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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
GM00738
 
Resource Report
Resource Website
RRID:CVCL_4J12 Homo sapiens (Human) Population: Caucasian. PMID:7803800 Finite cell line Male GM-738 CLO:CLO_0028813,
Coriell:GM00738,
Wikidata:Q54836432
CVCL_4J12 2026-08-15 04:28:52 0
GM00741
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX36 Homo sapiens (Human) Neuronal ceroid lipofuscinosis type 4B Finite cell line Male GM-741 Coriell:GM00741,
Wikidata:Q54836435
CVCL_CX36 2026-08-15 04:28:52 0
GM00754
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX51 Homo sapiens (Human) Finite cell line Female GM-754 Coriell:GM00754,
Wikidata:Q54836442
CVCL_CX51 2026-08-15 04:28:52 0
GM00773
 
Resource Report
Resource Website
RRID:CVCL_V781 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;7)(4qter->4p16::7q34->7qter;7pter->7q34::4p16->4pter) (Coriell=GM00773). PMID:891261 Finite cell line Female GM-773 CLO:CLO_0028839,
Coriell:GM00773,
Wikidata:Q54836450
CVCL_V781 2026-08-15 04:28:52 0
GM00878
 
Resource Report
Resource Website
RRID:CVCL_0R28 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-878 CLO:CLO_0029602,
Coriell:GM00878,
Wikidata:Q54836497
CVCL_0R28 2026-08-15 04:28:53 0
GM00861
 
Resource Report
Resource Website
RRID:CVCL_4D79 Homo sapiens (Human) Karyotypic information: 46,XY,ins(5;1)(5pter->5q15::1q25->1q32::5q15->5qter;1pter->1q25::1q32->1qter) (Coriell=GM00861)., Population: Caucasian. Finite cell line Male GM-861 CLO:CLO_0029634,
Coriell:GM00861,
Wikidata:Q54836482
CVCL_4D79 2026-08-15 04:28:53 0
GM00887
 
Resource Report
Resource Website
Coriell Cat# GM00887, RRID:CVCL_V530 Homo sapiens (Human) Hurler syndrome Population: Caucasian. PMID:8328452 Finite cell line Female GM-887, GM 00887 Coriell GM00887 CLO:CLO_0029583,
Coriell:GM00887,
Wikidata:Q54836510
CVCL_V530 2026-08-15 04:28:53 0
GM00851
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB84 Homo sapiens (Human) Cystic fibrosis Finite cell line Male GM-851 Coriell:GM00851,
Wikidata:Q54836474
CVCL_JB84 2026-08-15 04:28:53 0
GM00903
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00903, RRID:CVCL_CX34 Homo sapiens (Human) Mucopolysaccharidosis type IIIA Finite cell line Male GM-903 Coriell GM00903 Coriell:GM00903,
Wikidata:Q54836521
CVCL_CX34 2026-08-15 04:28:54 0
GM00847
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7908 Homo sapiens (Human) Lesch-Nyhan syndrome Characteristics: Cell line positive for alternative lengthening of telomeres (ALT+) (CelloPub=CLPUB00712; PubMed=19935656)., Population: African American. PMID:174085
PMID:191830
PMID:1260760
PMID:3413074
PMID:9175740
PMID:11359895
PMID:12361951
PMID:19935656
PMID:26001292
Transformed cell line Male LN-SV, LNSV, GM-847, GM 847, GM847 CLO:CLO_0029655,
EFO:EFO_0022519,
Coriell:GM00847,
Wikidata:Q54836472
cvcl_f127 CVCL_7908 2026-08-15 04:28:53 5
GM00851
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00851, RRID:CVCL_JB84 Homo sapiens (Human) Cystic fibrosis Finite cell line Male GM-851 Coriell GM00851 Coriell:GM00851,
Wikidata:Q54836474
CVCL_JB84 2026-08-15 04:28:53 0
GM00867
 
Resource Report
Resource Website
RRID:CVCL_2H07 Homo sapiens (Human) Homocystinuria Finite cell line Male GM0867, GM-867 CLO:CLO_0029636,
Coriell:GM00867,
Wikidata:Q54836489
CVCL_2H07 2026-08-15 04:28:53 0
GM00882
 
Resource Report
Resource Website
RRID:CVCL_0Q46 Homo sapiens (Human) Fabry disease Population: Caucasian; Italian. PMID:29982630 Finite cell line Male GM-882 CLO:CLO_0029628,
Coriell:GM00882,
Wikidata:Q54836506
CVCL_0Q46 2026-08-15 04:28:53 0
GM00845
 
Resource Report
Resource Website
Coriell Cat# GM00845, RRID:CVCL_V782 Homo sapiens (Human) Karyotypic information: 46,XX,t(2;8)(2pter->2q37::8q13->8qter;8pter->8q13::2q37->2qter)mat (Coriell=GM00845)., Population: Caucasian. PMID:648194 Finite cell line Female GM-845 Coriell GM00845 CLO:CLO_0029652,
Coriell:GM00845,
Wikidata:Q54836470
CVCL_V782 2026-08-15 04:28:53 0
GM00870
 
Resource Report
Resource Website
RRID:CVCL_V784 Homo sapiens (Human) Intellectual developmental disorder Population: Caucasian. PMID:1017321
PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-870, GM-0870, GM 870 CLO:CLO_0029601,
Coriell:GM00870,
Wikidata:Q54836493
CVCL_V784 2026-08-15 04:28:53 0
GM00902
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX33 Homo sapiens (Human) Finite cell line Female GM-902 Coriell:GM00902,
Wikidata:Q54836520
CVCL_CX33 2026-08-15 04:28:54 0
GM00893
 
Resource Report
Resource Website
Coriell Cat# GM17208, RRID:CVCL_7306 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:16260726
PMID:20889555
PMID:22152194
PMID:29959025
Transformed cell line Female GM-893, GM00893A, GM17208 Coriell GM17208 CLO:CLO_0013884,
CLO:CLO_0029581,
Coriell:GM00893,
Coriell:GM17208,
GEO:GSM569509,
GEO:GSM596272,
GEO:GSM596633,
GEO:GSM924810,
Wikidata:Q54836515
CVCL_7306 2026-08-15 04:28:54 0
GM00804
 
Resource Report
Resource Website
Coriell Cat# GM00804, RRID:CVCL_H175 Homo sapiens (Human) Nephropathic cystinosis Finite cell line Male GM-804 Coriell GM00804 CLO:CLO_0029644,
Coriell:GM00804,
Wikidata:Q54836463
CVCL_H175 2026-08-15 04:28:52 0
GM00802
 
Resource Report
Resource Website
Coriell Cat# GM00802, RRID:CVCL_1B70 Homo sapiens (Human) Fucosidosis PMID:4074382 Finite cell line Male GM-802, GM 802, GM802 Coriell GM00802 CLO:CLO_0028847,
Coriell:GM00802,
Wikidata:Q54836461
CVCL_1B70 2026-08-15 04:28:52 0
GM00805
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00805, RRID:CVCL_JD85 Homo sapiens (Human) Finite cell line Male GM-805 Coriell GM00805 Coriell:GM00805,
Wikidata:Q54836464
CVCL_JD85 2026-08-15 04:28:53 0

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