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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
GM01250
 
Resource Report
Resource Website
RRID:CVCL_W636 Homo sapiens (Human) 47,XYY syndrome Karyotypic information: 47,XYY (Coriell=GM01250)., Population: African American. PMID:6661932 Finite cell line Male GM-1250, GM 1250 CLO:CLO_0030931,
BioSample:SAMN00803758,
Coriell:GM01250,
Wikidata:Q54836736
CVCL_W636 2026-08-15 04:28:58 0
GM01225
 
Resource Report
Resource Website
Coriell Cat# GM17022, RRID:CVCL_M984 Homo sapiens (Human) Population: Indian., Part of: Human variation panel. PMID:23665875 Finite cell line Female GM-1225, GM17022 Coriell GM17022 CLO:CLO_0014692,
CLO:CLO_0030280,
BioSample:SAMN00803734,
Coriell:GM01225,
Coriell:GM17022,
Wikidata:Q54836718
CVCL_M984 2026-08-15 04:28:58 0
GM01300
 
Resource Report
Resource Website
RRID:CVCL_2N29 Homo sapiens (Human) Propionic acidemia Finite cell line Female GM1300, GM-1300 CLO:CLO_0030926,
Coriell:GM01300,
Wikidata:Q54836754
CVCL_2N29 2026-08-15 04:28:59 0
GM01261
 
Resource Report
Resource Website
RRID:CVCL_J109 Homo sapiens (Human) Karyotypic information: 45,XX,der(13;18)(13qter->13q10::18q10->18qter) (Coriell=GM01261)., Population: Caucasian. PMID:6661932 Transformed cell line Female GM-1261, GM 1261 CLO:CLO_0030920,
BioSample:SAMN00803780,
Coriell:GM01261,
Wikidata:Q54836748
CVCL_J109 2026-08-15 04:28:59 0
GM01220
 
Resource Report
Resource Website
Coriell Cat# GM01220, RRID:CVCL_V800 Homo sapiens (Human) PMID:891262
PMID:6661932
PMID:23665875
Finite cell line Female GM-1220, GM 1220 Coriell GM01220 CLO:CLO_0030284,
Coriell:GM01220,
Wikidata:Q54836713
CVCL_V800 2026-08-15 04:28:58 0
GM01252
 
Resource Report
Resource Website
RRID:CVCL_V802 Homo sapiens (Human) Population: African American. PMID:477407
PMID:6617268
Finite cell line Female GM-1252, GM 1252 CLO:CLO_0030929,
BioSample:SAMN00803762,
Coriell:GM01252,
Wikidata:Q54836738
CVCL_V802 2026-08-15 04:28:58 0
GM01310
 
Resource Report
Resource Website
RRID:CVCL_7316 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:62390
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Male GM-1310, GM01310B, GM01310C, GM17212 CLO:CLO_0013895,
CLO:CLO_0030914,
BioSample:SAMN00803794,
Coriell:GM01310,
Coriell:GM17212,
GEO:GSM569521,
GEO:GSM596276,
GEO:GSM596637,
GEO:GSM924814,
Wikidata:Q54836762
CVCL_7316 2026-08-15 04:28:59 0
GM01307
 
Resource Report
Resource Website
RRID:CVCL_4F89 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-1307 CLO:CLO_0030916,
BioSample:SAMN00803790,
Coriell:GM01307,
Wikidata:Q54836760
CVCL_4F89 2026-08-15 04:28:59 0
GM01348
 
Resource Report
Resource Website
RRID:CVCL_V211 Homo sapiens (Human) Cystic fibrosis Population: Caucasian. Finite cell line Female GM-1348, GM01348A CLO:CLO_0030900,
BioSample:SAMN00803804,
Coriell:GM01348,
Wikidata:Q54836772
CVCL_V211 2026-08-15 04:28:59 0
GM01255
 
Resource Report
Resource Website
RRID:CVCL_1V24 Homo sapiens (Human) Hurler-Scheie syndrome Population: Caucasian. PMID:6293786 Finite cell line Male GM-1255, GM1255 CLO:CLO_0030934,
BioSample:SAMN00803768,
Coriell:GM01255,
Wikidata:Q54836741
CVCL_1V24 2026-08-15 04:28:58 0
GM01296
 
Resource Report
Resource Website
Coriell Cat# GM01296, RRID:CVCL_0P91 Homo sapiens (Human) Karyotypic information: 45,XX,der(13;15)(13qter->13q10::15q10->15qter) (Coriell=GM01296)., Population: Caucasian. PMID:6293786 Finite cell line Female GM-1296, GM1296, GM01296B Coriell GM01296 CLO:CLO_0030922,
BioSample:SAMN00803784,
Coriell:GM01296,
Wikidata:Q54836750
CVCL_0P91 2026-08-15 04:28:59 0
GM01246
 
Resource Report
Resource Website
RRID:CVCL_H966 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:7313555
PMID:8945471
Transformed cell line Male GM-1246, GM 1246, GM01246A CLO:CLO_0030270,
BioSample:SAMN00803754,
Coriell:GM01246,
Wikidata:Q54836734
CVCL_H966 2026-08-15 04:28:58 0
GM01299
 
Resource Report
Resource Website
RRID:CVCL_2N28 Homo sapiens (Human) Propionic acidemia Finite cell line Male GM1299, GM-1299 CLO:CLO_0030927,
Coriell:GM01299,
Wikidata:Q54836753
CVCL_2N28 2026-08-15 04:28:59 0
GM01228
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM00642, RRID:CVCL_L957 Homo sapiens (Human) Intellectual developmental disorder, X-linked 1 Population: Caucasian. Finite cell line Male GM-1228, GM00642 Coriell GM00642 CLO:CLO_0030282,
BioSample:SAMN00803738,
Coriell:GM00642,
Coriell:GM01228,
Wikidata:Q54836720
CVCL_L957 2026-08-15 04:28:58 0
GM01225
 
Resource Report
Resource Website
RRID:CVCL_M984 Homo sapiens (Human) Population: Indian., Part of: Human variation panel. PMID:23665875 Finite cell line Female GM-1225, GM17022 CLO:CLO_0014692,
CLO:CLO_0030280,
BioSample:SAMN00803734,
Coriell:GM01225,
Coriell:GM17022,
Wikidata:Q54836718
CVCL_M984 2026-08-15 04:28:58 0
GM01302
 
Resource Report
Resource Website
Coriell Cat# GM01302, RRID:CVCL_CX10 Homo sapiens (Human) Glycine encephalopathy Finite cell line Female GM1302, GM-1302 Coriell GM01302 CLO:CLO_0030909,
Coriell:GM01302,
Wikidata:Q54836756
CVCL_CX10 2026-08-15 04:28:59 0
GM01244
 
Resource Report
Resource Website
RRID:CVCL_AI25 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Male GM-1244 CLO:CLO_0030272,
Coriell:GM01244,
Wikidata:Q54836731
CVCL_AI25 2026-08-15 04:28:58 0
GM01323
 
Resource Report
Resource Website
RRID:CVCL_1V18 Homo sapiens (Human) Scheie syndrome Population: Caucasian. Finite cell line Male GM-1323 CLO:CLO_0030899,
BioSample:SAMN00803802,
Coriell:GM01323,
Wikidata:Q54836766
CVCL_1V18 2026-08-15 04:28:59 0
GM01353
 
Resource Report
Resource Website
RRID:CVCL_4N07 Homo sapiens (Human) Cutis laxa Population: Caucasian. PMID:23665875 Finite cell line Male GM-1353 CLO:CLO_0030901,
BioSample:SAMN00803806,
Coriell:GM01353,
Wikidata:Q54836775
CVCL_4N07 2026-08-15 04:28:59 0
GM01257
 
Resource Report
Resource Website
RRID:CVCL_V532 Homo sapiens (Human) Hurler syndrome Population: Caucasian. Finite cell line Female GM-1257 CLO:CLO_0030938,
BioSample:SAMN00803772,
Coriell:GM01257,
Wikidata:Q54836744
CVCL_V532 2026-08-15 04:28:58 0

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