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236,573 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
GM03237
 
Resource Report
Resource Website
Coriell Cat# GM18010, RRID:CVCL_F072 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:7438795 Transformed cell line Male GM3237, GM18010 Coriell GM18010 CLO:CLO_0016000,
CLO:CLO_0016730,
BioSample:SAMN00808316,
Coriell:GM03237,
Coriell:GM18010,
Wikidata:Q54837958
CVCL_F072 2026-09-12 05:32:25 0
GM03213
 
Resource Report
Resource Website
RRID:CVCL_HQ57 Homo sapiens (Human) Idiopathic torsion dystonia Population: Caucasian. Finite cell line Female CLO:CLO_0013377,
BioSample:SAMN00808298,
Coriell:GM03213,
Wikidata:Q54837940
CVCL_HQ57 2026-09-12 05:32:24 0
GM03216
 
Resource Report
Resource Website
RRID:CVCL_HQ60 Homo sapiens (Human) Idiopathic torsion dystonia Population: Caucasian. Finite cell line Female CLO:CLO_0013374,
BioSample:SAMN00808301,
Coriell:GM03216,
Wikidata:Q54837943
CVCL_HQ60 2026-09-12 05:32:24 0
GM03130
 
Resource Report
Resource Website
Coriell Cat# GM03130, RRID:CVCL_JM09 Homo sapiens (Human) Anetoderma Finite cell line Female Coriell GM03130 CLO:CLO_0013575,
BioSample:SAMN00808263,
Coriell:GM03130,
Wikidata:Q54837892
CVCL_JM09 2026-09-12 05:32:23 0
GM03222
 
Resource Report
Resource Website
RRID:CVCL_HQ64 Homo sapiens (Human) Idiopathic torsion dystonia Population: Jewish; Ashkenazi. Finite cell line Female CLO:CLO_0016473,
BioSample:SAMN00808307,
Coriell:GM03222,
Wikidata:Q54837949
CVCL_HQ64 2026-09-12 05:32:24 0
GM03236
 
Resource Report
Resource Website
RRID:CVCL_X440 Homo sapiens (Human) Type 1 diabetes mellitus Population: Caucasian. PMID:7438795 Transformed cell line Male GM3236 CLO:CLO_0016732,
BioSample:SAMN00808315,
Coriell:GM03236,
Wikidata:Q54837957
CVCL_X440 2026-09-12 05:32:24 0
GM03195
 
Resource Report
Resource Website
RRID:CVCL_AB31 Homo sapiens (Human) Dyskeratosis congenita Transformed cell line Male CLO:CLO_0013397,
BioSample:SAMN00808288,
Coriell:GM03195,
Wikidata:Q54837930
CVCL_AB31 2026-09-12 05:32:24 0
GM03200
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM03200, RRID:CVCL_AX76 Homo sapiens (Human) Fragile X syndrome PMID:1672039 Transformed cell line Male GM3200 Coriell GM03200 CLO:CLO_0013391,
BioSample:SAMN00808291,
Coriell:GM03200,
Wikidata:Q54837933
CVCL_AX76 2026-09-12 05:32:24 2
GM03191
 
Resource Report
Resource Website
Coriell Cat# GM03191, RRID:CVCL_EJ32 Homo sapiens (Human) Population: Caucasian. Finite cell line Male Coriell GM03191 CLO:CLO_0013428,
BioSample:SAMN00808284,
Coriell:GM03191,
Wikidata:Q54837926
CVCL_EJ32 2026-09-12 05:32:23 0
GM03218
 
Resource Report
Resource Website
Coriell Cat# GM03218, RRID:CVCL_4N42 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Population: Caucasian. Finite cell line Male Coriell GM03218 CLO:CLO_0013382,
BioSample:SAMN00808303,
Coriell:GM03218,
Wikidata:Q54837945
CVCL_4N42 2026-09-12 05:32:24 0
GM03226
 
Resource Report
Resource Website
RRID:CVCL_M938 Homo sapiens (Human) Trisomy 9 Population: Caribbean; Trinidadian., Part of: Human variation panel. PMID:6661932
PMID:23665875
Finite cell line Male GM 3226, GM17354 CLO:CLO_0013718,
CLO:CLO_0016469,
BioSample:SAMN00808311,
Coriell:GM03226,
Coriell:GM17354,
Wikidata:Q54837953
CVCL_M938 2026-09-12 05:32:24 0
GM03238
 
Resource Report
Resource Website
Coriell Cat# GM03238, RRID:CVCL_F074 Homo sapiens (Human) Population: Caucasian. PMID:7438795 Transformed cell line Female GM3238, GM03238B Coriell GM03238 CLO:CLO_0016733,
BioSample:SAMN00808317,
Coriell:GM03238,
Wikidata:Q54837959
CVCL_F074 2026-09-12 05:32:25 0
GM03138
 
Resource Report
Resource Website
Coriell Cat# GM03138, RRID:CVCL_DD74 Homo sapiens (Human) Osteogenesis imperfecta Population: Caucasian. Finite cell line Female Coriell GM03138 CLO:CLO_0013524,
BioSample:SAMN00808267,
Coriell:GM03138,
Wikidata:Q54837898
CVCL_DD74 2026-09-12 05:32:23 0
GM03223
 
Resource Report
Resource Website
RRID:CVCL_CY29 Homo sapiens (Human) Familial adenomatous polyposis Population: Caucasian. Finite cell line Male CLO:CLO_0016476,
BioSample:SAMN00808308,
Coriell:GM03223,
Wikidata:Q54837950
CVCL_CY29 2026-09-12 05:32:24 0
GM03225
 
Resource Report
Resource Website
RRID:CVCL_X139 Homo sapiens (Human) Trisomy 9 Population: Caribbean; Trinidadian. PMID:6661932
PMID:23665875
Finite cell line Female GM 3225, GM03225A CLO:CLO_0016470,
BioSample:SAMN00808310,
Coriell:GM03225,
Wikidata:Q54837952
CVCL_X139 2026-09-12 05:32:24 0
GM03210
 
Resource Report
Resource Website
RRID:CVCL_HQ56 Homo sapiens (Human) Idiopathic torsion dystonia Population: Caucasian. Finite cell line Male CLO:CLO_0013369,
BioSample:SAMN00808296,
Coriell:GM03210,
Wikidata:Q54837938
CVCL_HQ56 2026-09-12 05:32:24 0
GM03235
 
Resource Report
Resource Website
RRID:CVCL_X441 Homo sapiens (Human) Type 1 diabetes mellitus Population: Caucasian. PMID:7438795 Transformed cell line Male GM3235 CLO:CLO_0016477,
BioSample:SAMN00808314,
Coriell:GM03235,
Wikidata:Q54837956
CVCL_X441 2026-09-12 05:32:24 0
GM03192
 
Resource Report
Resource Website
RRID:CVCL_EJ33 Homo sapiens (Human) Population: Caucasian; Irish/Scottish. Finite cell line Female CLO:CLO_0013389,
BioSample:SAMN00808285,
Coriell:GM03192,
Wikidata:Q54837927
CVCL_EJ33 2026-09-12 05:32:23 0
GM03220
 
Resource Report
Resource Website
RRID:CVCL_HQ63 Homo sapiens (Human) Idiopathic torsion dystonia Population: Caucasian. Finite cell line Male CLO:CLO_0016478,
BioSample:SAMN00808305,
Coriell:GM03220,
Wikidata:Q54837947
CVCL_HQ63 2026-09-12 05:32:24 0
GM03241
 
Resource Report
Resource Website
Coriell Cat# GM03241, RRID:CVCL_X281 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 3241, GM03241A Coriell GM03241 CLO:CLO_0016738,
BioSample:SAMN00808320,
Coriell:GM03241,
Wikidata:Q54837962
CVCL_X281 2026-09-12 05:32:25 0

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