Reflist.
- 1q21.1_copy_number_variations subject Category:Autosomal_monosomies_and_deletions.
- 1q21.1_copy_number_variations subject Category:Congenital_disorders.
- 1q21.1_copy_number_variations subject Category:Developmental_biology.
- 1q21.1_copy_number_variations subject Category:Hematology.
- 1q21.1_copy_number_variations subject Category:Human_genetics.
- 1q21.1_copy_number_variations subject Category:Medical_genetics.
- 1q21.1_copy_number_variations subject Category:Syndromes.
- 1q21.1_copy_number_variations hypernym Aberrations.
- 1q21.1_copy_number_variations type Disorder.
- 1q21.1_copy_number_variations type Pediatric.
- 1q21.1_copy_number_variations type Specialty.
- 1q21.1_copy_number_variations type Syndrome.
- 1q21.1_copy_number_variations comment "1q21.1 copy number variations (CNVs) are rare aberrations of human chromosome 1.In a common situation a human cell has one pair of identical chromosomes on chromosome 1. With the 1q21.1 CNVs one chromosome of the pair is not complete because a part of the sequence of the chromosome is missing, or overcomplete, because some parts of the sequence are duplicated. The result is that one chromosome is of normal length and the other one is too long or too short.".
- 1q21.1_copy_number_variations label "1q21.1 copy number variations".
- 1q21.1_copy_number_variations sameAs Q2649996.
- 1q21.1_copy_number_variations sameAs 1q21.1-copynumbervariaties.
- 1q21.1_copy_number_variations sameAs m.0k9c85x.
- 1q21.1_copy_number_variations sameAs Q2649996.
- 1q21.1_copy_number_variations wasDerivedFrom 1q21.1_copy_number_variations?oldid=620743809.
- 1q21.1_copy_number_variations depiction Chromosome_1_to_1q21.1.jpg.
- 1q21.1_copy_number_variations isPrimaryTopicOf 1q21.1_copy_number_variations.