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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
DD0651
 
Resource Report
Resource Website
ECACC Cat# 92022808, RRID:CVCL_9B22 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022808 ECACC:92022808,
Wikidata:Q54829170
CVCL_9B22 2026-07-25 04:29:33 0
DD0689
 
Resource Report
Resource Website
ECACC Cat# 92033007, RRID:CVCL_9B44 Homo sapiens (Human) Congenital hydrocephalus Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92033007 ECACC:92033007,
Wikidata:Q54829200
CVCL_9B44 2026-07-25 04:29:35 0
DD0698
 
Resource Report
Resource Website
ECACC Cat# 92040904, RRID:CVCL_9B47 Homo sapiens (Human) Klinefelter syndrome Karyotypic information: 47,XXY (ECACC=92040904)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92040904 ECACC:92040904,
Wikidata:Q54829203
CVCL_9B47 2026-07-25 04:29:35 0
DD0693
 
Resource Report
Resource Website
ECACC Cat# 92040308, RRID:CVCL_9B45 Homo sapiens (Human) Karyotypic information: 46,XX,t(13;18)(q22;q21.3)(?O) (ECACC=92040308)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92040308 ECACC:92040308,
Wikidata:Q54829201
CVCL_9B45 2026-07-25 04:29:34 0
DD0696
 
Resource Report
Resource Website
ECACC Cat# 92040902, RRID:CVCL_9B46 Homo sapiens (Human) Karyotypic information: 46,XX,del(18)(pter->q21.1); de novo (ECACC=92040902)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92040902 ECACC:92040902,
Wikidata:Q54829202
CVCL_9B46 2026-07-25 04:29:34 0
DD0665
 
Resource Report
Resource Website
ECACC Cat# 92030642, RRID:CVCL_9B29 Homo sapiens (Human) Karyotypic information: 46,XY,t(1;13)(p22;q32)(?O) (ECACC=92030642)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92030642 ECACC:92030642,
Wikidata:Q54829177
CVCL_9B29 2026-07-25 04:29:35 0
DD0664
 
Resource Report
Resource Website
ECACC Cat# 92030625, RRID:CVCL_9B28 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92030625 ECACC:92030625,
Wikidata:Q54829176
CVCL_9B28 2026-07-25 04:29:33 0
DD0671
 
Resource Report
Resource Website
ECACC Cat# 92031101, RRID:CVCL_9B33 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92031101 ECACC:92031101,
Wikidata:Q54829188
CVCL_9B33 2026-07-25 04:29:33 0
DD0649
 
Resource Report
Resource Website
ECACC Cat# 92022806, RRID:CVCL_9B20 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92022806 ECACC:92022806,
Wikidata:Q54829168
CVCL_9B20 2026-07-25 04:29:35 0
DD0667
 
Resource Report
Resource Website
ECACC Cat# 92030644, RRID:CVCL_9B31 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92030644 ECACC:92030644,
Wikidata:Q54829179
CVCL_9B31 2026-07-25 04:29:33 0
DD0638
 
Resource Report
Resource Website
ECACC Cat# 92022114, RRID:CVCL_9B14 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92022114 ECACC:92022114,
Wikidata:Q54829161
CVCL_9B14 2026-07-25 04:29:35 0
DD0645
 
Resource Report
Resource Website
ECACC Cat# 92022802, RRID:CVCL_9B16 Homo sapiens (Human) Turner syndrome Karyotypic information: 45,X0 (ECACC=92022802)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92022802 ECACC:92022802,
Wikidata:Q54829163
CVCL_9B16 2026-07-25 04:29:33 0
DD0704
 
Resource Report
Resource Website
ECACC Cat# 92041020, RRID:CVCL_9B50 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92041020 ECACC:92041020,
Wikidata:Q54829206
CVCL_9B50 2026-07-25 04:29:35 0
DD0758
 
Resource Report
Resource Website
ECACC Cat# 92051807, RRID:CVCL_9B87 Homo sapiens (Human) Karyotypic information: 46,XY,inv(13)(q21.3;q22.3)mat (ECACC=92051807)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92051807 ECACC:92051807,
Wikidata:Q54829260
CVCL_9B87 2026-07-25 04:29:35 0
DD0765
 
Resource Report
Resource Website
ECACC Cat# 92052206, RRID:CVCL_9B93 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92052206 ECACC:92052206,
Wikidata:Q54829267
CVCL_9B93 2026-07-25 04:29:35 0
DD0742
 
Resource Report
Resource Website
ECACC Cat# 92043038, RRID:CVCL_9B76 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92043038 ECACC:92043038,
Wikidata:Q54829246
CVCL_9B76 2026-07-25 04:29:35 0
DD0733
 
Resource Report
Resource Website
ECACC Cat# 92043029, RRID:CVCL_9B70 Homo sapiens (Human) Karyotypic information: 46,XX,del(13)(q21)?(q21.1 or q21.2) (ECACC=92043029)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92043029 ECACC:92043029,
Wikidata:Q54829226
CVCL_9B70 2026-07-25 04:29:34 0
DD0769
 
Resource Report
Resource Website
ECACC Cat# 92052210, RRID:CVCL_9B96 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92052210 ECACC:92052210,
Wikidata:Q54829270
CVCL_9B96 2026-07-25 04:29:35 0
DD0745
 
Resource Report
Resource Website
ECACC Cat# 92050718, RRID:CVCL_9B78 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92050718 ECACC:92050718,
Wikidata:Q54829248
CVCL_9B78 2026-07-25 04:29:36 0
DD0766
 
Resource Report
Resource Website
ECACC Cat# 92052207, RRID:CVCL_9B94 Homo sapiens (Human) Karyotypic information: 46,XY,t(5;10)(q35.1;q26.3)mat (ECACC=92052207)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92052207 ECACC:92052207,
Wikidata:Q54829268
CVCL_9B94 2026-07-25 04:29:35 0

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