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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
GM09256
 
Resource Report
Resource Website
Coriell Cat# GM09256, RRID:CVCL_V135 Homo sapiens (Human) Population: Caucasian; English/German. PMID:24555846
PMID:25326100
Finite cell line Female GM09256B Coriell GM09256 CLO:CLO_0012022,
Coriell:GM09256,
GEO:GSM1257726,
GEO:GSM1266904,
GEO:GSM1267000,
Wikidata:Q54843638
CVCL_V135 2026-08-15 04:30:44 0
GM09341
 
Resource Report
Resource Website
RRID:CVCL_5L76 Homo sapiens (Human) Tuberous sclerosis 2 Transformed cell line Male CLO:CLO_0011940,
Coriell:GM09341,
Wikidata:Q54843690
CVCL_5L76 2026-08-15 04:30:45 0
GM09257
 
Resource Report
Resource Website
RRID:CVCL_V136 Homo sapiens (Human) Von Hippel-Lindau syndrome Population: Caucasian. PMID:25326100 Finite cell line Female GM09257A CLO:CLO_0012023,
Coriell:GM09257,
GEO:GSM1266905,
Wikidata:Q54843639
CVCL_V136 2026-08-15 04:30:44 0
GM09286
 
Resource Report
Resource Website
Coriell Cat# GM09286, RRID:CVCL_9S92 Homo sapiens (Human) Trisomy 9 Karyotypic information: 47,XY,+9 (Coriell=GM09286)., Population: African American. Finite cell line Male Coriell GM09286 CLO:CLO_0012056,
Coriell:GM09286,
Wikidata:Q54843647
CVCL_9S92 2026-08-15 04:30:44 0
GM09337
 
Resource Report
Resource Website
RRID:CVCL_5L72 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0011944,
Coriell:GM09337,
Wikidata:Q54843686
CVCL_5L72 2026-08-15 04:30:45 0
GM09317
 
Resource Report
Resource Website
Coriell Cat# GM09317, RRID:CVCL_AY33 Homo sapiens (Human) Fragile X syndrome PMID:1672039 Transformed cell line Male GM9317 Coriell GM09317 CLO:CLO_0011905,
Coriell:GM09317,
Wikidata:Q54843676
CVCL_AY33 2026-08-15 04:30:45 0
GM09286
 
Resource Report
Resource Website
RRID:CVCL_9S92 Homo sapiens (Human) Trisomy 9 Karyotypic information: 47,XY,+9 (Coriell=GM09286)., Population: African American. Finite cell line Male CLO:CLO_0012056,
Coriell:GM09286,
Wikidata:Q54843647
CVCL_9S92 2026-08-15 04:30:44 0
GM09293
 
Resource Report
Resource Website
Coriell Cat# GM09293, RRID:CVCL_9X10 Homo sapiens (Human) Population: Caucasian. Transformed cell line Male Coriell GM09293 CLO:CLO_0012042,
Coriell:GM09293,
Wikidata:Q54843652
CVCL_9X10 2026-08-15 04:30:44 0
GM09291
 
Resource Report
Resource Website
RRID:CVCL_9X08 Homo sapiens (Human) Rhizomelic chondrodysplasia punctata Population: Caucasian. Transformed cell line Male CLO:CLO_0012044,
Coriell:GM09291,
Wikidata:Q54843650
CVCL_9X08 2026-08-15 04:30:44 0
GM09348
 
Resource Report
Resource Website
RRID:CVCL_5L80 Homo sapiens (Human) Tuberous sclerosis 2 Transformed cell line Male CLO:CLO_0011966,
Coriell:GM09348,
Wikidata:Q54843695
CVCL_5L80 2026-08-15 04:30:45 0
GM09284
 
Resource Report
Resource Website
RRID:CVCL_N103 Homo sapiens (Human) Population: Puerto Rican., Part of: Human variation panel. Transformed cell line Male GM17077 CLO:CLO_0012058,
CLO:CLO_0014610,
Coriell:GM09284,
Coriell:GM17077,
Wikidata:Q54843645
CVCL_N103 2026-08-15 04:30:44 0
GM09296
 
Resource Report
Resource Website
RRID:CVCL_AA74 Homo sapiens (Human) Familial dysautonomia Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0011883,
Coriell:GM09296,
Wikidata:Q54843656
CVCL_AA74 2026-08-15 04:30:44 0
GM09324
 
Resource Report
Resource Website
Coriell Cat# GM09324, RRID:CVCL_CZ25 Homo sapiens (Human) Karyotypic information: 46,XX,inv(7)(pter->p13::q22->p13::q22->qter) (Coriell=GM09324). Finite cell line Female Coriell GM09324 CLO:CLO_0011911,
Coriell:GM09324,
Wikidata:Q54843677
CVCL_CZ25 2026-08-15 04:30:45 0
GM09283
 
Resource Report
Resource Website
Coriell Cat# GM09283, RRID:CVCL_N102 Homo sapiens (Human) Population: Puerto Rican., Part of: Human variation panel. Transformed cell line Female GM17076 Coriell GM09283 CLO:CLO_0012059,
CLO:CLO_0014607,
Coriell:GM09283,
Coriell:GM17076,
Wikidata:Q54843643
CVCL_N102 2026-08-15 04:30:44 0
GM09300
 
Resource Report
Resource Website
RRID:CVCL_AA78 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0011873,
Coriell:GM09300,
Wikidata:Q54843660
CVCL_AA78 2026-08-15 04:30:44 0
GM09340
 
Resource Report
Resource Website
RRID:CVCL_5L75 Homo sapiens (Human) Tuberous sclerosis 2 Transformed cell line Female CLO:CLO_0011937,
Coriell:GM09340,
Wikidata:Q54843689
CVCL_5L75 2026-08-15 04:30:45 0
GM09285
 
Resource Report
Resource Website
Coriell Cat# GM09285, RRID:CVCL_2T62 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female Coriell GM09285 CLO:CLO_0012057,
Coriell:GM09285,
Wikidata:Q54843646
CVCL_2T62 2026-08-15 04:30:44 0
GM09255
 
Resource Report
Resource Website
Coriell Cat# GM09255, RRID:CVCL_V134 Homo sapiens (Human) Population: Caucasian; English/German. PMID:24555846
PMID:25326100
Finite cell line Male GM09255A Coriell GM09255 CLO:CLO_0012021,
Coriell:GM09255,
GEO:GSM1257725,
GEO:GSM1266903,
GEO:GSM1266999,
Wikidata:Q54843637
CVCL_V134 2026-08-15 04:30:44 0
GM09333
 
Resource Report
Resource Website
Coriell Cat# GM09333, RRID:CVCL_JE50 Homo sapiens (Human) Wilms tumor Population: Caucasian. Finite cell line Male Coriell GM09333 CLO:CLO_0011942,
Coriell:GM09333,
Wikidata:Q54843684
CVCL_JE50 2026-08-15 04:30:45 0
GM09353
 
Resource Report
Resource Website
RRID:CVCL_5L83 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0011975,
Coriell:GM09353,
Wikidata:Q54843698
CVCL_5L83 2026-08-15 04:30:45 0

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