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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 Authority Record Last Update Mentions Count
GM04081
 
Resource Report
Resource Website
RRID:CVCL_0R01 Homo sapiens (Human) Primary carnitine deficiency Population: Caucasian. Finite cell line Male CLO:CLO_0016224,
Coriell:GM04081,
Wikidata:Q54838384
CVCL_0R01 Cellosaurus 2026-09-26 06:49:13 0
GM04126
 
Resource Report
Resource Website
RRID:CVCL_V820 Homo sapiens (Human) Wolf-Hirschhorn syndrome Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM 4126 CLO:CLO_0016204,
Coriell:GM04126,
Wikidata:Q54838392
CVCL_V820 Cellosaurus 2026-09-26 06:49:13 0
GM04079
 
Resource Report
Resource Website
RRID:CVCL_T821 Homo sapiens (Human) Friedreich ataxia Caution: Indicated by Coriell to have 420 and 541 GAA repeats., Population: Caucasian. Transformed cell line Male CLO:CLO_0016225,
Coriell:GM04079,
Wikidata:Q54838383
CVCL_T821 Cellosaurus 2026-09-26 06:49:13 0
GM03928
 
Resource Report
Resource Website
RRID:CVCL_N013 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18013 CLO:CLO_0016014,
CLO:CLO_0016138,
Coriell:GM03928,
Coriell:GM18013,
Wikidata:Q54838328
CVCL_N013 Cellosaurus 2026-09-26 06:49:12 0
GM03928
 
Resource Report
Resource Website
Coriell Cat# GM18013, RRID:CVCL_N013 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18013 Coriell GM18013 CLO:CLO_0016014,
CLO:CLO_0016138,
Coriell:GM03928,
Coriell:GM18013,
Wikidata:Q54838328
CVCL_N013 Cellosaurus 2026-09-26 06:49:12 0
GM03998
 
Resource Report
Resource Website
RRID:CVCL_IZ39 Homo sapiens (Human) Hyperlipoproteinemia, type I Population: Caucasian. Finite cell line Male CLO:CLO_0016074,
Coriell:GM03998,
Wikidata:Q54838364
CVCL_IZ39 Cellosaurus 2026-09-26 06:49:13 0
GM03940
 
Resource Report
Resource Website
RRID:CVCL_CY31 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Finite cell line Male CLO:CLO_0016105,
Coriell:GM03940,
Wikidata:Q54838334
CVCL_CY31 Cellosaurus 2026-09-26 06:49:12 0
GM03944
 
Resource Report
Resource Website
RRID:CVCL_CY35 Homo sapiens (Human) Familial adenomatous polyposis Population: Caucasian. Finite cell line Female CLO:CLO_0016109,
Coriell:GM03944,
Wikidata:Q54838339
CVCL_CY35 Cellosaurus 2026-09-26 06:49:12 0
GM04025
 
Resource Report
Resource Website
RRID:CVCL_1N28 Homo sapiens (Human) Fragile X syndrome Population: African American. PMID:1672039
PMID:25776194
PMID:33426406
Transformed cell line Male GM4025B, GM04025C, GM04025E CLO:CLO_0016229,
Coriell:GM04025,
Wikidata:Q54838374
CVCL_1N28 Cellosaurus 2026-09-26 06:49:13 0
GM03941
 
Resource Report
Resource Website
Coriell Cat# GM03941, RRID:CVCL_CY32 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Transformed cell line Male GM03941B Coriell GM03941 CLO:CLO_0016108,
Coriell:GM03941,
Wikidata:Q54838336
CVCL_CY32 Cellosaurus 2026-09-26 06:49:12 0
GM03918
 
Resource Report
Resource Website
RRID:CVCL_X115 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM 3918 CLO:CLO_0016128,
Coriell:GM03918,
Wikidata:Q54838326
CVCL_X115 Cellosaurus 2026-09-26 06:49:12 0
GM04127
 
Resource Report
Resource Website
Coriell Cat# GM04127, RRID:CVCL_X303 Homo sapiens (Human) Population: African American. PMID:6661932
PMID:23665875
Finite cell line Female GM 4127 Coriell GM04127 CLO:CLO_0016194,
Coriell:GM04127,
Wikidata:Q54838393
CVCL_X303 Cellosaurus 2026-09-26 06:49:13 0
GM04088
 
Resource Report
Resource Website
Coriell Cat# GM04088, RRID:CVCL_2T00 Homo sapiens (Human) Karyotypic information: 46,XX,t(1;4)(1pter->1q32::4p16->4pter;4qter->4p16::1q32->1qter) (Coriell=GM04088)., Population: Caucasian. Finite cell line Female Coriell GM04088 CLO:CLO_0016221,
Coriell:GM04088,
Wikidata:Q54838385
CVCL_2T00 Cellosaurus 2026-09-26 06:49:13 0
GM04012
 
Resource Report
Resource Website
Coriell Cat# GM04012, RRID:CVCL_2S99 Homo sapiens (Human) Karyotypic information: 46,XX,t(2;5)(2qter->2p25::5q33->5qter;5pter->5q33::2p25->2pter) (Coriell=GM04012)., Population: Caucasian. Finite cell line Female Coriell GM04012 CLO:CLO_0016069,
Coriell:GM04012,
Wikidata:Q54838366
CVCL_2S99 Cellosaurus 2026-09-26 06:49:13 0
GM03929
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5M87 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:6726265
PMID:7253718
PMID:21354051
PMID:23665875
Transformed cell line Male GM03929A, AG03929, AG 3929, AG3929 CLO:CLO_0016136,
Coriell:AG03929,
Coriell:GM03929,
Wikidata:Q54838329
CVCL_5M87 Cellosaurus 2026-09-26 06:49:12 0
GM03932
 
Resource Report
Resource Website
Coriell Cat# GM03932, RRID:CVCL_9S53 Homo sapiens (Human) Limb-girdle muscular dystrophy type 2A Population: Caucasian. Finite cell line Male Coriell GM03932 CLO:CLO_0016132,
Coriell:GM03932,
Wikidata:Q54838331
CVCL_9S53 Cellosaurus 2026-09-26 06:49:12 0
GM03935
 
Resource Report
Resource Website
RRID:CVCL_X301 Homo sapiens (Human) Isodicentric chromosome Karyotypic information: 46,X,i(X)(q26) (PubMed=10377420)., Population: Caucasian. PMID:6661932
PMID:10377420
Finite cell line Female GM 3935 CLO:CLO_0016104,
Coriell:GM03935,
Wikidata:Q54838333
CVCL_X301 Cellosaurus 2026-09-26 06:49:12 0
GM03952
 
Resource Report
Resource Website
Coriell Cat# GM03952, RRID:CVCL_CY41 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Finite cell line Female Coriell GM03952 CLO:CLO_0016096,
Coriell:GM03952,
Wikidata:Q54838347
CVCL_CY41 Cellosaurus 2026-09-26 06:49:12 0
GM04034
 
Resource Report
Resource Website
RRID:CVCL_F112 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. PMID:23680132 Transformed cell line Male CLO:CLO_0016232,
Coriell:GM04034,
Wikidata:Q54838377
CVCL_F112 Cellosaurus 2026-09-26 06:49:13 0
GM03941
 
Resource Report
Resource Website
RRID:CVCL_CY32 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Transformed cell line Male GM03941B CLO:CLO_0016108,
Coriell:GM03941,
Wikidata:Q54838336
CVCL_CY32 Cellosaurus 2026-09-26 06:49:12 0

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