| dbo:description
| - одна из 23 пар человеческих хромосом (ru)
- avtosomni kromosom pri vrsti Homo sapiens (sl)
- chromosome humain (fr)
- cromosom dynol (cy)
- cromosoma autosómico humano (es)
- cromosoma humano (gl)
- cromosoma umano (it)
- human chromosome (en)
- humant kromosom (nn)
- ljudski hromosom (bs)
- মানব ক্রোমোজোম (bn)
- 사람의 염색체 (ko)
- Menschliches Chromosom (de)
- mänsklig kromosom 10 (sv)
- toplamda 22 çift olan otozomal insan kromozomlarından onuncusu (tr)
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| dbo:wikiPageExternalLink
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| dbo:wikiPageWikiLink
| - dbr:National_Center_for_Biotechnology_Information
- dbr:RET_proto-oncogene
- dbr:Transcription_factor
- dbr:Beare–Stevenson_cutis_gyrata_syndrome
- dbr:Consensus_CDS_Project
- dbr:Jackson–Weiss_syndrome
- dbr:C10orf67
- dbr:Proser2
- dbr:Human
- dbr:UCSC_Genome_Browser
- dbr:Nonsyndromic_deafness
- dbr:Cell_(biology)
- dbr:DNA
- dbr:Enzyme
- dbr:Protein
- dbr:Base_pair
- dbr:Parathyroid_gland
- dbr:Crouzon_syndrome
- dbr:Mitosis
- dbr:Pseudogene
- dbr:UniProt
- dbr:Usher_syndrome
- dbr:Tetrahydrobiopterin_deficiency
- dbr:Protocadherin
- dbr:Chromosome
- dbr:Autosome
- dbr:Porphyria
- dbr:Centromere
- dbr:Non-coding_RNA
- dbr:Cowden_syndrome
- dbr:Gene_prediction
- dbr:Ensembl_genome_database_project
- dbr:Genitopatellar_syndrome
- dbr:Barakat_syndrome
- dbr:Spondyloepimetaphyseal_dysplasia,_Pakistani_type
- dbr:Karyogram
- dbr:Multiple_endocrine_neoplasia_type_2
- dbc:Genes_on_human_chromosome_10
- dbr:Pfeiffer_syndrome
- dbr:Apert_syndrome
- dbr:Charcot–Marie–Tooth_disease
- dbr:Cockayne_syndrome
- dbr:Haploinsufficiency
- dbr:ARMH3
- dbr:FAM208b
- dbr:Fam188a
- dbr:PI4K2A
- dbr:XB130
- dbr:Long_non-coding_RNA
- dbr:CEFIP
- dbr:Transmembrane_protein_254
- dbr:Hermansky–Pudlak_syndrome
- dbr:G_banding
- dbr:HUGO_Gene_Nomenclature_Committee
- dbr:Leukemia,_acute_lymphocytic,_susceptibility_to,_1
- dbr:SCZD11
- dbc:Chromosomes_(human)
- dbr:ARID5B
- dbr:AS3MT
- dbr:AVPI1
- dbr:Ankyrin_repeat_domain_22
- dbr:CAMK1D
- dbr:CCAR1
- dbr:CCDC186
- dbr:CCDC3
- dbr:CCNY_(gene)
- dbr:CDC123
- dbr:CDH23
- dbr:COMMD3-BMI1
- dbr:CUTC_(gene)
- dbr:Carboxypeptidase_x,_m14_family_member_2
- dbr:Cerebral_dopamine_neurotrophic_factor
- dbr:DDX50
- dbr:DHX32
- dbr:DPYSL4
- dbr:Disco_interacting_protein_2_homolog_c
- dbr:Dnaj_(hsp40)_homolog,_subfamily_c,_member_9
- dbr:Dnaj_heat_shock_protein_family_(hsp40)_member_c12
- dbr:EBLN1
- dbr:ECD_(gene)
- dbr:EGR2
- dbr:EIF5AP1
- dbr:EPC1
- dbr:ERCC6
- dbr:F-box_and_leucine_rich_repeat_protein_15
- dbr:FAM107B
- dbr:FAM13C
- dbr:FAM170B_(gene)
- dbr:FAS-AS1
- dbr:FERM_and_PDZ_domain_containing_2
- dbr:FRA10AC1
- dbr:FRAT1
- dbr:FRAT2
- dbr:GATA3
- dbr:GHITM
- dbr:GPRIN2
- dbr:GTPBP4
- dbr:HELLS
- dbr:HKDC1
- dbr:KIN_(gene)
- dbr:MTG1
- dbr:NPM3
- dbr:NRBF2
- dbr:NSMCE4A
- dbr:OTUD1
- dbr:PAPSS2
- dbr:PCBD1
- dbr:PCDH15
- dbr:PIP4K2A
- dbr:PITRM1
- dbr:PLXDC2
- dbr:PRAP1
- dbr:Phospholysine_phosphohistidine_inorganic_pyrophosphate_phosphatase
- dbr:Pleckstrin_homology_domain_containing_S1
- dbr:Protein_DEPP
- dbr:Protein_FAM25
- dbr:RPP30
- dbr:RRP12
- dbr:RSU1
- dbr:RTKN2
- dbr:Redox-regulatory_protein_FAM213A
- dbr:Rho_gtpase_activating_protein_21
- dbr:SGPL1
- dbr:SPG9
- dbr:STAMBPL1
- dbr:STOX1
- dbr:SUPV3L1
- dbr:Serglycin
- dbr:Shootin_1
- dbr:Solute_carrier_family_16_member_12
- dbr:Synaptonemal_complex_central_element_protein_1
- dbr:TACC2
- dbr:TCTN3
- dbr:TMEM26
- dbr:TMEM72
- dbr:TYSND1
- dbr:UCN3
- dbr:USMG5
- dbr:USP6NL
- dbr:Ubiquitin_specific_peptidase_54
- dbr:WASHC2C
- dbr:WW_domain_binding_protein_1-like
- dbr:ZNF37A
- dbr:Zinc_finger_protein_438
- dbr:FGFR2
- dbr:Ensembl
- dbr:C10orf99
- dbr:Hirschprung_disease
- dbr:Protein-coding_genes
- dbr:UROS
- dbr:UTF1_(gene)
- dbr:Tbc1_domain_family,_member_12
- dbr:GRCh38
- dbr:TMEM10
- dbr:Glioblastoma_multiforme
- dbr:ALOX5
- dbr:PTEN_gene
- dbr:Congenital_erythropoietic_porphyria
- dbr:Genome_annotation
- dbr:Young-Simpson_syndrome
- dbr:ZRANB1
- dbr:Number_of_genes
- dbr:VIM-AS1
- dbr:Thiel–Behnke_corneal_dystrophy
- dbr:SDF-1_(biology)
- dbr:SMNDC1
- dbr:Wolman_syndrome
- dbr:Hypoparathyrodism,_deafness,_and_renal_dysplasia_syndrome
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| dbp:caption
| - One is from mother, one is from father. (en)
- in human male karyogram. (en)
- G-banding patterns of human chromosome 10 in three different resolutions . Band length in this diagram is based on the ideograms from ISCN . This type of ideogram represents actual relative band length observed under a microscope at the different moments during the mitotic process. (en)
- Chromosome 10 pair (en)
- Human chromosome 10 pair after G-banding. (en)
- G-banding ideogram of human chromosome 10 in resolution 850 bphs. Band length in this diagram is proportional to base-pair length. This type of ideogram is generally used in genome browsers . (en)
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| dbp:centromerePosition
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| dbp:chr
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| dbp:ensemblId
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| dbp:entrezId
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| dbp:genbankId
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| dbp:genes
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| dbp:header
| - G-banding ideograms of human chromosome 10 (en)
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| dbp:height
| - 1125 (xsd:integer)
- 2801 (xsd:integer)
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| dbp:image
| - Human chromosome 10 - 400 550 850 bphs.png (en)
- Human chromosome 10 ideogram vertical.svg (en)
- Human male karyotpe high resolution - Chromosome 10.png (en)
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| dbp:lengthBp
| - 134758134 (xsd:integer)
- (en)
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| dbp:ncbiId
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| dbp:refseqId
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| dbp:totalWidth
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| dbp:type
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| dbp:ucscId
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| dbp:width
| - 216 (xsd:integer)
- 1003 (xsd:integer)
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| dct:subject
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| rdfs:label
| - Chromosome 10 (en)
- Cromosoma 10 (ca)
- صبغي 10 (ar)
- Chromosom 10 (Mensch) (de)
- Cromosoma 10 (humano) (es)
- Cromosoma 10 (it)
- Chromosome 10 humain (fr)
- Chromosom 10 (pl)
- Cromossoma 10 (pt)
- Chromosoom 10 (nl)
- 10-я хромосома человека (ru)
- Хромосома 10 (людина) (uk)
- 10号染色体 (zh)
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