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1,669 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
GM10175
 
Resource Report
Resource Website
RRID:CVCL_2T73 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0029315,
BioSample:SAMN00799797,
Coriell:GM10175,
Wikidata:Q54844278
CVCL_2T73 2026-02-14 08:16:55 0
GM10313
 
Resource Report
Resource Website
RRID:CVCL_2T80 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0029047,
Coriell:GM10313,
Wikidata:Q54844373
CVCL_2T80 2026-02-14 08:16:58 0
GM10283
 
Resource Report
Resource Website
RRID:CVCL_5P16 Homo sapiens (Human) Hyperglycerolemia Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Transformed cell line Male CLO:CLO_0029163,
BioSample:SAMN00799887,
Coriell:GM10283,
Wikidata:Q54844348
CVCL_5P16 2026-02-14 08:16:57 0
GM10313
 
Resource Report
Resource Website
Coriell Cat# GM10313, RRID:CVCL_2T80 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM10313 CLO:CLO_0029047,
Coriell:GM10313,
Wikidata:Q54844373
CVCL_2T80 2026-02-14 08:16:58 0
GM10266
 
Resource Report
Resource Website
Coriell Cat# GM10266, RRID:CVCL_L246 Homo sapiens (Human) Cornelia de Lange syndrome Part of: ENCODE project common cell types; tier 3. PMID:23665875 Transformed cell line Male Coriell GM10266 CLO:CLO_0029187,
EFO:EFO_0005335,
BioSample:SAMN00799865,
Coriell:GM10266,
ENCODE:ENCBS184AAA,
GEO:GSM1008590,
Wikidata:Q54844334
CVCL_L246 2026-02-14 08:16:57 0
GM10329
 
Resource Report
Resource Website
Coriell Cat# GM10329, RRID:CVCL_2T81 Homo sapiens (Human) Population: African American. PMID:23665875 Finite cell line Male Coriell GM10329 CLO:CLO_0029062,
BioSample:SAMN00799920,
Coriell:GM10329,
Wikidata:Q54844381
CVCL_2T81 2026-02-14 08:16:58 0
GM10284
 
Resource Report
Resource Website
RRID:CVCL_4E02 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Male CLO:CLO_0029155,
BioSample:SAMN00799889,
Coriell:GM10284,
Wikidata:Q54844349
CVCL_4E02 2026-02-14 08:16:57 0
GM10266
 
Resource Report
Resource Website
RRID:CVCL_L246 Homo sapiens (Human) Cornelia de Lange syndrome Part of: ENCODE project common cell types; tier 3. PMID:23665875 Transformed cell line Male CLO:CLO_0029187,
EFO:EFO_0005335,
BioSample:SAMN00799865,
Coriell:GM10266,
ENCODE:ENCBS184AAA,
GEO:GSM1008590,
Wikidata:Q54844334
CVCL_L246 2026-02-14 08:16:57 0
GM10401
 
Resource Report
Resource Website
Coriell Cat# GM10401, RRID:CVCL_5P17 Homo sapiens (Human) Karyotypic information: 47,XX,+2.arr(2p)x3 (Coriell=GM10401)., Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM10401 CLO:CLO_0028679,
BioSample:SAMN00799991,
Coriell:GM10401,
Wikidata:Q54844434
CVCL_5P17 2026-02-14 08:17:00 0
GM10401
 
Resource Report
Resource Website
RRID:CVCL_5P17 Homo sapiens (Human) Karyotypic information: 47,XX,+2.arr(2p)x3 (Coriell=GM10401)., Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0028679,
BioSample:SAMN00799991,
Coriell:GM10401,
Wikidata:Q54844434
CVCL_5P17 2026-02-14 08:17:00 0
GM10374
 
Resource Report
Resource Website
Coriell Cat# GM10374, RRID:CVCL_2T82 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM10374 CLO:CLO_0028597,
BioSample:SAMN00799963,
Coriell:GM10374,
Wikidata:Q54844420
CVCL_2T82 2026-02-14 08:16:59 0
GM10384
 
Resource Report
Resource Website
Coriell Cat# GM10384, RRID:CVCL_N142 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:23665875
PMID:29959025
Transformed cell line Female GM17293 Coriell GM10384 CLO:CLO_0013137,
CLO:CLO_0028566,
BioSample:SAMN00799975,
Coriell:GM10384,
Coriell:GM17293,
GEO:GSM569761,
GEO:GSM596357,
GEO:GSM596815,
GEO:GSM924895,
Wikidata:Q54844426
CVCL_N142 2026-02-14 08:16:59 0
GM10382
 
Resource Report
Resource Website
Coriell Cat# GM10382, RRID:CVCL_0I28 Homo sapiens (Human) 22q11.2 deletion syndrome Population: Caucasian. PMID:23665875 Finite cell line Male GM10382A Coriell GM10382 CLO:CLO_0028575,
BioSample:SAMN00799971,
Coriell:GM10382,
Wikidata:Q54844424
CVCL_0I28 2026-02-14 08:16:59 0
GM10636
 
Resource Report
Resource Website
Coriell Cat# GM10636, RRID:CVCL_5P23 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM10636 CLO:CLO_0024562,
BioSample:SAMN00800120,
Coriell:GM10636,
Wikidata:Q54844566
CVCL_5P23 2026-02-14 08:17:03 0
GM10557
 
Resource Report
Resource Website
Coriell Cat# GM10557, RRID:CVCL_5P18 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM10557 CLO:CLO_0024290,
BioSample:SAMN00800085,
Coriell:GM10557,
Wikidata:Q54844542
CVCL_5P18 2026-02-14 08:17:02 0
GM10608
 
Resource Report
Resource Website
Coriell Cat# GM10608, RRID:CVCL_5P22 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM10608 CLO:CLO_0024284,
Coriell:GM10608,
Wikidata:Q54844551
CVCL_5P22 2026-02-14 08:17:02 0
GM10607
 
Resource Report
Resource Website
RRID:CVCL_2T86 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0024283,
BioSample:SAMN00800099,
Coriell:GM10607,
Wikidata:Q54844550
CVCL_2T86 2026-02-14 08:17:02 0
GM10557
 
Resource Report
Resource Website
RRID:CVCL_5P18 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0024290,
BioSample:SAMN00800085,
Coriell:GM10557,
Wikidata:Q54844542
CVCL_5P18 2026-02-14 08:17:02 0
GM10609
 
Resource Report
Resource Website
Coriell Cat# GM10609, RRID:CVCL_0R05 Homo sapiens (Human) Greig syndrome PMID:23665875 Transformed cell line Female GM10609A Coriell GM10609 CLO:CLO_0024279,
Coriell:GM10609,
Wikidata:Q54844552
CVCL_0R05 2026-02-14 08:17:02 0
GM10607
 
Resource Report
Resource Website
Coriell Cat# GM10607, RRID:CVCL_2T86 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM10607 CLO:CLO_0024283,
BioSample:SAMN00800099,
Coriell:GM10607,
Wikidata:Q54844550
CVCL_2T86 2026-02-14 08:17:02 0

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