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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
GM13321
 
Resource Report
Resource Website
Coriell Cat# GM17174, RRID:CVCL_N207 Homo sapiens (Human) Population: African American., Part of: Human variation panel. PMID:16260726
PMID:23665875
Transformed cell line Male GM17174 Coriell GM17174 CLO:CLO_0013224,
CLO:CLO_0014034,
BioSample:SAMN00802297,
Coriell:GM13321,
Coriell:GM17174,
GEO:GSM569746,
GEO:GSM596238,
GEO:GSM597033,
GEO:GSM924684,
Wikidata:Q54846458
CVCL_N207 2026-08-15 04:31:54 0
GM13423
 
Resource Report
Resource Website
RRID:CVCL_0N24 Homo sapiens (Human) Cystic fibrosis PMID:19359498 Transformed cell line Female CLO:CLO_0012643,
BioSample:SAMN00802358,
Coriell:GM13423,
Wikidata:Q54846516
CVCL_0N24 2026-08-15 04:31:55 0
GM13395
 
Resource Report
Resource Website
RRID:CVCL_JF49 Homo sapiens (Human) 5' 10' methylenetetrahydrofolate reductase deficiency Population: Arab; Saudi Arabian., From: Montreal Children's Hospital cell repository; Montreal; Canada. PMID:8940272 Finite cell line Female WG2255, 2255 CLO:CLO_0012849,
BioSample:SAMN00802340,
Coriell:GM13395,
Wikidata:Q54846505
CVCL_JF49 2026-08-15 04:31:55 0
GM13425
 
Resource Report
Resource Website
RRID:CVCL_AN08 Homo sapiens (Human) Ehlers-Danlos syndrome, type VI Population: Caucasian. Finite cell line Male CLO:CLO_0012644,
BioSample:SAMN00802360,
Coriell:GM13425,
Wikidata:Q54846517
CVCL_AN08 2026-08-15 04:31:55 0
GM13409
 
Resource Report
Resource Website
RRID:CVCL_1K76 Homo sapiens (Human) Glycogen storage disease type II Transformed cell line Female BioSample:SAMN00802344,
Coriell:GM13409,
Wikidata:Q54846507
CVCL_1K76 2026-08-15 04:31:55 0
GM13418
 
Resource Report
Resource Website
RRID:CVCL_N208 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM17299 CLO:CLO_0012645,
CLO:CLO_0013115,
BioSample:SAMN00802354,
Coriell:GM13418,
Coriell:GM17299,
Wikidata:Q54846514
CVCL_N208 2026-08-15 04:31:55 0
GM13440
 
Resource Report
Resource Website
Coriell Cat# GM13440, RRID:CVCL_CX13 Homo sapiens (Human) Glycine encephalopathy Population: Jordanian. Finite cell line Female Coriell GM13440 CLO:CLO_0012667,
BioSample:SAMN00802378,
Coriell:GM13440,
Wikidata:Q54846530
CVCL_CX13 2026-08-15 04:31:55 0
GM13408
 
Resource Report
Resource Website
RRID:CVCL_1K75 Homo sapiens (Human) Glycogen storage disease type II Transformed cell line Female BioSample:SAMN00802342,
Coriell:GM13408,
Wikidata:Q54846506
CVCL_1K75 2026-08-15 04:31:55 0
GM13315
 
Resource Report
Resource Website
RRID:CVCL_4F11 Homo sapiens (Human) Ellis-Van Creveld syndrome Population: Caucasian; Amish. Transformed cell line Female CLO:CLO_0013219,
BioSample:SAMN00802295,
Coriell:GM13315,
Wikidata:Q54846456
CVCL_4F11 2026-08-15 04:31:54 0
GM13418
 
Resource Report
Resource Website
Coriell Cat# GM13418, RRID:CVCL_N208 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM17299 Coriell GM13418 CLO:CLO_0012645,
CLO:CLO_0013115,
BioSample:SAMN00802354,
Coriell:GM13418,
Coriell:GM17299,
Wikidata:Q54846514
CVCL_N208 2026-08-15 04:31:59 0
GM13356
 
Resource Report
Resource Website
Coriell Cat# GM13356, RRID:CVCL_0I46 Homo sapiens (Human) Part of: CEPH/Venezuelan pedigree cell line collection. Transformed cell line Female Coriell GM13356 CLO:CLO_0012842,
Coriell:GM13356,
Wikidata:Q54846480
CVCL_0I46 2026-08-15 04:31:55 0
GM13325
 
Resource Report
Resource Website
RRID:CVCL_2Y99 Homo sapiens (Human) 22q11.2 deletion syndrome Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0013273,
BioSample:SAMN00802301,
Coriell:GM13325,
Wikidata:Q54846462
CVCL_2Y99 2026-08-15 04:31:55 0
GM13440
 
Resource Report
Resource Website
RRID:CVCL_CX13 Homo sapiens (Human) Glycine encephalopathy Population: Jordanian. Finite cell line Female CLO:CLO_0012667,
BioSample:SAMN00802378,
Coriell:GM13440,
Wikidata:Q54846530
CVCL_CX13 2026-08-15 04:31:55 0
GM13428
 
Resource Report
Resource Website
RRID:CVCL_IJ40 Homo sapiens (Human) MASA syndrome Transformed cell line Male CLO:CLO_0012672,
BioSample:SAMN00802366,
Coriell:GM13428,
Wikidata:Q54846520
CVCL_IJ40 2026-08-15 04:31:55 0
GM13468
 
Resource Report
Resource Website
Coriell Cat# GM13468, RRID:CVCL_5P88 Homo sapiens (Human) Williams syndrome Population: Caucasian. Transformed cell line Male Coriell GM13468 CLO:CLO_0012222,
BioSample:SAMN00802398,
Coriell:GM13468,
Wikidata:Q54846548
CVCL_5P88 2026-08-15 04:32:00 0
GM13472
 
Resource Report
Resource Website
RRID:CVCL_5P91 Homo sapiens (Human) Williams syndrome Population: Caucasian. Transformed cell line Female CLO:CLO_0012212,
BioSample:SAMN00802404,
Coriell:GM13472,
Wikidata:Q54846559
CVCL_5P91 2026-08-15 04:31:56 0
GM13512
 
Resource Report
Resource Website
RRID:CVCL_1J79 Homo sapiens (Human) Huntington's disease Transformed cell line Female CLO:CLO_0012411,
Coriell:GM13512,
Wikidata:Q54846598
CVCL_1J79 2026-08-15 04:32:01 0
GM13468
 
Resource Report
Resource Website
RRID:CVCL_5P88 Homo sapiens (Human) Williams syndrome Population: Caucasian. Transformed cell line Male CLO:CLO_0012222,
BioSample:SAMN00802398,
Coriell:GM13468,
Wikidata:Q54846548
CVCL_5P88 2026-08-15 04:31:56 0
GM13461
 
Resource Report
Resource Website
Coriell Cat# GM13461, RRID:CVCL_5P82 Homo sapiens (Human) Williams syndrome Population: Caucasian. PMID:23665875 Transformed cell line Male Coriell GM13461 CLO:CLO_0012170,
BioSample:SAMN00802386,
Coriell:GM13461,
Wikidata:Q54846540
CVCL_5P82 2026-08-15 04:32:00 0
GM13502
 
Resource Report
Resource Website
Coriell Cat# GM13502, RRID:CVCL_DE55 Homo sapiens (Human) Group: Human/rodent somatic cell hybrid. Hybrid cell line D6S5 Coriell GM13502 CLO:CLO_0012368,
Coriell:GM13502,
Wikidata:Q54846588
cvcl_4032 CVCL_DE55 2026-08-15 04:31:57 0

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