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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
GM11854
 
Resource Report
Resource Website
RRID:CVCL_7511 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:14583597
PMID:20889555
PMID:29959025
Transformed cell line Male GM 11854, GM17237 CLO:CLO_0014330,
CLO:CLO_0019999,
Coriell:GM11854,
Coriell:GM17237,
GEO:GSM569564,
GEO:GSM596301,
GEO:GSM596661,
GEO:GSM924839,
Wikidata:Q54845298
CVCL_7511 2026-08-15 04:31:27 0
GM11917
 
Resource Report
Resource Website
Coriell Cat# GM11917, RRID:CVCL_R623 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:14583597
PMID:19797678
PMID:20856902
PMID:21397061
Transformed cell line Male Coriell GM11917 CLO:CLO_0020156,
Coriell:GM11917,
GEO:GSM25492,
GEO:GSM25493,
GEO:GSM314874,
GEO:GSM314875,
GEO:GSM420691,
GEO:GSM420692,
GEO:GSM648928,
GEO:GSM906131,
GEO:GSM906132,
IGSR:NA11917,
Wikidata:Q54845350
CVCL_R623 2026-08-15 04:31:28 0
GM11895
 
Resource Report
Resource Website
RRID:CVCL_5C26 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. Transformed cell line Male CLO:CLO_0020029,
Coriell:GM11895,
Wikidata:Q54845334
CVCL_5C26 2026-08-15 04:31:28 0
GM11849
 
Resource Report
Resource Website
RRID:CVCL_1K67 Homo sapiens (Human) Glycogen storage disease type II Population: Caucasian. Finite cell line Male CLO:CLO_0020023,
Coriell:GM11849,
Wikidata:Q54845293
CVCL_1K67 2026-08-15 04:31:27 0
GM11877
 
Resource Report
Resource Website
RRID:CVCL_5C17 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Male CEPH-1347-NA11877, 1347-8443 CLO:CLO_0020044,
Coriell:GM11877,
dbMHC:48633,
GEO:GSM25473,
GEO:GSM420672,
IHW:IHW01106,
IPD-IMGT/HLA:25904,
Wikidata:Q54845309
CVCL_5C17 2026-08-15 04:31:27 0
GM11894
 
Resource Report
Resource Website
Coriell Cat# GM11894, RRID:CVCL_R622 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:21397061
PMID:24037378
PMID:27617755
PMID:29116076
PMID:31048460
Transformed cell line Female Coriell GM11894 CLO:CLO_0020030,
ArrayExpress:E-GEUV-1,
ArrayExpress:E-GEUV-2,
ArrayExpress:E-GEUV-3,
ArrayExpress:E-MTAB-3656,
ArrayExpress:E-MTAB-3657,
ArrayExpress:E-MTAB-5835,
Coriell:GM11894,
GEO:GSM30115,
GEO:GSM648887,
GEO:GSM1719762,
IGSR:NA11894,
Wikidata:Q54845333
CVCL_R622 2026-08-15 04:31:28 0
GM11922
 
Resource Report
Resource Website
RRID:CVCL_5C36 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:14583597
PMID:15514893
PMID:20856902
Transformed cell line Male CLO:CLO_0020162,
Coriell:GM11922,
GEO:GSM25500,
GEO:GSM30206,
GEO:GSM316573,
GEO:GSM316574,
GEO:GSM316575,
GEO:GSM420699,
Wikidata:Q54845355
CVCL_5C36 2026-08-15 04:31:29 0
GM11914
 
Resource Report
Resource Website
RRID:CVCL_5C32 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Female CLO:CLO_0020179,
Coriell:GM11914,
GEO:GSM25489,
GEO:GSM316306,
GEO:GSM316307,
GEO:GSM316308,
GEO:GSM420688,
Wikidata:Q54845347
CVCL_5C32 2026-08-15 04:31:28 0
GM11912
 
Resource Report
Resource Website
Coriell Cat# GM11912, RRID:CVCL_5C30 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Male Coriell GM11912 CLO:CLO_0020185,
Coriell:GM11912,
GEO:GSM25487,
GEO:GSM316564,
GEO:GSM316565,
GEO:GSM316566,
GEO:GSM420686,
Wikidata:Q54845345
CVCL_5C30 2026-08-15 04:31:28 0
GM11872
 
Resource Report
Resource Website
RRID:CVCL_5C13 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:17668376
PMID:20856902
Transformed cell line Male CEPH-1347-NA11872, 1347-8437 CLO:CLO_0020006,
Coriell:GM11872,
dbMHC:48628,
GEO:GSM25470,
GEO:GSM420669,
GEO:GSM659823,
GEO:GSM659911,
GEO:GSM660122,
IHW:IHW01102,
IPD-IMGT/HLA:25900,
Wikidata:Q54845304
CVCL_5C13 2026-08-15 04:31:27 0
GM11853
 
Resource Report
Resource Website
RRID:CVCL_T824 Homo sapiens (Human) Tay-Sachs disease Population: Jewish; Ashkenazi. Finite cell line Male CLO:CLO_0020027,
Coriell:GM11853,
Wikidata:Q54845297
CVCL_T824 2026-08-15 04:31:27 0
GM11887
 
Resource Report
Resource Website
Coriell Cat# GM11887, RRID:CVCL_5C24 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. Transformed cell line Male Coriell GM11887 CLO:CLO_0020035,
Coriell:GM11887,
Wikidata:Q54845328
CVCL_5C24 2026-08-15 04:31:27 0
GM11907
 
Resource Report
Resource Website
RRID:CVCL_IN30 Homo sapiens (Human) Myoclonic epilepsy associated with ragged-red fibers Transformed cell line Female CLO:CLO_0020184,
Coriell:GM11907,
Wikidata:Q54845339
CVCL_IN30 2026-08-15 04:31:28 0
GM11911
 
Resource Report
Resource Website
RRID:CVCL_5C29 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Female CLO:CLO_0020188,
Coriell:GM11911,
GEO:GSM25486,
GEO:GSM316303,
GEO:GSM316304,
GEO:GSM316305,
GEO:GSM420685,
Wikidata:Q54845344
CVCL_5C29 2026-08-15 04:31:28 0
GM11889
 
Resource Report
Resource Website
RRID:CVCL_5C25 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:15514893 Transformed cell line Male CLO:CLO_0020034,
Coriell:GM11889,
GEO:GSM30111,
Wikidata:Q54845329
CVCL_5C25 2026-08-15 04:31:28 0
GM11858
 
Resource Report
Resource Website
Coriell Cat# GM11858, RRID:CVCL_BT24 Homo sapiens (Human) Myasthenia gravis Transformed cell line Male Coriell GM11858 CLO:CLO_0020003,
Coriell:GM11858,
Wikidata:Q54845299
CVCL_BT24 2026-08-15 04:31:27 0
GM11878
 
Resource Report
Resource Website
Coriell Cat# GM11878, RRID:CVCL_5C18 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Male CEPH-1347-NA11878, 1347-8434 Coriell GM11878 CLO:CLO_0020043,
Coriell:GM11878,
dbMHC:48634,
GEO:GSM25474,
GEO:GSM420673,
GEO:GSM659914,
GEO:GSM660125,
GEO:GSM660331,
IHW:IHW01099,
IPD-IMGT/HLA:25897,
Wikidata:Q54845317
CVCL_5C18 2026-08-15 04:31:27 0
GM11955
 
Resource Report
Resource Website
RRID:CVCL_5L12 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0020124,
Coriell:GM11955,
Wikidata:Q54845388
CVCL_5L12 2026-08-15 04:31:29 0
GM11925
 
Resource Report
Resource Website
RRID:CVCL_5C39 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:20856902
Transformed cell line Male CLO:CLO_0020149,
Coriell:GM11925,
GEO:GSM25503,
GEO:GSM30209,
GEO:GSM316579,
GEO:GSM316580,
GEO:GSM316581,
GEO:GSM420702,
Wikidata:Q54845358
CVCL_5C39 2026-08-15 04:31:29 0
GM11953
 
Resource Report
Resource Website
Coriell Cat# GM11953, RRID:CVCL_5L10 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female Coriell GM11953 CLO:CLO_0020126,
Coriell:GM11953,
Wikidata:Q54845386
CVCL_5L10 2026-08-15 04:31:29 0

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