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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
GM02027
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB69 Homo sapiens (Human) Finite cell line Female GM-2027 Coriell:GM02027,
Wikidata:Q54837246
CVCL_JB69 2026-07-25 04:32:27 0
GM02054
 
Resource Report
Resource Website
Coriell Cat# GM02054, RRID:CVCL_X087 Homo sapiens (Human) PMID:6617268
PMID:6661932
Transformed cell line Male GM-2054, GM 2054 Coriell GM02054 CLO:CLO_0032538,
BioSample:SAMN00807438,
Coriell:GM02054,
Wikidata:Q54837273
CVCL_X087 2026-07-25 04:32:28 0
GM02030
 
Resource Report
Resource Website
Coriell Cat# GM02030, RRID:CVCL_X259 Homo sapiens (Human) Trisomy 8 Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM-2030, GM 2030 Coriell GM02030 CLO:CLO_0032576,
BioSample:SAMN00807404,
Coriell:GM02030,
Wikidata:Q54837249
CVCL_X259 2026-07-25 04:32:28 0
GM02048
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_M927 Homo sapiens (Human) Mucolipidosis type IV Population: Jewish; Ashkenazi. Finite cell line Female GM-2048 CLO:CLO_0032549,
BioSample:SAMN00807426,
Coriell:GM02048,
Wikidata:Q54837263
CVCL_M927 2026-07-25 04:32:28 2
GM02067
 
Resource Report
Resource Website
Coriell Cat# GM02067, RRID:CVCL_V467 Homo sapiens (Human) Down syndrome Karyotypic information: 47,XY,+21 [44]; 47,XY,t(1;16)(q21;p13.3],+21 [4]; 46,XY [2] (Coriell=GM02067)., Population: Caucasian. PMID:6661932 Finite cell line Male GM-2067, GM 2067, GM02067A Coriell GM02067 CLO:CLO_0032517,
BioSample:SAMN00807456,
Coriell:GM02067,
Wikidata:Q54837284
CVCL_V467 2026-07-25 04:32:28 0
GM02044
 
Resource Report
Resource Website
RRID:CVCL_1D93 Homo sapiens (Human) Karyotypic information: 45,XY,-16,t(14;16)(16;18)(14qter->14p12::16p11->16pter;18qter->18p1::16q12->16qter) (Coriell=GM02044). PMID:2095701 Finite cell line Male GM-2044, GM2044 CLO:CLO_0032556,
Coriell:GM02044,
Wikidata:Q54837259
CVCL_1D93 2026-07-25 04:32:28 0
GM02099
 
Resource Report
Resource Website
RRID:CVCL_2Z73 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Population: Caucasian. Transformed cell line Male GM-2099 CLO:CLO_0031823,
BioSample:SAMN00807488,
Coriell:GM02099,
Wikidata:Q54837302
CVCL_2Z73 2026-07-25 04:32:29 0
GM02124
 
Resource Report
Resource Website
RRID:CVCL_4J45 Homo sapiens (Human) Acute intermittent porphyria Population: Caucasian. Transformed cell line Female GM-2124 CLO:CLO_0031847,
BioSample:SAMN00807498,
Coriell:GM02124,
Wikidata:Q54837308
CVCL_4J45 2026-07-25 04:32:29 0
GM02068
 
Resource Report
Resource Website
RRID:CVCL_1N60 Homo sapiens (Human) Karyotypic information: 46,XX,t(6;7)(6pter->6q27::7q22->7qter;7pter->7q22::6q27->6qter) (Coriell=GM02068)., Population: Caucasian. Finite cell line Female GM-2068 CLO:CLO_0032518,
BioSample:SAMN00807458,
Coriell:GM02068,
Wikidata:Q54837285
CVCL_1N60 2026-07-25 04:32:28 0
GM02047
 
Resource Report
Resource Website
RRID:CVCL_L762 Homo sapiens (Human) Population: Caucasian. PMID:16465621 Finite cell line Male GM-2047 CLO:CLO_0032558,
BioSample:SAMN00807424,
Coriell:GM02047,
Wikidata:Q54837262
CVCL_L762 2026-07-25 04:32:28 0
GM02052+hTERT
 
Resource Report
Resource Website
RRID:CVCL_VL09 Homo sapiens (Human) Ataxia telangiectasia syndrome Population: Jewish; Moroccan. PMID:11313956 Telomerase immortalized cell line Female hTERT+ GM02052 Wikidata:Q93575552 cvcl_7350 CVCL_VL09 2026-07-25 04:32:28 0
GM02037
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7349 Homo sapiens (Human) Karyotypic information: 46,XY [45]; 46,XY,t(4;16)(4qter->4p14::16q24->16qter;16pter->16q24::4p14->4pter) [5] (Coriell=GM02037)., Population: Caucasian. PMID:6223188
PMID:8643543
PMID:30567591
Finite cell line Male GM2037, GM-2037, GM 2037, GM02037A, GM2037A, GM 2037A, GM02037B, GM 2037B, GM02037C BTO:BTO_0003842,
CLO:CLO_0032574,
BioSample:SAMN00807416,
Coriell:GM02037,
GEO:GSM3124641,
Wikidata:Q54837256
CVCL_7349 2026-07-25 04:32:28 1
GM02074
 
Resource Report
Resource Website
RRID:CVCL_0P00 Homo sapiens (Human) Population: African American. Finite cell line Female GM-2074 CLO:CLO_0032512,
BioSample:SAMN00807460,
Coriell:GM02074,
Wikidata:Q54837287
CVCL_0P00 2026-07-25 04:32:28 0
GM02017
 
Resource Report
Resource Website
RRID:CVCL_M992 Homo sapiens (Human) Population: Arab., Part of: Human variation panel. PMID:8328452 Finite cell line Male GM-2017, GM 02017, GM17333 CLO:CLO_0013617,
CLO:CLO_0032316,
BioSample:SAMN00807392,
Coriell:GM02017,
Coriell:GM17333,
Wikidata:Q54837240
CVCL_M992 2026-07-25 04:32:28 0
GM02038
 
Resource Report
Resource Website
Coriell Cat# GM02038, RRID:CVCL_CW68 Homo sapiens (Human) Schizophrenia Population: Caucasian. PMID:7847674
PMID:21490598
Finite cell line Male GM-2038 Coriell GM02038 CLO:CLO_0032554,
BioSample:SAMN00807418,
Coriell:GM02038,
Wikidata:Q54837257
CVCL_CW68 2026-07-25 04:32:28 0
GM02121
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM02121, RRID:CVCL_JB66 Homo sapiens (Human) Finite cell line Female GM-2121 Coriell GM02121 Coriell:GM02121,
Wikidata:Q54837306
CVCL_JB66 2026-07-25 04:32:29 0
GM02054
 
Resource Report
Resource Website
RRID:CVCL_X087 Homo sapiens (Human) PMID:6617268
PMID:6661932
Transformed cell line Male GM-2054, GM 2054 CLO:CLO_0032538,
BioSample:SAMN00807438,
Coriell:GM02054,
Wikidata:Q54837273
CVCL_X087 2026-07-25 04:32:29 0
GM02055
 
Resource Report
Resource Website
Coriell Cat# GM02055, RRID:CVCL_H177 Homo sapiens (Human) PMID:6617268 Finite cell line Female GM-2055, GM 2055 Coriell GM02055 CLO:CLO_0032535,
Coriell:GM02055,
Wikidata:Q54837274
CVCL_H177 2026-07-25 04:32:29 0
GM02110
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01450, RRID:CVCL_L962 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Transformed cell line Male GM-2110, GM02110A, GM01450, GM-1450 Coriell GM01450 CLO:CLO_0031830,
BioSample:SAMN00807494,
Coriell:GM01450,
Coriell:GM02110,
Wikidata:Q54837305
CVCL_L962 2026-07-25 04:32:29 0
GM02110
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L962 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Transformed cell line Male GM-2110, GM02110A, GM01450, GM-1450 CLO:CLO_0031830,
BioSample:SAMN00807494,
Coriell:GM01450,
Coriell:GM02110,
Wikidata:Q54837305
CVCL_L962 2026-07-25 04:32:29 0

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