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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
GM05368
 
Resource Report
Resource Website
Coriell Cat# GM05368, RRID:CVCL_0Q55 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell GM05368 CLO:CLO_0024872,
Coriell:GM05368,
Wikidata:Q54838984
CVCL_0Q55 2026-08-01 05:04:46 0
GM05387
 
Resource Report
Resource Website
Coriell Cat# GM05387, RRID:CVCL_7421 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM5387 Coriell GM05387 CLO:CLO_0024850,
Coriell:GM05387,
Wikidata:Q54838998
CVCL_7421 2026-08-01 05:04:50 0
GM05400
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM05400, RRID:CVCL_7426 Homo sapiens (Human) Population: African American. PMID:25059784
PMID:26831110
PMID:30567591
PMID:34746695
Finite cell line Male GM5400, C2 Coriell GM05400 CLO:CLO_0024821,
CLO:CLO_0037443,
Coriell:GM05400,
GEO:GSM3124630,
LINCS_LDP:LPC-1044,
Wikidata:Q54839006
CVCL_7426 2026-08-01 05:04:50 2
GM05442
 
Resource Report
Resource Website
RRID:CVCL_1I81 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM05442B CLO:CLO_0024808,
Coriell:GM05442,
Wikidata:Q54839022
CVCL_1I81 2026-08-01 05:04:47 0
GM05399
 
Resource Report
Resource Website
RRID:CVCL_7425 Homo sapiens (Human) Population: Caucasian. PMID:2705456
PMID:25732146
Finite cell line Male GM5399 CLO:CLO_0024823,
Coriell:GM05399,
Wikidata:Q54839005
CVCL_7425 2026-08-01 05:04:50 0
GM05401
 
Resource Report
Resource Website
RRID:CVCL_X324 Homo sapiens (Human) 22q11.2 deletion syndrome Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM 5401 CLO:CLO_0024825,
Coriell:GM05401,
Wikidata:Q54839007
CVCL_X324 2026-08-01 05:04:47 0
GM05380
 
Resource Report
Resource Website
Coriell Cat# GM05380, RRID:CVCL_7418 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 GM17257 Coriell GM05380 CLO:CLO_0014393,
CLO:CLO_0024839,
Coriell:GM05380,
Coriell:GM17257,
GEO:GSM569645,
GEO:GSM596321,
GEO:GSM596680,
GEO:GSM924859,
Wikidata:Q54838994
CVCL_7418 2026-08-01 05:04:50 0
GM05447
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM05447, RRID:CVCL_UT22 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male GM05447Z Coriell GM05447 Coriell:GM05447,
Wikidata:Q93789001
CVCL_UT22 2026-08-01 05:04:47 0
GM05379
 
Resource Report
Resource Website
RRID:CVCL_AL06 Homo sapiens (Human) Retinitis pigmentosa Transformed cell line Female CLO:CLO_0024840,
Coriell:GM05379,
Wikidata:Q54838993
CVCL_AL06 2026-08-01 05:04:50 0
GM05366
 
Resource Report
Resource Website
Coriell Cat# GM05366, RRID:CVCL_0P56 Homo sapiens (Human) Hepatolenticular degeneration Population: Caucasian. Finite cell line Female GM05366A Coriell GM05366 CLO:CLO_0024870,
Coriell:GM05366,
Wikidata:Q54838982
CVCL_0P56 2026-08-01 05:04:49 0
GM05367
 
Resource Report
Resource Website
RRID:CVCL_0P57 Homo sapiens (Human) Hepatolenticular degeneration Population: Caucasian. Transformed cell line Female CLO:CLO_0024873,
Coriell:GM05367,
Wikidata:Q54838983
CVCL_0P57 2026-08-01 05:04:46 0
GM05377
 
Resource Report
Resource Website
RRID:CVCL_7417 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 GM17256 CLO:CLO_0014396,
CLO:CLO_0024842,
Coriell:GM05377,
Coriell:GM17256,
GEO:GSM569660,
GEO:GSM596320,
GEO:GSM596679,
GEO:GSM924858,
Wikidata:Q54838989
CVCL_7417 2026-08-01 05:04:46 0
GM05392
 
Resource Report
Resource Website
RRID:CVCL_F293 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM05392A, GM17258 CLO:CLO_0014394,
CLO:CLO_0024810,
Coriell:GM05392,
Coriell:GM17258,
GEO:GSM569653,
GEO:GSM596322,
GEO:GSM596681,
GEO:GSM924860,
Wikidata:Q54839001
CVCL_F293 2026-08-01 05:04:52 0
GM05404
 
Resource Report
Resource Website
RRID:CVCL_AW68 Homo sapiens (Human) Dystrophia myotonica 1 Finite cell line Female CLO:CLO_0024824,
Coriell:GM05404,
Wikidata:Q54839008
CVCL_AW68 2026-08-01 05:04:50 0
GM05448
 
Resource Report
Resource Website
RRID:CVCL_1I82 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male CLO:CLO_0024806,
Coriell:GM05448,
Wikidata:Q54839023
CVCL_1I82 2026-08-01 05:04:53 0
GM05448
 
Resource Report
Resource Website
Coriell Cat# GM05448, RRID:CVCL_1I82 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male Coriell GM05448 CLO:CLO_0024806,
Coriell:GM05448,
Wikidata:Q54839023
CVCL_1I82 2026-08-01 05:04:51 0
GM05408
 
Resource Report
Resource Website
Coriell Cat# GM17260, RRID:CVCL_7427 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 GM17260 Coriell GM17260 CLO:CLO_0013182,
CLO:CLO_0024816,
Coriell:GM05408,
Coriell:GM17260,
GEO:GSM569646,
GEO:GSM596324,
GEO:GSM596683,
GEO:GSM924862,
Wikidata:Q54839010
CVCL_7427 2026-08-01 05:04:47 0
GM05388
 
Resource Report
Resource Website
Coriell Cat# GM05388, RRID:CVCL_7422 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM5388 Coriell GM05388 CLO:CLO_0024848,
Coriell:GM05388,
Wikidata:Q54838999
CVCL_7422 2026-08-01 05:04:52 0
GM05398
 
Resource Report
Resource Website
Coriell Cat# GM17259, RRID:CVCL_7424 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:18485778 Transformed cell line Male GM05398A, GM17259 Coriell GM17259 CLO:CLO_0014388,
CLO:CLO_0024811,
Coriell:GM05398,
Coriell:GM17259,
GEO:GSM569654,
GEO:GSM596323,
GEO:GSM596682,
GEO:GSM924861,
Wikidata:Q54839004
CVCL_7424 2026-08-01 05:04:52 0
GM05409
 
Resource Report
Resource Website
RRID:CVCL_2T13 Homo sapiens (Human) Karyotypic information: 46,XY,t(5;17)(5pter->5q33::17p12->17pter;17qter->17p12::5q33->5qter) (Coriell=GM05409)., Population: Caucasian. Finite cell line Male CLO:CLO_0024797,
Coriell:GM05409,
Wikidata:Q54839011
CVCL_2T13 2026-08-01 05:04:53 0

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