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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
GM01848
 
Resource Report
Resource Website
RRID:CVCL_X257 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM-1848, GM 1848 CLO:CLO_0031428,
BioSample:SAMN00807219,
Coriell:GM01848,
Wikidata:Q54837122
CVCL_X257 2026-07-25 04:32:26 0
GM01840
 
Resource Report
Resource Website
Possibly Discontinued
Possibly Discontinued
Possibly Discontinued
Coriell Cat# GM01840, RRID:CVCL_M987 Homo sapiens (Human) Population: South American (Brazil, Guyana, Venezuela)., Part of: Human variation panel. PMID:7253718
PMID:23665875
Finite cell line Female GM-1840, GM17311, AG01840, AG-1840, AG 1840, AG1840 Coriell GM01840 CLO:CLO_0013354,
CLO:CLO_0031415,
BioSample:SAMN00807217,
Coriell:AG01840,
Coriell:GM01840,
Coriell:GM17311,
Wikidata:Q54837116
CVCL_M987 2026-07-25 04:32:26 0
GM01841
 
Resource Report
Resource Website
RRID:CVCL_1L43 Homo sapiens (Human) Ataxia telangiectasia syndrome Finite cell line Male GM-1841, GM01841A CLO:CLO_0031427,
Coriell:GM01841,
Wikidata:Q54837117
CVCL_1L43 2026-07-25 04:32:24 0
GM01870
 
Resource Report
Resource Website
RRID:CVCL_4J39 Homo sapiens (Human) Glucose-6-phosphate dehydrogenase deficiency Population: Caucasian. PMID:7803800 Finite cell line Male GM-1870 CLO:CLO_0032403,
BioSample:SAMN00807248,
Coriell:GM01870,
Wikidata:Q54837145
CVCL_4J39 2026-07-25 04:32:25 0
GM01893
 
Resource Report
Resource Website
Coriell Cat# GM01893, RRID:CVCL_F016 Homo sapiens (Human) Intellectual developmental disorder Karyotypic information: 46,XY,del(9)(pter->q11::q21.3->qter) (Coriell=GM01893). PMID:6617268
PMID:6661932
Finite cell line Male GM-1893, GM 1893 Coriell GM01893 CLO:CLO_0032428,
Coriell:GM01893,
Wikidata:Q54837166
CVCL_F016 2026-07-25 04:32:26 0
GM01879
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_DF18 Homo sapiens (Human) Retinoblastoma PMID:7253718
PMID:7471105
Finite cell line Female GM-1879, GM01879A, AG01879, AG-1879, AG 1879, AG1879 CLO:CLO_0032408,
BioSample:SAMN00807268,
Coriell:AG01879,
Coriell:GM01879,
Wikidata:Q54837154
CVCL_DF18 2026-07-25 04:32:25 0
GM01873
 
Resource Report
Resource Website
Coriell Cat# GM01873, RRID:CVCL_GR93 Homo sapiens (Human) Type 1 diabetes mellitus Population: Caucasian. Finite cell line Female GM-1873, GM1873 Coriell GM01873 CLO:CLO_0032400,
BioSample:SAMN00807254,
Coriell:GM01873,
Wikidata:Q54837148
CVCL_GR93 2026-07-25 04:32:26 0
GM01860
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01860, RRID:CVCL_JC74 Homo sapiens (Human) Neurofibromatosis type 1 Population: Caucasian. Finite cell line Male GM-1860 Coriell GM01860 Coriell:GM01860,
Wikidata:Q54837133
CVCL_JC74 2026-07-25 04:32:26 0
GM01876
 
Resource Report
Resource Website
RRID:CVCL_CY04 Homo sapiens (Human) Population: Caucasian. PMID:7438795 Finite cell line Male GM-1876, GM1876 CLO:CLO_0032401,
BioSample:SAMN00807260,
Coriell:GM01876,
Wikidata:Q54837151
CVCL_CY04 2026-07-25 04:32:25 0
GM01861
 
Resource Report
Resource Website
RRID:CVCL_9Z60 Homo sapiens (Human) Neurofibromatosis type 1 Population: Caucasian. Transformed cell line Male GM-1861, GM01861A CLO:CLO_0031397,
BioSample:SAMN00807238,
Coriell:GM01861,
Wikidata:Q54837134
CVCL_9Z60 2026-07-25 04:32:25 0
GM01877
 
Resource Report
Resource Website
Coriell Cat# GM01877, RRID:CVCL_F076 Homo sapiens (Human) Population: Caucasian. PMID:7438795
PMID:24555846
Finite cell line Male GM-1877, GM1877 Coriell GM01877 CLO:CLO_0032407,
BioSample:SAMN00807264,
Coriell:GM01877,
GEO:GSM1288434,
Wikidata:Q54837152
CVCL_F076 2026-07-25 04:32:25 0
GM01893
 
Resource Report
Resource Website
RRID:CVCL_F016 Homo sapiens (Human) Intellectual developmental disorder Karyotypic information: 46,XY,del(9)(pter->q11::q21.3->qter) (Coriell=GM01893). PMID:6617268
PMID:6661932
Finite cell line Male GM-1893, GM 1893 CLO:CLO_0032428,
Coriell:GM01893,
Wikidata:Q54837166
CVCL_F016 2026-07-25 04:32:26 0
GM01981
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_F589 Homo sapiens (Human) Menkes disease Population: Caucasian. PMID:7438975
PMID:7977350
Finite cell line Male GM-1981, GM1981 CLO:CLO_0032339,
BioSample:SAMN00807346,
Coriell:GM01981,
Wikidata:Q54837212
CVCL_F589 2026-07-25 04:32:27 1
GM02007
 
Resource Report
Resource Website
Coriell Cat# GM02007, RRID:CVCL_AM83 Homo sapiens (Human) Ehlers-Danlos syndrome, type I Population: Caucasian. Finite cell line Female GM-2007 Coriell GM02007 CLO:CLO_0032297,
BioSample:SAMN00807376,
Coriell:GM02007,
Wikidata:Q54837232
CVCL_AM83 2026-07-25 04:32:27 0
GM01918
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD80 Homo sapiens (Human) Finite cell line Male GM-1918 Coriell:GM01918,
Wikidata:Q54837184
CVCL_JD80 2026-07-25 04:32:26 0
GM01953
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01953, RRID:CVCL_7344 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:7519740
PMID:7664335
PMID:8483505
PMID:9025096
PMID:14583597
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Female GM-1953, GM1953, GM01953A, GM01079, GM-1079, GM17216 Coriell GM01953 CLO:CLO_0013888,
CLO:CLO_0032336,
BioSample:SAMN00807332,
Coriell:GM01079,
Coriell:GM01953,
Coriell:GM17216,
GEO:GSM569530,
GEO:GSM596280,
GEO:GSM596640,
GEO:GSM924818,
Wikidata:Q54837200
CVCL_7344 2026-07-25 04:32:26 0
GM01995
 
Resource Report
Resource Website
Coriell Cat# GM01995, RRID:CVCL_AK20 Homo sapiens (Human) Sitosterolemia Population: Caucasian. Finite cell line Male GM-1995 Coriell GM01995 CLO:CLO_0032281,
BioSample:SAMN00807360,
Coriell:GM01995,
Wikidata:Q54837220
CVCL_AK20 2026-07-25 04:32:28 0
GM02000
 
Resource Report
Resource Website
RRID:CVCL_1V08 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Population: Caucasian. PMID:6089204
PMID:6986448
PMID:29308438
Finite cell line Female GM-2000, GM 2000, GM2000, GM02000F CLO:CLO_0032294,
BioSample:SAMN00807370,
Coriell:GM02000,
Wikidata:Q54837228
CVCL_1V08 2026-07-25 04:32:27 0
GM01938
 
Resource Report
Resource Website
RRID:CVCL_AD64 Homo sapiens (Human) Maple syrup urine disease Population: Caucasian. Finite cell line Male GM1938, GM-1938 CLO:CLO_0032325,
BioSample:SAMN00807326,
Coriell:GM01938,
Wikidata:Q54837197
CVCL_AD64 2026-07-25 04:32:27 0
GM01919
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01919, RRID:CVCL_JE14 Homo sapiens (Human) Transformed cell line Male GM-1919 Coriell GM01919 Coriell:GM01919,
Wikidata:Q54837185
CVCL_JE14 2026-07-25 04:32:26 0

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