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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
DD0429
 
Resource Report
Resource Website
ECACC Cat# 91090401, RRID:CVCL_8Z94 Homo sapiens (Human) Karyotypic information: 46,XX,inv(7)(q22.1;q34) (ECACC=91090401)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91090401 ECACC:91090401,
Wikidata:Q54829020
CVCL_8Z94 2026-07-25 04:29:29 0
DD0407
 
Resource Report
Resource Website
ECACC Cat# 91081610, RRID:CVCL_8Z80 Homo sapiens (Human) Treacher Collins syndrome Karyotypic information: 46,XY,t(2;13)(q33;q?32) (ECACC=91081610)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 91081610 ECACC:91081610,
Wikidata:Q54829003
CVCL_8Z80 2026-07-25 04:29:29 0
DD0410
 
Resource Report
Resource Website
ECACC Cat# 91082012, RRID:CVCL_8Z83 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91082012 ECACC:91082012,
Wikidata:Q54829007
CVCL_8Z83 2026-07-25 04:29:29 0
DD0411
 
Resource Report
Resource Website
ECACC Cat# 91082013, RRID:CVCL_8Z84 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91082013 ECACC:91082013,
Wikidata:Q54829008
CVCL_8Z84 2026-07-25 04:29:31 0
DD0384
 
Resource Report
Resource Website
ECACC Cat# 91080106, RRID:CVCL_8Z62 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91080106 ECACC:91080106,
Wikidata:Q54828978
CVCL_8Z62 2026-07-25 04:29:28 0
DD0375
 
Resource Report
Resource Website
ECACC Cat# 91072919, RRID:CVCL_8Z53 Homo sapiens (Human) Karyotypic information: 46,XX [22]; 47,XX,+mar(19) [28] (ECACC=91072919)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91072919 ECACC:91072919,
Wikidata:Q54828969
CVCL_8Z53 2026-07-25 04:29:28 0
DD0417
 
Resource Report
Resource Website
ECACC Cat# 91082315, RRID:CVCL_8Z87 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91082315 ECACC:91082315,
Wikidata:Q54829012
CVCL_8Z87 2026-07-25 04:29:31 0
DD0423
 
Resource Report
Resource Website
ECACC Cat# 91082804, RRID:CVCL_8Z90 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91082804 ECACC:91082804,
Wikidata:Q54829015
CVCL_8Z90 2026-07-25 04:29:31 0
DD0415
 
Resource Report
Resource Website
ECACC Cat# 91082203, RRID:CVCL_8Z85 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91082203 ECACC:91082203,
Wikidata:Q54829009
CVCL_8Z85 2026-07-25 04:29:29 0
DD0424
 
Resource Report
Resource Website
ECACC Cat# 91083005, RRID:CVCL_8Z91 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91083005 ECACC:91083005,
Wikidata:Q54829017
CVCL_8Z91 2026-07-25 04:29:29 0
DD0435
 
Resource Report
Resource Website
ECACC Cat# 91090616, RRID:CVCL_9A05 Homo sapiens (Human) Karyotypic information: 46,XX,inv(3p) (ECACC=91090616)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91090616 ECACC:91090616,
Wikidata:Q54829027
CVCL_9A05 2026-07-25 04:29:29 0
DD0391
 
Resource Report
Resource Website
ECACC Cat# 91080502, RRID:CVCL_8Z69 Homo sapiens (Human) Karyotypic information: 46,XY,inv(6)(p21.3;?q22),t(6;17)(?q22;q23); de novo (ECACC=91080502)., Part of: ECACC chromosomal abnormality collection. PMID:15635069 Transformed cell line Male ECACC 91080502 ECACC:91080502,
Wikidata:Q54828991
CVCL_8Z69 2026-07-25 04:29:31 0
DD0418
 
Resource Report
Resource Website
ECACC Cat# 91082816, RRID:CVCL_8Z88 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91082816 ECACC:91082816,
Wikidata:Q54829013
CVCL_8Z88 2026-07-25 04:29:29 0
DD0382
 
Resource Report
Resource Website
ECACC Cat# 91080104, RRID:CVCL_8Z60 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91080104 ECACC:91080104,
Wikidata:Q54828976
CVCL_8Z60 2026-07-25 04:29:30 0
DD0433
 
Resource Report
Resource Website
ECACC Cat# 91090614, RRID:CVCL_9A03 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91090614 ECACC:91090614,
Wikidata:Q54829025
CVCL_9A03 2026-07-25 04:29:29 0
DD0404
 
Resource Report
Resource Website
ECACC Cat# 91081410, RRID:CVCL_8Z78 Homo sapiens (Human) Turner syndrome Karyotypic information: 45,X0 (ECACC=91081410)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 91081410 ECACC:91081410,
Wikidata:Q54829001
CVCL_8Z78 2026-07-25 04:29:31 0
DD0440
 
Resource Report
Resource Website
ECACC Cat# 91090919, RRID:CVCL_9A07 Homo sapiens (Human) Karyotypic information: 46,XX-6,der(6)t(4;6)(q27;p25)mat (ECACC=91090919)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 91090919 ECACC:91090919,
Wikidata:Q54829030
CVCL_9A07 2026-07-25 04:29:32 0
DD0496
 
Resource Report
Resource Website
ECACC Cat# 91103002, RRID:CVCL_9A40 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91103002 ECACC:91103002,
Wikidata:Q54829074
CVCL_9A40 2026-07-25 04:29:33 0
DD0442
 
Resource Report
Resource Website
ECACC Cat# 91091202, RRID:CVCL_9A08 Homo sapiens (Human) Fragile X syndrome Karyotypic information: 46,XY,fra(X)(q28) 15% fra(X) +ve (ECACC=91091202)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 91091202 ECACC:91091202,
Wikidata:Q54829031
CVCL_9A08 2026-07-25 04:29:30 0
DD0483
 
Resource Report
Resource Website
ECACC Cat# 91101623, RRID:CVCL_9A31 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 91101623 ECACC:91101623,
Wikidata:Q54829065
CVCL_9A31 2026-07-25 04:29:33 0

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