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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
GM09307
 
Resource Report
Resource Website
RRID:CVCL_AA04 Homo sapiens (Human) Neurofibromatosis type 2 Transformed cell line Male CLO:CLO_0011913,
Coriell:GM09307,
Wikidata:Q54843667
CVCL_AA04 2026-07-25 04:34:05 0
GM09276
 
Resource Report
Resource Website
RRID:CVCL_IW08 Homo sapiens (Human) Carboxypeptidase N deficiency PMID:12560874 Transformed cell line Male CLO:CLO_0012061,
Coriell:GM09276,
Wikidata:Q54843640
CVCL_IW08 2026-07-25 04:34:03 0
GM09299
 
Resource Report
Resource Website
RRID:CVCL_AA77 Homo sapiens (Human) Familial dysautonomia Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0011874,
Coriell:GM09299,
Wikidata:Q54843659
CVCL_AA77 2026-07-25 04:34:05 0
GM09310
 
Resource Report
Resource Website
RRID:CVCL_8A10 Homo sapiens (Human) Tourette syndrome Transformed cell line Female CLO:CLO_0011914,
Coriell:GM09310,
Wikidata:Q54843668
CVCL_8A10 2026-07-25 04:34:04 0
GM09283
 
Resource Report
Resource Website
RRID:CVCL_N102 Homo sapiens (Human) Population: Puerto Rican., Part of: Human variation panel. Transformed cell line Female GM17076 CLO:CLO_0012059,
CLO:CLO_0014607,
Coriell:GM09283,
Coriell:GM17076,
Wikidata:Q54843643
CVCL_N102 2026-07-25 04:34:03 0
GM09295
 
Resource Report
Resource Website
RRID:CVCL_AA73 Homo sapiens (Human) Familial dysautonomia Population: Jewish; Ashkenazi. Transformed cell line Male CLO:CLO_0011882,
Coriell:GM09295,
Wikidata:Q54843655
CVCL_AA73 2026-07-25 04:34:05 0
GM09310
 
Resource Report
Resource Website
Coriell Cat# GM09310, RRID:CVCL_8A10 Homo sapiens (Human) Tourette syndrome Transformed cell line Female Coriell GM09310 CLO:CLO_0011914,
Coriell:GM09310,
Wikidata:Q54843668
CVCL_8A10 2026-07-25 04:34:05 0
GM09283
 
Resource Report
Resource Website
Coriell Cat# GM17076, RRID:CVCL_N102 Homo sapiens (Human) Population: Puerto Rican., Part of: Human variation panel. Transformed cell line Female GM17076 Coriell GM17076 CLO:CLO_0012059,
CLO:CLO_0014607,
Coriell:GM09283,
Coriell:GM17076,
Wikidata:Q54843643
CVCL_N102 2026-07-25 04:34:03 0
GM09307
 
Resource Report
Resource Website
Coriell Cat# GM09307, RRID:CVCL_AA04 Homo sapiens (Human) Neurofibromatosis type 2 Transformed cell line Male Coriell GM09307 CLO:CLO_0011913,
Coriell:GM09307,
Wikidata:Q54843667
CVCL_AA04 2026-07-25 04:34:04 0
GM09298
 
Resource Report
Resource Website
Coriell Cat# GM09298, RRID:CVCL_AA76 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Male Coriell GM09298 CLO:CLO_0011885,
Coriell:GM09298,
Wikidata:Q54843658
CVCL_AA76 2026-07-25 04:34:04 0
GM09306
 
Resource Report
Resource Website
Coriell Cat# GM17232, RRID:CVCL_N105 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 GM17232 Coriell GM17232 CLO:CLO_0011918,
CLO:CLO_0014344,
Coriell:GM09306,
Coriell:GM17232,
GEO:GSM569607,
GEO:GSM596296,
GEO:GSM596656,
GEO:GSM924834,
Wikidata:Q54843666
CVCL_N105 2026-07-25 04:34:04 0
GM09302
 
Resource Report
Resource Website
Coriell Cat# GM09302, RRID:CVCL_AA79 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Female Coriell GM09302 CLO:CLO_0011875,
Coriell:GM09302,
Wikidata:Q54843662
CVCL_AA79 2026-07-25 04:34:04 0
GM09337
 
Resource Report
Resource Website
Coriell Cat# GM09337, RRID:CVCL_5L72 Homo sapiens (Human) Transformed cell line Female Coriell GM09337 CLO:CLO_0011944,
Coriell:GM09337,
Wikidata:Q54843686
CVCL_5L72 2026-07-25 04:34:04 0
GM09285
 
Resource Report
Resource Website
RRID:CVCL_2T62 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Finite cell line Female CLO:CLO_0012057,
Coriell:GM09285,
Wikidata:Q54843646
CVCL_2T62 2026-07-25 04:34:03 0
GM09316
 
Resource Report
Resource Website
RRID:CVCL_AY32 Homo sapiens (Human) Fragile X syndrome PMID:1672039 Transformed cell line Male GM9316, GM09316A CLO:CLO_0011906,
Coriell:GM09316,
Wikidata:Q54843675
CVCL_AY32 2026-07-25 04:34:05 0
GM09333
 
Resource Report
Resource Website
RRID:CVCL_JE50 Homo sapiens (Human) Wilms tumor Population: Caucasian. Finite cell line Male CLO:CLO_0011942,
Coriell:GM09333,
Wikidata:Q54843684
CVCL_JE50 2026-07-25 04:34:05 0
GM09305
 
Resource Report
Resource Website
RRID:CVCL_AA03 Homo sapiens (Human) Neurofibromatosis type 2 Transformed cell line Male CLO:CLO_0011915,
Coriell:GM09305,
Wikidata:Q54843665
CVCL_AA03 2026-07-25 04:34:04 0
GM09351
 
Resource Report
Resource Website
RRID:CVCL_5L82 Homo sapiens (Human) Tuberous sclerosis 2 Transformed cell line Female CLO:CLO_0011976,
Coriell:GM09351,
Wikidata:Q54843697
CVCL_5L82 2026-07-25 04:34:04 0
GM09287
 
Resource Report
Resource Website
Coriell Cat# GM09287, RRID:CVCL_9S93 Homo sapiens (Human) Trisomy 9 Karyotypic information: 47,XY,+9 (Coriell=GM09287)., Population: African American. Finite cell line Male Coriell GM09287 CLO:CLO_0012045,
Coriell:GM09287,
Wikidata:Q54843648
CVCL_9S93 2026-07-25 04:34:03 0
GM09330
 
Resource Report
Resource Website
RRID:CVCL_8A13 Homo sapiens (Human) Tourette syndrome Transformed cell line Female CLO:CLO_0011946,
Coriell:GM09330,
Wikidata:Q54843681
CVCL_8A13 2026-07-25 04:34:05 0

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