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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
DD0588
 
Resource Report
Resource Website
ECACC Cat# 92011712, RRID:CVCL_9A90 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92011712 ECACC:92011712,
Wikidata:Q54829130
CVCL_9A90 2026-07-25 04:29:34 0
DD0576
 
Resource Report
Resource Website
ECACC Cat# 92011010, RRID:CVCL_9A87 Homo sapiens (Human) Trisomy 21 Karyotypic information: 47,XY,+21 (ECACC=92011010)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92011010 ECACC:92011010,
Wikidata:Q54829127
CVCL_9A87 2026-07-25 04:29:34 0
DD0617
 
Resource Report
Resource Website
ECACC Cat# 92020612, RRID:CVCL_9B02 Homo sapiens (Human) Karyotypic information: 46,XX; 47,XX+mar(5 or 19); de novo (ECACC=92020612)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92020612 ECACC:92020612,
Wikidata:Q54829148
CVCL_9B02 2026-07-25 04:29:34 0
DD0555
 
Resource Report
Resource Website
ECACC Cat# 91122401, RRID:CVCL_9A76 Homo sapiens (Human) Karyotypic information: 46,XY,del(22)(q11.21->q11.22) (ECACC=91122401)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91122401 ECACC:91122401,
Wikidata:Q54829116
CVCL_9A76 2026-07-25 04:29:32 0
DD0561
 
Resource Report
Resource Website
ECACC Cat# 91122406, RRID:CVCL_9A82 Homo sapiens (Human) Fragile X syndrome Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 91122406 ECACC:91122406,
Wikidata:Q54829122
CVCL_9A82 2026-07-25 04:29:32 0
DD0602
 
Resource Report
Resource Website
ECACC Cat# 92012819, RRID:CVCL_9A97 Homo sapiens (Human) Karyotypic information: 46,XY,inv(3)(q21;q25) (ECACC=92012819)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92012819 ECACC:92012819,
Wikidata:Q54829143
CVCL_9A97 2026-07-25 04:29:32 0
DD0623
 
Resource Report
Resource Website
ECACC Cat# 92021321, RRID:CVCL_9B04 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92021321 ECACC:92021321,
Wikidata:Q54829151
CVCL_9B04 2026-07-25 04:29:32 0
DD0549
 
Resource Report
Resource Website
ECACC Cat# 91121908, RRID:CVCL_9A72 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91121908 ECACC:91121908,
Wikidata:Q54829111
CVCL_9A72 2026-07-25 04:29:31 0
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

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