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95,747 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
GM03540
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UT35 Homo sapiens (Human) Gyrate atrophy Transformed cell line Female Coriell:GM03540,
Wikidata:Q93584685
CVCL_UT35 2026-07-25 04:32:48 0
GM03552
 
Resource Report
Resource Website
Coriell Cat# GM17083, RRID:CVCL_N009 Homo sapiens (Human) Karyotypic information: 46,X,t(X;11)(q26;q23) (PubMed=10377420)., Population: Southeast Asian; Vietnamese., Part of: Human variation panel. PMID:2498246
PMID:6947233
PMID:10377420
Finite cell line Female GM3552, GM 3552, GM03552A, GM3552A, GM17083 Coriell GM17083 CLO:CLO_0014480,
CLO:CLO_0017271,
BioSample:SAMN00808447,
Coriell:GM03552,
Coriell:GM17083,
Wikidata:Q54838125
CVCL_N009 2026-07-25 04:32:48 0
GM03640
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# AG03640, RRID:CVCL_DF20 Homo sapiens (Human) Retinoblastoma PMID:7253718 Transformed cell line Female AG03640, AG3640 Coriell AG03640 CLO:CLO_0017161,
BioSample:SAMN00808477,
Coriell:AG03640,
Coriell:GM03640,
Wikidata:Q54838169
CVCL_DF20 2026-07-25 04:32:49 0
GM03638
 
Resource Report
Resource Website
Coriell Cat# GM03638, RRID:CVCL_F187 Homo sapiens (Human) PMID:62390
PMID:8547074
Transformed cell line Female GM 3638, GM03638B, GM03638C, B cell line 8392, 8392 Coriell GM03638 CLO:CLO_0017157,
Coriell:GM03638,
Cosmic:2361360,
Wikidata:Q54838167
CVCL_F187 2026-07-25 04:32:49 0
GM03721
 
Resource Report
Resource Website
Coriell Cat# GM17157, RRID:CVCL_M941 Homo sapiens (Human) Population: African American., Part of: Human variation panel. Transformed cell line Female GM17157 Coriell GM17157 CLO:CLO_0013962,
CLO:CLO_0015467,
BioSample:SAMN00808507,
Coriell:GM03721,
Coriell:GM17157,
GEO:GSM273424,
GEO:GSM569659,
GEO:GSM596222,
GEO:GSM597022,
GEO:GSM924667,
Wikidata:Q54838206
CVCL_M941 2026-07-25 04:32:50 0
GM03696
 
Resource Report
Resource Website
RRID:CVCL_M944 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:23680132 Transformed cell line Female GM03696B, GM03696C CLO:CLO_0015480,
BioSample:SAMN00808499,
Coriell:GM03696,
Wikidata:Q54838194
CVCL_M944 2026-07-25 04:32:50 0
GM03614
 
Resource Report
Resource Website
RRID:CVCL_1F15 Homo sapiens (Human) Xeroderma pigmentosum Finite cell line Female GM 3614 CLO:CLO_0017189,
BioSample:SAMN00808470,
Coriell:GM03614,
Wikidata:Q54838157
CVCL_1F15 2026-07-25 04:32:49 0
GM03720
 
Resource Report
Resource Website
RRID:CVCL_M940 Homo sapiens (Human) Population: African American. Finite cell line Female CLO:CLO_0015462,
BioSample:SAMN00808506,
Coriell:GM03720,
Wikidata:Q54838205
CVCL_M940 2026-07-25 04:32:50 0
GM03720
 
Resource Report
Resource Website
Coriell Cat# GM03720, RRID:CVCL_M940 Homo sapiens (Human) Population: African American. Finite cell line Female Coriell GM03720 CLO:CLO_0015462,
BioSample:SAMN00808506,
Coriell:GM03720,
Wikidata:Q54838205
CVCL_M940 2026-07-25 04:32:50 0
GM03623
 
Resource Report
Resource Website
Coriell Cat# GM03623, RRID:CVCL_X295 Homo sapiens (Human) Trisomy 18 Population: African American. PMID:6661932
PMID:23665875
Finite cell line Female GM 3623 Coriell GM03623 CLO:CLO_0017193,
BioSample:SAMN00808473,
Coriell:GM03623,
Wikidata:Q54838163
CVCL_X295 2026-07-25 04:32:49 0
GM03715
 
Resource Report
Resource Website
Coriell Cat# GM17001, RRID:CVCL_7401 Homo sapiens (Human) Population: Caucasian; Northern European., Part of: Human variation panel. PMID:11416159 Transformed cell line Female GM17001 Coriell GM17001 CLO:CLO_0015460,
CLO:CLO_0018044,
BioSample:SAMN00808503,
Coriell:GM03715,
Coriell:GM17001,
Wikidata:Q54838202
CVCL_7401 2026-07-25 04:32:50 0
GM03689
 
Resource Report
Resource Website
RRID:CVCL_X298 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM-3689, GM 3689 CLO:CLO_0015482,
BioSample:SAMN00808497,
Coriell:GM03689,
Wikidata:Q54838190
CVCL_X298 2026-07-25 04:32:50 0
GM03651
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_7396 Homo sapiens (Human) Population: Caucasian. PMID:3863481
PMID:6458814
PMID:6621576
PMID:6726265
PMID:7847674
PMID:8643543
PMID:8823375
PMID:12060391
PMID:21490598
PMID:26984941
PMID:30567591
Finite cell line Female GM3651, GM 3651, GM 03651, GM03651C, GM3651C, AG03651, AG 3651D CLO:CLO_0015448,
BioSample:SAMN00808486,
Coriell:AG03651,
Coriell:GM03651,
GEO:GSM1317021,
GEO:GSM3124679,
Wikidata:Q54838178
CVCL_7396 2026-07-25 04:32:49 0
GM03651
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# AG03651, RRID:CVCL_7396 Homo sapiens (Human) Population: Caucasian. PMID:3863481
PMID:6458814
PMID:6621576
PMID:6726265
PMID:7847674
PMID:8643543
PMID:8823375
PMID:12060391
PMID:21490598
PMID:26984941
PMID:30567591
Finite cell line Female GM3651, GM 3651, GM 03651, GM03651C, GM3651C, AG03651, AG 3651D Coriell AG03651 CLO:CLO_0015448,
BioSample:SAMN00808486,
Coriell:AG03651,
Coriell:GM03651,
GEO:GSM1317021,
GEO:GSM3124679,
Wikidata:Q54838178
CVCL_7396 2026-07-25 04:32:49 0
GM03721
 
Resource Report
Resource Website
RRID:CVCL_M941 Homo sapiens (Human) Population: African American., Part of: Human variation panel. Transformed cell line Female GM17157 CLO:CLO_0013962,
CLO:CLO_0015467,
BioSample:SAMN00808507,
Coriell:GM03721,
Coriell:GM17157,
GEO:GSM273424,
GEO:GSM569659,
GEO:GSM596222,
GEO:GSM597022,
GEO:GSM924667,
Wikidata:Q54838206
CVCL_M941 2026-07-25 04:32:50 0
GM03699
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UY62 Homo sapiens (Human) Finite cell line Female Coriell:GM03699,
Wikidata:Q93585329
CVCL_UY62 2026-07-25 04:32:50 0
GM03722
 
Resource Report
Resource Website
RRID:CVCL_X452 Homo sapiens (Human) Maroteaux-Lamy syndrome Population: African American. Finite cell line Female CLO:CLO_0015465,
BioSample:SAMN00808508,
Coriell:GM03722,
Wikidata:Q54838207
CVCL_X452 2026-07-25 04:32:50 0
GM03651
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM03651, RRID:CVCL_7396 Homo sapiens (Human) Population: Caucasian. PMID:3863481
PMID:6458814
PMID:6621576
PMID:6726265
PMID:7847674
PMID:8643543
PMID:8823375
PMID:12060391
PMID:21490598
PMID:26984941
PMID:30567591
Finite cell line Female GM3651, GM 3651, GM 03651, GM03651C, GM3651C, AG03651, AG 3651D Coriell GM03651 CLO:CLO_0015448,
BioSample:SAMN00808486,
Coriell:AG03651,
Coriell:GM03651,
GEO:GSM1317021,
GEO:GSM3124679,
Wikidata:Q54838178
CVCL_7396 2026-07-25 04:32:49 0
GM03625
 
Resource Report
Resource Website
Coriell Cat# GM03625, RRID:CVCL_2Y87 Homo sapiens (Human) Cartilage hair hypoplasia Population: Caucasian; Amish. Finite cell line Female GM03625B Coriell GM03625 CLO:CLO_0017205,
BioSample:SAMN00808475,
Coriell:GM03625,
Wikidata:Q54838165
CVCL_2Y87 2026-07-25 04:32:49 0
GM03621
 
Resource Report
Resource Website
RRID:CVCL_F063 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6220707 Finite cell line Female GM 3621 CLO:CLO_0017192,
BioSample:SAMN00808472,
Coriell:GM03621,
Wikidata:Q54838162
CVCL_F063 2026-07-25 04:32:49 0

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