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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
DD3505
 
Resource Report
Resource Website
ECACC Cat# 00021517, RRID:CVCL_9P82 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00021517 ECACC:00021517,
Wikidata:Q54830770
CVCL_9P82 2026-07-25 04:30:15 0
DD3514
 
Resource Report
Resource Website
ECACC Cat# 00022829, RRID:CVCL_9P87 Homo sapiens (Human) Karyotypic information: 69,XXX; 46,XY (ECACC=00022829)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00022829 ECACC:00022829,
Wikidata:Q54830777
CVCL_9P87 2026-07-25 04:30:15 0
DD3581
 
Resource Report
Resource Website
ECACC Cat# 00092208, RRID:CVCL_9N34 Homo sapiens (Human) Karyotypic information: 46,XX,inv(13)t(13;18)(q31.2;q32.3)(q32.3;q23)mat (ECACC=00092208)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 00092208 ECACC:00092208,
Wikidata:Q54830814
CVCL_9N34 2026-07-25 04:30:16 0
DD3662
 
Resource Report
Resource Website
ECACC Cat# 01052222, RRID:CVCL_9Q15 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 01052222 ECACC:01052222,
Wikidata:Q54830848
CVCL_9Q15 2026-07-25 04:30:18 0
DD3635
 
Resource Report
Resource Website
ECACC Cat# 01020503, RRID:CVCL_9N47 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 01020503 ECACC:01020503,
Wikidata:Q54830838
CVCL_9N47 2026-07-25 04:30:17 0
DD3589
 
Resource Report
Resource Website
ECACC Cat# 00101122, RRID:CVCL_9N37 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00101122 ECACC:00101122,
Wikidata:Q54830818
CVCL_9N37 2026-07-25 04:30:17 0
DD3637
 
Resource Report
Resource Website
ECACC Cat# 01021301, RRID:CVCL_9N48 Homo sapiens (Human) Aniridia Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 01021301 ECACC:01021301,
Wikidata:Q54830839
CVCL_9N48 2026-07-25 04:30:17 0
DD3619
 
Resource Report
Resource Website
ECACC Cat# 01010201, RRID:CVCL_9Q09 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 01010201 ECACC:01010201,
Wikidata:Q54830832
CVCL_9Q09 2026-07-25 04:30:17 0
DD3625
 
Resource Report
Resource Website
ECACC Cat# 01011217, RRID:CVCL_9N44 Homo sapiens (Human) Karyotypic information: 46,XX,inv(9)(q?13;q22.33)pat (ECACC=01011217)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 01011217 ECACC:01011217,
Wikidata:Q54830834
CVCL_9N44 2026-07-25 04:30:17 0
DD3593
 
Resource Report
Resource Website
ECACC Cat# 00102515, RRID:CVCL_9Q05 Homo sapiens (Human) Developmental delay Karyotypic information: 46,XY,add(1)(p36.3) (ECACC=00102515)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00102515 ECACC:00102515,
Wikidata:Q54830820
CVCL_9Q05 2026-07-25 04:30:17 0
DD3686
 
Resource Report
Resource Website
ECACC Cat# 01080715, RRID:CVCL_9Q23 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 01080715 ECACC:01080715,
Wikidata:Q54830859
CVCL_9Q23 2026-07-25 04:30:18 0
DD3639
 
Resource Report
Resource Website
ECACC Cat# 01021303, RRID:CVCL_9N50 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 01021303 ECACC:01021303,
Wikidata:Q54830841
CVCL_9N50 2026-07-25 04:30:17 0
DD3579
 
Resource Report
Resource Website
ECACC Cat# 00092101, RRID:CVCL_9Q02 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00092101 ECACC:00092101,
Wikidata:Q54830813
CVCL_9Q02 2026-07-25 04:30:16 0
DD3665
 
Resource Report
Resource Website
ECACC Cat# 01052513, RRID:CVCL_9Q17 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 01052513 ECACC:01052513,
Wikidata:Q54830850
CVCL_9Q17 2026-07-25 04:30:17 0
DD3615
 
Resource Report
Resource Website
ECACC Cat# 00122017, RRID:CVCL_9Q07 Homo sapiens (Human) Developmental delay Karyotypic information: 46,XY,t(7;13)(q31.3;q21.3); de novo, inv(11)(p15.3;p15.5)pat (ECACC=00122017)., Part of: ECACC chromosomal abnormality collection. PMID:15635069 Transformed cell line Male ECACC 00122017 ECACC:00122017,
Wikidata:Q54830829
CVCL_9Q07 2026-07-25 04:30:17 0
DD3572
 
Resource Report
Resource Website
ECACC Cat# 00081101, RRID:CVCL_9N31 Homo sapiens (Human) Karyotypic information: 46,XY,t(2;7) (ECACC=00081101)., Part of: ECACC chromosomal abnormality collection. PMID:15635069 Transformed cell line Male ECACC 00081101 ECACC:00081101,
Wikidata:Q54830809
CVCL_9N31 2026-07-25 04:30:16 0
DD3685
 
Resource Report
Resource Website
ECACC Cat# 01072513, RRID:CVCL_9Q22 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 01072513 ECACC:01072513,
Wikidata:Q54830858
CVCL_9Q22 2026-07-25 04:30:18 0
DD3638
 
Resource Report
Resource Website
ECACC Cat# 01021302, RRID:CVCL_9N49 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 01021302 ECACC:01021302,
Wikidata:Q54830840
CVCL_9N49 2026-07-25 04:30:17 0
DD3611
 
Resource Report
Resource Website
ECACC Cat# 00112921, RRID:CVCL_9N41 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 00112921 ECACC:00112921,
Wikidata:Q54830828
CVCL_9N41 2026-07-25 04:30:17 0
DD3590
 
Resource Report
Resource Website
ECACC Cat# 00101217, RRID:CVCL_9Q04 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00101217 ECACC:00101217,
Wikidata:Q54830819
CVCL_9Q04 2026-07-25 04:30:17 0

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