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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
GM07537
 
Resource Report
Resource Website
RRID:CVCL_AY17 Homo sapiens (Human) PMID:25776194 Transformed cell line Female GM07537A CLO:CLO_0016433,
Coriell:GM07537,
Wikidata:Q54842835
CVCL_AY17 2026-09-12 05:33:23 0
GM07535
 
Resource Report
Resource Website
RRID:CVCL_7472 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Male GM17276 CLO:CLO_0013199,
CLO:CLO_0016431,
Coriell:GM07535,
Coriell:GM17276,
GEO:GSM569732,
GEO:GSM596340,
GEO:GSM596762,
GEO:GSM924878,
Wikidata:Q54842833
CVCL_7472 2026-09-12 05:33:22 0
GM07524
 
Resource Report
Resource Website
RRID:CVCL_7469 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Female GM17275 CLO:CLO_0013202,
CLO:CLO_0016441,
Coriell:GM07524,
Coriell:GM17275,
GEO:GSM569731,
GEO:GSM596339,
GEO:GSM596761,
GEO:GSM924877,
Wikidata:Q54842824
CVCL_7469 2026-09-12 05:33:22 0
GM07482
 
Resource Report
Resource Website
Coriell Cat# GM07482, RRID:CVCL_AL17 Homo sapiens (Human) Retinitis pigmentosa Population: Jewish. Transformed cell line Male Coriell GM07482 CLO:CLO_0016485,
Coriell:GM07482,
Wikidata:Q54842783
CVCL_AL17 2026-09-12 05:33:21 0
GM07540
 
Resource Report
Resource Website
RRID:CVCL_AY20 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0016436,
Coriell:GM07540,
Wikidata:Q54842838
CVCL_AY20 2026-09-12 05:33:23 0
GM07674
 
Resource Report
Resource Website
RRID:CVCL_0M69 Homo sapiens (Human) Population: Caucasian. Transformed cell line Male CLO:CLO_0016372,
Coriell:GM07674,
Wikidata:Q54842860
CVCL_0M69 2026-09-12 05:33:23 0
GM07730
 
Resource Report
Resource Website
RRID:CVCL_AY24 Homo sapiens (Human) Fragile X syndrome Population: Caucasian. Finite cell line Male GM07730A CLO:CLO_0016399,
Coriell:GM07730,
Wikidata:Q54842876
CVCL_AY24 2026-09-12 05:33:23 0
GM07544
 
Resource Report
Resource Website
Coriell Cat# GM17277, RRID:CVCL_7473 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Female GM 07544, GM17277 Coriell GM17277 CLO:CLO_0013208,
CLO:CLO_0016387,
Coriell:GM07544,
Coriell:GM17277,
GEO:GSM569755,
GEO:GSM596341,
GEO:GSM596811,
GEO:GSM924879,
Wikidata:Q54842847
CVCL_7473 2026-09-12 05:33:23 0
GM07778
 
Resource Report
Resource Website
RRID:CVCL_4H13 Homo sapiens (Human) Bipolar disorder Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male GM07778C CLO:CLO_0016355,
Coriell:GM07778,
Wikidata:Q54842903
CVCL_4H13 2026-09-12 05:33:24 0
GM07678
 
Resource Report
Resource Website
Coriell Cat# GM07678, RRID:CVCL_5B81 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:17668376
PMID:20856902
Transformed cell line Male GM07678A, CEPH-1333-NA07678, 1333-8277 Coriell GM07678 CLO:CLO_0016374,
Coriell:GM07678,
dbMHC:48580,
GEO:GSM25428,
GEO:GSM316486,
GEO:GSM316487,
GEO:GSM316488,
GEO:GSM420591,
IHW:IHW01041,
IPD-IMGT/HLA:25841,
Wikidata:Q54842863
CVCL_5B81 2026-09-12 05:33:23 0
GM07743
 
Resource Report
Resource Website
RRID:CVCL_9X05 Homo sapiens (Human) Population: Japanese. Transformed cell line Female CLO:CLO_0016394,
Coriell:GM07743,
Wikidata:Q54842883
CVCL_9X05 2026-09-12 05:33:24 0
GM07726
 
Resource Report
Resource Website
RRID:CVCL_V049 Homo sapiens (Human) Marfan syndrome Population: African American. Finite cell line Female CLO:CLO_0016405,
Coriell:GM07726,
Wikidata:Q54842874
CVCL_V049 2026-09-12 05:33:23 0
GM07675
 
Resource Report
Resource Website
Coriell Cat# GM07675, RRID:CVCL_9R29 Homo sapiens (Human) Adrenoleukodystrophy Population: Hispanic. Finite cell line Male Coriell GM07675 CLO:CLO_0016371,
Coriell:GM07675,
Wikidata:Q54842861
CVCL_9R29 2026-09-12 05:33:23 0
GM07712
 
Resource Report
Resource Website
Coriell Cat# GM18028, RRID:CVCL_N071 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18028 Coriell GM18028 CLO:CLO_0015595,
CLO:CLO_0016407,
Coriell:GM07712,
Coriell:GM18028,
Wikidata:Q54842872
CVCL_N071 2026-09-12 05:33:23 0
GM07773
 
Resource Report
Resource Website
RRID:CVCL_5N69 Homo sapiens (Human) Chronic granulomatous disease PMID:23665875 Transformed cell line Female CLO:CLO_0016358,
Coriell:GM07773,
Wikidata:Q54842898
CVCL_5N69 2026-09-12 05:33:24 0
GM07551
 
Resource Report
Resource Website
RRID:CVCL_EJ53 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM07551A CLO:CLO_0016381,
Coriell:GM07551,
Wikidata:Q54842853
CVCL_EJ53 2026-09-12 05:33:23 0
GM07779
 
Resource Report
Resource Website
Coriell Cat# GM07779, RRID:CVCL_4H14 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female GM07779C Coriell GM07779 CLO:CLO_0010201,
Coriell:GM07779,
Wikidata:Q54842904
CVCL_4H14 2026-09-12 05:33:24 0
GM07553
 
Resource Report
Resource Website
RRID:CVCL_0M66 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0016379,
Coriell:GM07553,
Wikidata:Q54842855
CVCL_0M66 2026-09-12 05:33:23 0
GM07547
 
Resource Report
Resource Website
Coriell Cat# GM07547, RRID:CVCL_AW88 Homo sapiens (Human) Transformed cell line Female Coriell GM07547 CLO:CLO_0016384,
Coriell:GM07547,
Wikidata:Q54842850
CVCL_AW88 2026-09-12 05:33:23 0
GM07731
 
Resource Report
Resource Website
Coriell Cat# GM07731, RRID:CVCL_0M70 Homo sapiens (Human) Transformed cell line Female GM07731A Coriell GM07731 CLO:CLO_0016397,
Coriell:GM07731,
Wikidata:Q54842877
CVCL_0M70 2026-09-12 05:33:23 0

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