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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
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 2026-08-15 04:27:06 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 2026-08-15 04:27:05 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 2026-08-15 04:27:05 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 2026-08-15 04:27:07 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 2026-08-15 04:27:05 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 2026-08-15 04:27:07 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 2026-08-15 04:27:07 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 2026-08-15 04:27:05 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 2026-08-15 04:27:05 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 2026-08-15 04:27:06 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 2026-08-15 04:27:06 0
DD3503
 
Resource Report
Resource Website
ECACC Cat# 00021515, RRID:CVCL_9P81 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00021515 ECACC:00021515,
Wikidata:Q54830769
CVCL_9P81 2026-08-15 04:27:05 0
DD3555
 
Resource Report
Resource Website
RRID:CVCL_9N29 Homo sapiens (Human) Karyotypic information: 45,XY,der(14;21)(q10;q10)mat (ECACC=00062022)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:00062022,
Wikidata:Q54830804
CVCL_9N29 2026-08-15 04:27:06 0
DD3483
 
Resource Report
Resource Website
ECACC Cat# 99120702, RRID:CVCL_9N14 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99120702 ECACC:99120702,
Wikidata:Q54830764
CVCL_9N14 2026-08-15 04:27:06 0
DD3506
 
Resource Report
Resource Website
RRID:CVCL_9P83 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:00021518,
Wikidata:Q54830771
CVCL_9P83 2026-08-15 04:27:05 0
DD3517
 
Resource Report
Resource Website
ECACC Cat# 00030115, RRID:CVCL_9N17 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00030115 ECACC:00030115,
Wikidata:Q54830778
CVCL_9N17 2026-08-15 04:27:05 0
DD3506
 
Resource Report
Resource Website
ECACC Cat# 00021518, RRID:CVCL_9P83 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00021518 ECACC:00021518,
Wikidata:Q54830771
CVCL_9P83 2026-08-15 04:27:05 0
DD3521
 
Resource Report
Resource Website
ECACC Cat# 00031406, RRID:CVCL_9P90 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00031406 ECACC:00031406,
Wikidata:Q54830785
CVCL_9P90 2026-08-15 04:27:05 0
DD3560
 
Resource Report
Resource Website
ECACC Cat# 00070601, RRID:CVCL_9N30 Homo sapiens (Human) Karyotypic information: 46,XY,inv(6)(p24;q16.2); de novo (ECACC=00070601)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00070601 ECACC:00070601,
Wikidata:Q54830807
CVCL_9N30 2026-08-15 04:27:07 0
DD3522
 
Resource Report
Resource Website
RRID:CVCL_9N18 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:00031407,
Wikidata:Q54830786
CVCL_9N18 2026-08-15 04:27:05 0

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