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6,967 Results - per page

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Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Record Last Update Mentions Count
DD0592
 
Resource Report
Resource Website
ECACC Cat# 92011716, RRID:CVCL_9A94 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92011716 ECACC:92011716,
Wikidata:Q54829140
CVCL_9A94 2026-07-25 04:29:32 0
DD0558
 
Resource Report
Resource Website
ECACC Cat# 91122404, RRID:CVCL_9A79 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91122404 ECACC:91122404,
Wikidata:Q54829119
CVCL_9A79 2026-07-25 04:29:32 0
DD0556
 
Resource Report
Resource Website
ECACC Cat# 91122402, RRID:CVCL_9A77 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91122402 ECACC:91122402,
Wikidata:Q54829117
CVCL_9A77 2026-07-25 04:29:32 0
DD0560
 
Resource Report
Resource Website
ECACC Cat# 91122407, RRID:CVCL_9A81 Homo sapiens (Human) Fragile X syndrome Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 91122407 ECACC:91122407,
Wikidata:Q54829121
CVCL_9A81 2026-07-25 04:29:34 0
DD0546
 
Resource Report
Resource Website
ECACC Cat# 91121825, RRID:CVCL_9A69 Homo sapiens (Human) Karyotypic information: 46,XY,inv(2)(p11;q13)(?0) (ECACC=91121825)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91121825 ECACC:91121825,
Wikidata:Q54829108
CVCL_9A69 2026-07-25 04:29:31 0
DD0554
 
Resource Report
Resource Website
ECACC Cat# 91122012, RRID:CVCL_AQ58 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91122012 ECACC:91122012,
Wikidata:Q54829115
CVCL_AQ58 2026-07-25 04:29:34 0
DD0647
 
Resource Report
Resource Website
ECACC Cat# 92022804, RRID:CVCL_9B18 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92022804 ECACC:92022804,
Wikidata:Q54829165
CVCL_9B18 2026-07-25 04:29:33 0
DD0684
 
Resource Report
Resource Website
ECACC Cat# 92033002, RRID:CVCL_9B42 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92033002 ECACC:92033002,
Wikidata:Q54829198
CVCL_9B42 2026-07-25 04:29:34 0
DD0644
 
Resource Report
Resource Website
ECACC Cat# 92022530, RRID:CVCL_9B15 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022530 ECACC:92022530,
Wikidata:Q54829162
CVCL_9B15 2026-07-25 04:29:33 0
DD0679
 
Resource Report
Resource Website
ECACC Cat# 92031910, RRID:CVCL_9B39 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92031910 ECACC:92031910,
Wikidata:Q54829195
CVCL_9B39 2026-07-25 04:29:34 0
DD0676
 
Resource Report
Resource Website
ECACC Cat# 92031713, RRID:CVCL_9B37 Homo sapiens (Human) Karyotypic information: 46,XY; 46,X,+mar(Y) (ECACC=92031713)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92031713 ECACC:92031713,
Wikidata:Q54829193
CVCL_9B37 2026-07-25 04:29:33 0
DD0655
 
Resource Report
Resource Website
ECACC Cat# 92030301, RRID:CVCL_9B25 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92030301 ECACC:92030301,
Wikidata:Q54829173
CVCL_9B25 2026-07-25 04:29:33 0
DD0705
 
Resource Report
Resource Website
ECACC Cat# 92041418, RRID:CVCL_9B51 Homo sapiens (Human) Karyotypic information: 46,XY,del(20)(p11.21;p11.23); de novo (ECACC=92041418)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92041418 ECACC:92041418,
Wikidata:Q54829207
CVCL_9B51 2026-07-25 04:29:34 0
DD0646
 
Resource Report
Resource Website
ECACC Cat# 92022803, RRID:CVCL_9B17 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022803 ECACC:92022803,
Wikidata:Q54829164
CVCL_9B17 2026-07-25 04:29:35 0
DD0677
 
Resource Report
Resource Website
ECACC Cat# 92031805, RRID:CVCL_9B38 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18 (ECACC=92031805)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92031805 ECACC:92031805,
Wikidata:Q54829194
CVCL_9B38 2026-07-25 04:29:35 0
DD0635
 
Resource Report
Resource Website
ECACC Cat# 92021925, RRID:CVCL_9B11 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XX,+18 (ECACC=92021925)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92021925 ECACC:92021925,
Wikidata:Q54829158
CVCL_9B11 2026-07-25 04:29:35 0
DD0711
 
Resource Report
Resource Website
ECACC Cat# 92042109, RRID:CVCL_9B56 Homo sapiens (Human) Congenital hydrocephalus Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92042109 ECACC:92042109,
Wikidata:Q54829212
CVCL_9B56 2026-07-25 04:29:35 0
DD0650
 
Resource Report
Resource Website
ECACC Cat# 92022807, RRID:CVCL_9B21 Homo sapiens (Human) Wolf-Hirschhorn syndrome Karyotypic information: 46,XY,-4,+?der(4)(qter->p16;?) (ECACC=92022807)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022807 ECACC:92022807,
Wikidata:Q54829169
CVCL_9B21 2026-07-25 04:29:33 0
DD0632
 
Resource Report
Resource Website
ECACC Cat# 92021922, RRID:CVCL_9B09 Homo sapiens (Human) Karyotypic information: 46,XX,del(1)(pter->q43)(?0) (ECACC=92021922)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92021922 ECACC:92021922,
Wikidata:Q54829156
CVCL_9B09 2026-07-25 04:29:33 0
DD0670
 
Resource Report
Resource Website
ECACC Cat# 92030647, RRID:CVCL_9B32 Homo sapiens (Human) Hydrops fetalis Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92030647 ECACC:92030647,
Wikidata:Q54829180
CVCL_9B32 2026-07-25 04:29:35 0

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