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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
GM09849
 
Resource Report
Resource Website
Coriell Cat# GM09849, RRID:CVCL_GT55 Homo sapiens (Human) Hereditary hemorrhagic telangiectasia Transformed cell line Female Coriell GM09849 CLO:CLO_0030632,
Coriell:GM09849,
Wikidata:Q54844089
CVCL_GT55 2026-09-05 10:56:14 0
GM09825
 
Resource Report
Resource Website
RRID:CVCL_2N14 Homo sapiens (Human) Karyotypic information: 46,X,der(X)(Xpter->Xq21::Yq12->Yqter) (Coriell=GM09825). Finite cell line Female CLO:CLO_0030661,
Coriell:GM09825,
Wikidata:Q54844079
CVCL_2N14 2026-09-05 10:56:14 0
GM09773
 
Resource Report
Resource Website
Coriell Cat# GM09773, RRID:CVCL_AL98 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female Coriell GM09773 CLO:CLO_0030526,
Coriell:GM09773,
Wikidata:Q54844040
CVCL_AL98 2026-09-05 10:56:13 0
GM09777
 
Resource Report
Resource Website
RRID:CVCL_AM02 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female CLO:CLO_0030522,
Coriell:GM09777,
Wikidata:Q54844044
CVCL_AM02 2026-09-05 10:56:13 0
GM09824
 
Resource Report
Resource Website
Coriell Cat# GM09824, RRID:CVCL_2N13 Homo sapiens (Human) PMID:23665875 Finite cell line Female Coriell GM09824 CLO:CLO_0030660,
Coriell:GM09824,
Wikidata:Q54844078
CVCL_2N13 2026-09-05 10:56:14 0
GM09781
 
Resource Report
Resource Website
Coriell Cat# GM09781, RRID:CVCL_AM06 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female Coriell GM09781 CLO:CLO_0030492,
Coriell:GM09781,
Wikidata:Q54844049
CVCL_AM06 2026-09-05 10:56:13 0
GM09833
 
Resource Report
Resource Website
Coriell Cat# GM09833, RRID:CVCL_2Z77 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Karyotypic information: 46,XX,ins(5;15)(5pter->5q23.2::15q23->15q26.1::5q23.2->5qter;15pter->15q23::15q26.1->15qter) (Coriell=GM09833)., Population: Caucasian; Irish. Transformed cell line Female Coriell GM09833 CLO:CLO_0030633,
Coriell:GM09833,
Wikidata:Q54844086
CVCL_2Z77 2026-09-05 10:56:14 0
GM09815
 
Resource Report
Resource Website
RRID:CVCL_N120 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18045 CLO:CLO_0015623,
CLO:CLO_0030663,
Coriell:GM09815,
Coriell:GM18045,
Wikidata:Q54844073
CVCL_N120 2026-09-05 10:56:14 0
GM09794
 
Resource Report
Resource Website
RRID:CVCL_AA99 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0030465,
Coriell:GM09794,
Wikidata:Q54844063
CVCL_AA99 2026-09-05 10:56:14 0
GM09888
 
Resource Report
Resource Website
RRID:CVCL_5P04 Homo sapiens (Human) Trichorhinophalangeal syndrome type II PMID:23665875 Transformed cell line Female CLO:CLO_0030582,
Coriell:GM09888,
Wikidata:Q54844105
CVCL_5P04 2026-09-05 10:56:15 0
GM09867
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_4E00 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0030589,
Coriell:GM09867,
Wikidata:Q54844095
CVCL_4E00 2026-09-05 10:56:14 0
GM09871
 
Resource Report
Resource Website
Coriell Cat# GM17304, RRID:CVCL_N121 Homo sapiens (Human) Population: South American (Andes)., Part of: Human variation panel. Transformed cell line Female GM17304 Coriell GM17304 CLO:CLO_0013315,
CLO:CLO_0030597,
Coriell:GM09871,
Coriell:GM17304,
Wikidata:Q54844100
CVCL_N121 2026-09-05 10:56:15 0
GM09901
 
Resource Report
Resource Website
Coriell Cat# GM18047, RRID:CVCL_N123 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18047 Coriell GM18047 CLO:CLO_0015620,
CLO:CLO_0030552,
Coriell:GM09901,
Coriell:GM18047,
Wikidata:Q54844110
CVCL_N123 2026-09-05 10:56:15 0
GM09885
 
Resource Report
Resource Website
Coriell Cat# GM09885, RRID:CVCL_DS20 Homo sapiens (Human) Sialic acid storage disease Population: Caucasian. Finite cell line Female Coriell GM09885 CLO:CLO_0030601,
Coriell:GM09885,
Wikidata:Q54844102
CVCL_DS20 2026-09-05 10:56:15 0
GM09901
 
Resource Report
Resource Website
RRID:CVCL_N123 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18047 CLO:CLO_0015620,
CLO:CLO_0030552,
Coriell:GM09901,
Coriell:GM18047,
Wikidata:Q54844110
CVCL_N123 2026-09-05 10:56:15 0
GM09888
 
Resource Report
Resource Website
Coriell Cat# GM09888, RRID:CVCL_5P04 Homo sapiens (Human) Trichorhinophalangeal syndrome type II PMID:23665875 Transformed cell line Female Coriell GM09888 CLO:CLO_0030582,
Coriell:GM09888,
Wikidata:Q54844105
CVCL_5P04 2026-09-05 10:56:15 0
GM09899
 
Resource Report
Resource Website
Coriell Cat# GM09899, RRID:CVCL_N122 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 Female GM17233 Coriell GM09899 CLO:CLO_0014338,
CLO:CLO_0030550,
Coriell:GM09899,
Coriell:GM17233,
GEO:GSM569630,
GEO:GSM596297,
GEO:GSM596657,
GEO:GSM924835,
Wikidata:Q54844109
CVCL_N122 2026-09-05 10:56:15 0
GM09915
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UT45 Homo sapiens (Human) PMID:2916654 Transformed cell line Female GM09915A Coriell:GM09915,
Wikidata:Q93806166
CVCL_UT45 2026-09-05 10:56:15 0
GM09887
 
Resource Report
Resource Website
RRID:CVCL_9X49 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female GM09887A CLO:CLO_0030584,
Coriell:GM09887,
Wikidata:Q54844104
CVCL_9X49 2026-09-05 10:56:15 0
GM09864
 
Resource Report
Resource Website
Coriell Cat# GM09864, RRID:CVCL_GT58 Homo sapiens (Human) Hereditary hemorrhagic telangiectasia Transformed cell line Female Coriell GM09864 CLO:CLO_0030627,
Coriell:GM09864,
Wikidata:Q54844093
CVCL_GT58 2026-09-05 10:56:14 0

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