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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
GM10794
 
Resource Report
Resource Website
Coriell Cat# GM10794, RRID:CVCL_0Q65 Homo sapiens (Human) Karyotypic information: 47,XX,t(4;9)(4pter->4q31.3::9q13->9qter;9pter->9q13::4q31.3->4qter)mat, +der(9)(9pter->9q13::4q31.3->4qter)mat (Coriell=GM10794)., Population: Caucasian. Finite cell line Female Coriell GM10794 CLO:CLO_0023672,
BioSample:SAMN00800194,
Coriell:GM10794,
Wikidata:Q54844639
CVCL_0Q65 2026-08-15 04:31:09 0
GM10809
 
Resource Report
Resource Website
Coriell Cat# GM10809, RRID:CVCL_0R08 Homo sapiens (Human) Adenine phosphoribosyltransferase deficiency Population: Japanese. Transformed cell line Female Coriell GM10809 CLO:CLO_0023807,
BioSample:SAMN00800214,
Coriell:GM10809,
Wikidata:Q54844656
CVCL_0R08 2026-08-15 04:31:09 0
GM10834
 
Resource Report
Resource Website
RRID:CVCL_5B86 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:14583597
PMID:20856902
PMID:30844424
Transformed cell line Female GM10834A, CEPH-1416-NA10834, 1416-1188 CLO:CLO_0023796,
BioSample:SAMN00800232,
Coriell:GM10834,
dbMHC:48703,
GEO:GSM25434,
GEO:GSM25435,
GEO:GSM316444,
GEO:GSM316445,
GEO:GSM316446,
GEO:GSM420600,
GEO:GSM420601,
GEO:GSM905832,
GEO:GSM905927,
GEO:GSM906022,
IHW:IHW01175,
IPD-IMGT/HLA:13832,
Wikidata:Q54844667
CVCL_5B86 2026-08-15 04:31:10 0
GM10837
 
Resource Report
Resource Website
RRID:CVCL_R597 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:20856902
PMID:21397061
Transformed cell line Male CLO:CLO_0023781,
BioSample:SAMN00800238,
Coriell:GM10837,
GEO:GSM25440,
GEO:GSM25441,
GEO:GSM420605,
GEO:GSM648970,
GEO:GSM660010,
GEO:GSM660217,
GEO:GSM660421,
GEO:GSM905834,
GEO:GSM905929,
GEO:GSM906024,
IGSR:NA10837,
Wikidata:Q54844670
CVCL_R597 2026-08-15 04:31:10 0
GM10797
 
Resource Report
Resource Website
Coriell Cat# GM10797, RRID:CVCL_N353 Homo sapiens (Human) Alpha thalassemia Population: Southeast Asian; Filipino. Finite cell line Sex ambiguous Coriell GM10797 CLO:CLO_0023808,
BioSample:SAMN00800198,
Coriell:GM10797,
Wikidata:Q54844641
CVCL_N353 2026-08-15 04:31:09 0
GM10806
 
Resource Report
Resource Website
Coriell Cat# GM10806, RRID:CVCL_2T92 Homo sapiens (Human) Karyotypic information: 46,XX,der(3)(3qter->3p26::2q36->2qter)mat (Coriell=GM10806)., Population: Caucasian. Finite cell line Female Coriell GM10806 CLO:CLO_0023800,
BioSample:SAMN00800208,
Coriell:GM10806,
Wikidata:Q54844647
CVCL_2T92 2026-08-15 04:31:09 0
GM10810
 
Resource Report
Resource Website
RRID:CVCL_N157 Homo sapiens (Human) Adenine phosphoribosyltransferase deficiency Population: Japanese., Part of: Human variation panel. Transformed cell line Male GM17055 CLO:CLO_0014665,
CLO:CLO_0023804,
BioSample:SAMN00800216,
Coriell:GM10810,
Coriell:GM17055,
Wikidata:Q54844657
CVCL_N157 2026-08-15 04:31:09 0
GM10856
 
Resource Report
Resource Website
RRID:CVCL_R611 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:17122850
PMID:19043577
PMID:20856902
PMID:21397061
PMID:23676674
PMID:24924344
PMID:26621101
Transformed cell line Male CLO:CLO_0024097,
BioSample:SAMN00800276,
Coriell:GM10856,
GEO:GSM112504,
GEO:GSM112784,
GEO:GSM188781,
GEO:GSM291615,
GEO:GSM420633,
GEO:GSM648856,
IGSR:NA10856,
Wikidata:Q54844689
CVCL_R611 2026-08-15 04:31:11 0
GM10833
 
Resource Report
Resource Website
Coriell Cat# GM10833, RRID:CVCL_5B85 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Female CEPH-1413-NA10833, 1413-1089 Coriell GM10833 CLO:CLO_0023795,
BioSample:SAMN00800230,
Coriell:GM10833,
dbMHC:48685,
GEO:GSM207761,
GEO:GSM420599,
GEO:GSM660011,
GEO:GSM660218,
GEO:GSM660422,
GEO:GSM905831,
GEO:GSM905926,
GEO:GSM906021,
IHW:IHW01166,
IPD-IMGT/HLA:25960,
Wikidata:Q54844666
CVCL_5B85 2026-08-15 04:31:10 0
GM10840
 
Resource Report
Resource Website
Coriell Cat# GM10840, RRID:CVCL_R600 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:20856902
PMID:21397061
Transformed cell line Female Coriell GM10840 CLO:CLO_0023786,
BioSample:SAMN00800244,
Coriell:GM10840,
GEO:GSM25442,
GEO:GSM25443,
GEO:GSM30193,
GEO:GSM316450,
GEO:GSM316451,
GEO:GSM316452,
GEO:GSM420608,
GEO:GSM420609,
GEO:GSM648960,
GEO:GSM905835,
GEO:GSM905930,
GEO:GSM906025,
IGSR:NA10840,
Wikidata:Q54844673
CVCL_R600 2026-08-15 04:31:10 0
GM10816
 
Resource Report
Resource Website
Coriell Cat# GM10816, RRID:CVCL_0R11 Homo sapiens (Human) Adenine phosphoribosyltransferase deficiency Transformed cell line Female Coriell GM10816 CLO:CLO_0023789,
BioSample:SAMN00800222,
Coriell:GM10816,
Wikidata:Q54844660
CVCL_0R11 2026-08-15 04:31:10 0
GM10791
 
Resource Report
Resource Website
RRID:CVCL_1S04 Cricetulus griseus (Chinese hamster) Characteristics: Hybrid for chromosome 7 mapping. Contains a complete copy of chromosome 7., Group: Human/rodent somatic cell hybrid. PMID:2276735
PMID:8314568
Hybrid cell line 1HL11-G CLO:CLO_0023677,
Coriell:GM10791,
Wikidata:Q54844637
cvcl_1n51 CVCL_1S04 2026-08-15 04:31:09 0
GM10848
 
Resource Report
Resource Website
RRID:CVCL_5B89 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-1332-NA10848, 1332-8260 CLO:CLO_0023759,
BioSample:SAMN00800260,
Coriell:GM10848,
dbMHC:48553,
GEO:GSM420624,
GEO:GSM660028,
GEO:GSM660235,
GEO:GSM660439,
IHW:IHW01029,
IPD-IMGT/HLA:25829,
Wikidata:Q54844681
CVCL_5B89 2026-08-15 04:31:10 0
GM10838
 
Resource Report
Resource Website
RRID:CVCL_R598 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:17122850
PMID:19043577
PMID:20856902
PMID:21397061
PMID:21418647
PMID:24924344
PMID:26621101
Transformed cell line Male CLO:CLO_0023778,
BioSample:SAMN00800240,
Coriell:GM10838,
GEO:GSM112497,
GEO:GSM112777,
GEO:GSM188774,
GEO:GSM291606,
GEO:GSM316402,
GEO:GSM316403,
GEO:GSM316404,
GEO:GSM420606,
GEO:GSM649293,
GEO:GSM651077,
GEO:GSM651078,
GEO:GSM957434,
IGSR:NA10838,
Wikidata:Q54844671
CVCL_R598 2026-08-15 04:31:10 0
GM10847
 
Resource Report
Resource Website
RRID:CVCL_N799 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: ENCODE project common cell types; tier 3., Part of: CEPH/Utah pedigree cell line collection. PMID:17122850
PMID:19043577
PMID:20856902
PMID:23676674
PMID:24037378
PMID:24924344
PMID:26621101
PMID:27617755
PMID:29116076
PMID:30485824
PMID:31048460
Transformed cell line Female CLO:CLO_0023758,
EFO:EFO_0005336,
ArrayExpress:E-GEUV-1,
ArrayExpress:E-GEUV-3,
ArrayExpress:E-MTAB-3656,
ArrayExpress:E-MTAB-3657,
ArrayExpress:E-MTAB-5835,
BioSample:SAMN00800258,
Coriell:GM10847,
ENCODE:ENCBS185AAA,
ENCODE:ENCBS186AAA,
GEO:GSM112500,
GEO:GSM112780,
GEO:GSM188778,
GEO:GSM291610,
GEO:GSM420622,
GEO:GSM420623,
GEO:GSM649294,
GEO:GSM649851,
GEO:GSM1719751,
IGSR:NA10847,
Wikidata:Q54844680
CVCL_N799 2026-08-15 04:31:10 0
GM10812
 
Resource Report
Resource Website
RRID:CVCL_0R10 Homo sapiens (Human) Adenine phosphoribosyltransferase deficiency Population: Japanese. Transformed cell line Female CLO:CLO_0023788,
BioSample:SAMN00800220,
Coriell:GM10812,
Wikidata:Q54844659
CVCL_0R10 2026-08-15 04:31:10 0
GM10793
 
Resource Report
Resource Website
Coriell Cat# GM10793, RRID:CVCL_0Q64 Homo sapiens (Human) Karyotypic information: 47,XX,t(4;9)(4pter->4q31.3::9q13->9qter;9pter->9q13::4q31.3->4qter)mat, +der(9)(9pter->9q13::4q31.3->4qter)mat (Coriell=GM10793)., Population: Caucasian. Finite cell line Female Coriell GM10793 CLO:CLO_0023669,
BioSample:SAMN00800192,
Coriell:GM10793,
Wikidata:Q54844638
CVCL_0Q64 2026-08-15 04:31:09 0
GM10763
 
Resource Report
Resource Website
Coriell Cat# GM10763, RRID:CVCL_4E04 Homo sapiens (Human) Supernumerary circular chromosome Transformed cell line Male Coriell GM10763 CLO:CLO_0023679,
Coriell:GM10763,
Wikidata:Q54844635
CVCL_4E04 2026-08-15 04:31:09 0
GM10798
 
Resource Report
Resource Website
Coriell Cat# GM17084, RRID:CVCL_N155 Homo sapiens (Human) Population: Southeast Asian; Filipino., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Female GM17084 Coriell GM17084 CLO:CLO_0014479,
CLO:CLO_0023798,
BioSample:SAMN00800200,
Coriell:GM10798,
Coriell:GM17084,
Wikidata:Q54844643
CVCL_N155 2026-08-15 04:31:09 0
GM10748
 
Resource Report
Resource Website
RRID:CVCL_V054 Homo sapiens (Human) Marfan syndrome Transformed cell line Female CLO:CLO_0023675,
BioSample:SAMN00800188,
Coriell:GM10748,
Wikidata:Q54844632
CVCL_V054 2026-08-15 04:31:09 0

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