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256,031 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
DD3374
 
Resource Report
Resource Website
RRID:CVCL_9P43 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:99031813,
Wikidata:Q54830717
CVCL_9P43 2026-07-25 04:30:13 0
DD3418
 
Resource Report
Resource Website
ECACC Cat# 99060326, RRID:CVCL_9P61 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 99060326 ECACC:99060326,
Wikidata:Q54830736
CVCL_9P61 2026-07-25 04:30:14 0
DD3410
 
Resource Report
Resource Website
ECACC Cat# 99052013, RRID:CVCL_9P58 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99052013 ECACC:99052013,
Wikidata:Q54830733
CVCL_9P58 2026-07-25 04:30:14 0
DD3406
 
Resource Report
Resource Website
ECACC Cat# 99051301, RRID:CVCL_9P56 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 99051301 ECACC:99051301,
Wikidata:Q54830731
CVCL_9P56 2026-07-25 04:30:14 0
DD3390
 
Resource Report
Resource Website
RRID:CVCL_9P54 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:99033111,
Wikidata:Q54830728
CVCL_9P54 2026-07-25 04:30:14 0
DD3358
 
Resource Report
Resource Website
ECACC Cat# 99021006, RRID:CVCL_9M99 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99021006 ECACC:99021006,
Wikidata:Q54830710
CVCL_9M99 2026-07-25 04:30:13 0
DD3455
 
Resource Report
Resource Website
ECACC Cat# 99081611, RRID:CVCL_9P69 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 99081611 ECACC:99081611,
Wikidata:Q54830751
CVCL_9P69 2026-07-25 04:30:15 0
DD3340
 
Resource Report
Resource Website
ECACC Cat# 98122306, RRID:CVCL_9M95 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 98122306 ECACC:98122306,
Wikidata:Q54830704
CVCL_9M95 2026-07-25 04:30:13 0
DD3522
 
Resource Report
Resource Website
ECACC Cat# 00031407, RRID:CVCL_9N18 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00031407 ECACC:00031407,
Wikidata:Q54830786
CVCL_9N18 2026-07-25 04:30:15 0
DD3471
 
Resource Report
Resource Website
ECACC Cat# 99102831, RRID:CVCL_9N10 Homo sapiens (Human) Karyotypic information: 46,XY,inv(4)(q15.32;q13.2)pat (ECACC=99102831)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 99102831 ECACC:99102831,
Wikidata:Q54830758
CVCL_9N10 2026-07-25 04:30:15 0
DD3499
 
Resource Report
Resource Website
RRID:CVCL_9P79 Homo sapiens (Human) Karyotypic information: 47,XX,+mar (ECACC=00013124)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:00013124,
Wikidata:Q54830767
CVCL_9P79 2026-07-25 04:30:15 0
DD3528
 
Resource Report
Resource Website
ECACC Cat# 00032003, RRID:CVCL_9P91 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 00032003 ECACC:00032003,
Wikidata:Q54830787
CVCL_9P91 2026-07-25 04:30:15 0
DD3544
 
Resource Report
Resource Website
RRID:CVCL_9N26 Homo sapiens (Human) Karyotypic information: 46,XY,t(7;18)(q11.2;q23) (ECACC=00050802)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:00050802,
Wikidata:Q54830797
CVCL_9N26 2026-07-25 04:30:16 0
DD3471
 
Resource Report
Resource Website
RRID:CVCL_9N10 Homo sapiens (Human) Karyotypic information: 46,XY,inv(4)(q15.32;q13.2)pat (ECACC=99102831)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:99102831,
Wikidata:Q54830758
CVCL_9N10 2026-07-25 04:30:15 0
DD3550
 
Resource Report
Resource Website
ECACC Cat# 00060704, RRID:CVCL_9P95 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(qter->p22.31 or p22.32) (ECACC=00060704)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00060704 ECACC:00060704,
Wikidata:Q54830801
CVCL_9P95 2026-07-25 04:30:16 0
DD3512
 
Resource Report
Resource Website
RRID:CVCL_9N15 Homo sapiens (Human) Karyotypic information: 46,Y,add(X)(q28) (ECACC=00022418)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:00022418,
Wikidata:Q54830775
CVCL_9N15 2026-07-25 04:30:15 0
DD3531
 
Resource Report
Resource Website
ECACC Cat# 00041222, RRID:CVCL_9P92 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 00041222 ECACC:00041222,
Wikidata:Q54830788
CVCL_9P92 2026-07-25 04:30:16 0
DD3532
 
Resource Report
Resource Website
RRID:CVCL_9N19 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:00041223,
Wikidata:Q54830789
CVCL_9N19 2026-07-25 04:30:16 0
DD3470
 
Resource Report
Resource Website
RRID:CVCL_9P74 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:99102243,
Wikidata:Q54830757
CVCL_9P74 2026-07-25 04:30:15 0
DD3493
 
Resource Report
Resource Website
RRID:CVCL_9P78 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:00111020,
Wikidata:Q54830766
CVCL_9P78 2026-07-25 04:30:15 0

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