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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
GM05118
 
Resource Report
Resource Website
RRID:CVCL_5N14 Homo sapiens (Human) Population: Caucasian. Finite cell line Male CLO:CLO_0025373,
Coriell:GM05118,
Wikidata:Q54838868
CVCL_5N14 2026-08-08 05:00:24 0
GM05131
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_AX78 Homo sapiens (Human) Fragile X syndrome Population: Caucasian. Finite cell line Male CLO:CLO_0025352,
Coriell:GM05131,
Wikidata:Q54838877
CVCL_AX78 2026-08-08 05:00:23 1
GM05107
 
Resource Report
Resource Website
RRID:CVCL_AA54 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Male CLO:CLO_0025316,
Coriell:GM05107,
Wikidata:Q54838855
CVCL_AA54 2026-08-08 05:00:24 0
GM05168
 
Resource Report
Resource Website
RRID:CVCL_1K29 Homo sapiens (Human) Charcot-Marie-Tooth disease type 1A Population: Caucasian. Transformed cell line Female CLO:CLO_0025264,
Coriell:GM05168,
Wikidata:Q54838903
CVCL_1K29 2026-08-08 05:00:25 0
GM05168
 
Resource Report
Resource Website
Coriell Cat# GM05168, RRID:CVCL_1K29 Homo sapiens (Human) Charcot-Marie-Tooth disease type 1A Population: Caucasian. Transformed cell line Female Coriell GM05168 CLO:CLO_0025264,
Coriell:GM05168,
Wikidata:Q54838903
CVCL_1K29 2026-08-08 05:00:23 0
GM05131
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM05131, RRID:CVCL_AX78 Homo sapiens (Human) Fragile X syndrome Population: Caucasian. Finite cell line Male Coriell GM05131 CLO:CLO_0025352,
Coriell:GM05131,
Wikidata:Q54838877
CVCL_AX78 2026-08-08 05:00:23 1
GM05135
 
Resource Report
Resource Website
Coriell Cat# GM05135, RRID:CVCL_GQ39 Homo sapiens (Human) Bipolar disorder Population: Caucasian; Irish. Transformed cell line Female GM05135A Coriell GM05135 CLO:CLO_0025349,
Coriell:GM05135,
Wikidata:Q54838882
CVCL_GQ39 2026-08-08 05:00:23 0
GM05149
 
Resource Report
Resource Website
RRID:CVCL_1K25 Homo sapiens (Human) Charcot-Marie-Tooth disease type 1A Population: Caucasian. Transformed cell line Male CLO:CLO_0025242,
Coriell:GM05149,
Wikidata:Q54838888
CVCL_1K25 2026-08-08 05:00:23 0
GM05082
 
Resource Report
Resource Website
RRID:CVCL_U481 Homo sapiens (Human) Becker's muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Transformed cell line Male CLO:CLO_0025338,
Coriell:GM05082,
Wikidata:Q54838845
CVCL_U481 2026-08-08 05:00:22 0
GM05134
 
Resource Report
Resource Website
RRID:CVCL_GQ38 Homo sapiens (Human) Bipolar disorder Population: Caucasian; Irish. Transformed cell line Male CLO:CLO_0025351,
Coriell:GM05134,
Wikidata:Q54838881
CVCL_GQ38 2026-08-08 05:00:23 0
GM05161
 
Resource Report
Resource Website
RRID:CVCL_F292 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:16260726 Transformed cell line Male GM05161A, GM17223 CLO:CLO_0014367,
CLO:CLO_0025255,
Coriell:GM05161,
Coriell:GM17223,
GEO:GSM569603,
GEO:GSM596287,
GEO:GSM596647,
GEO:GSM924825,
Wikidata:Q54838896
CVCL_F292 2026-08-08 05:00:24 0
GM05161
 
Resource Report
Resource Website
Coriell Cat# GM17223, RRID:CVCL_F292 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:16260726 Transformed cell line Male GM05161A, GM17223 Coriell GM17223 CLO:CLO_0014367,
CLO:CLO_0025255,
Coriell:GM05161,
Coriell:GM17223,
GEO:GSM569603,
GEO:GSM596287,
GEO:GSM596647,
GEO:GSM924825,
Wikidata:Q54838896
CVCL_F292 2026-08-08 05:00:23 0
GM05151
 
Resource Report
Resource Website
RRID:CVCL_AW58 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. Finite cell line Male CLO:CLO_0025245,
Coriell:GM05151,
Wikidata:Q54838889
CVCL_AW58 2026-08-08 05:00:23 0
GM05119
 
Resource Report
Resource Website
RRID:CVCL_5N15 Homo sapiens (Human) Population: Caucasian. Transformed cell line Male CLO:CLO_0025371,
Coriell:GM05119,
Wikidata:Q54838869
CVCL_5N15 2026-08-08 05:00:23 0
GM05132
 
Resource Report
Resource Website
Coriell Cat# GM05132, RRID:CVCL_AX79 Homo sapiens (Human) Finite cell line Female Coriell GM05132 CLO:CLO_0025355,
Coriell:GM05132,
Wikidata:Q54838878
CVCL_AX79 2026-08-08 05:00:23 0
GM05164
 
Resource Report
Resource Website
RRID:CVCL_AW61 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:23680132 Transformed cell line Female CLO:CLO_0025254,
Coriell:GM05164,
Wikidata:Q54838899
CVCL_AW61 2026-08-08 05:00:23 0
GM05126
 
Resource Report
Resource Website
RRID:CVCL_5N19 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian. PMID:6726265
PMID:23665875
Transformed cell line Male RB 5126 CLO:CLO_0025359,
Coriell:GM05126,
Wikidata:Q54838874
CVCL_5N19 2026-08-08 05:00:23 0
GM05156
 
Resource Report
Resource Website
RRID:CVCL_4F91 Homo sapiens (Human) Bipolar disorder Population: Caucasian. Transformed cell line Female GM5156, GM05156A CLO:CLO_0025247,
Coriell:GM05156,
Wikidata:Q54838891
CVCL_4F91 2026-08-08 05:00:23 0
GM05087
 
Resource Report
Resource Website
Coriell Cat# GM05087, RRID:CVCL_5N05 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell GM05087 CLO:CLO_0025336,
Coriell:GM05087,
Wikidata:Q54838846
CVCL_5N05 2026-08-08 05:00:23 0
GM05162
 
Resource Report
Resource Website
RRID:CVCL_5N26 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian. Finite cell line Male CLO:CLO_0025256,
Coriell:GM05162,
Wikidata:Q54838897
CVCL_5N26 2026-08-08 05:00:24 0

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