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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
GM03886
 
Resource Report
Resource Website
RRID:CVCL_2S98 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;9)(4pter->4q33::9q12->9qter;9pter->9q12::4q33->4qter) (Coriell=GM03886)., Population: Caucasian. Finite cell line Female CLO:CLO_0016012,
BioSample:SAMN00808592,
Coriell:GM03886,
Wikidata:Q54838300
CVCL_2S98 2026-07-25 04:32:53 0
GM03860
 
Resource Report
Resource Website
RRID:CVCL_1H65 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0015729,
BioSample:SAMN00808572,
Coriell:GM03860,
Wikidata:Q54838276
CVCL_1H65 2026-07-25 04:32:52 0
GM03865
 
Resource Report
Resource Website
Coriell Cat# GM03865, RRID:CVCL_1H70 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Female Coriell GM03865 CLO:CLO_0015737,
BioSample:SAMN00808577,
Coriell:GM03865,
Wikidata:Q54838284
CVCL_1H70 2026-07-25 04:32:52 0
GM03868
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM03868, RRID:CVCL_1H73 Homo sapiens (Human) Huntington's disease Population: Caucasian. Finite cell line Female Coriell GM03868 CLO:CLO_0016025,
BioSample:SAMN00808580,
Coriell:GM03868,
Wikidata:Q54838287
CVCL_1H73 2026-07-25 04:32:52 1
GM03837
 
Resource Report
Resource Website
Coriell Cat# GM03837, RRID:CVCL_AK88 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Female Coriell GM03837 CLO:CLO_0015639,
BioSample:SAMN00808561,
Coriell:GM03837,
Wikidata:Q54838265
CVCL_AK88 2026-07-25 04:32:52 0
GM03851
 
Resource Report
Resource Website
Coriell Cat# GM03851, RRID:CVCL_GY19 Homo sapiens (Human) Leber congenital amaurosis Population: Caucasian. Transformed cell line Female Coriell GM03851 CLO:CLO_0015629,
BioSample:SAMN00808565,
Coriell:GM03851,
Wikidata:Q54838269
CVCL_GY19 2026-07-25 04:32:52 0
GM04088
 
Resource Report
Resource Website
RRID:CVCL_2T00 Homo sapiens (Human) Karyotypic information: 46,XX,t(1;4)(1pter->1q32::4p16->4pter;4qter->4p16::1q32->1qter) (Coriell=GM04088)., Population: Caucasian. Finite cell line Female CLO:CLO_0016221,
Coriell:GM04088,
Wikidata:Q54838385
CVCL_2T00 2026-07-25 04:32:55 0
GM03953
 
Resource Report
Resource Website
RRID:CVCL_CY42 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Transformed cell line Female CLO:CLO_0016095,
Coriell:GM03953,
Wikidata:Q54838348
CVCL_CY42 2026-07-25 04:32:54 0
GM04053
 
Resource Report
Resource Website
RRID:CVCL_V240 Ovis aries (Sheep) Finite cell line Female CLO:CLO_0016220,
Coriell:GM04053,
Wikidata:Q54838380
CVCL_V240 2026-07-25 04:32:54 0
GM04081
 
Resource Report
Resource Website
RRID:CVCL_0R01 Homo sapiens (Human) Primary carnitine deficiency Population: Caucasian. Finite cell line Male CLO:CLO_0016224,
Coriell:GM04081,
Wikidata:Q54838384
CVCL_0R01 2026-07-25 04:32:55 0
GM04126
 
Resource Report
Resource Website
RRID:CVCL_V820 Homo sapiens (Human) Wolf-Hirschhorn syndrome Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM 4126 CLO:CLO_0016204,
Coriell:GM04126,
Wikidata:Q54838392
CVCL_V820 2026-07-25 04:32:55 0
GM04079
 
Resource Report
Resource Website
RRID:CVCL_T821 Homo sapiens (Human) Friedreich ataxia Caution: Indicated by Coriell to have 420 and 541 GAA repeats., Population: Caucasian. Transformed cell line Male CLO:CLO_0016225,
Coriell:GM04079,
Wikidata:Q54838383
CVCL_T821 2026-07-25 04:32:55 0
GM03928
 
Resource Report
Resource Website
RRID:CVCL_N013 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18013 CLO:CLO_0016014,
CLO:CLO_0016138,
Coriell:GM03928,
Coriell:GM18013,
Wikidata:Q54838328
CVCL_N013 2026-07-25 04:32:53 0
GM03928
 
Resource Report
Resource Website
Coriell Cat# GM18013, RRID:CVCL_N013 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18013 Coriell GM18013 CLO:CLO_0016014,
CLO:CLO_0016138,
Coriell:GM03928,
Coriell:GM18013,
Wikidata:Q54838328
CVCL_N013 2026-07-25 04:32:53 0
GM03998
 
Resource Report
Resource Website
RRID:CVCL_IZ39 Homo sapiens (Human) Hyperlipoproteinemia, type I Population: Caucasian. Finite cell line Male CLO:CLO_0016074,
Coriell:GM03998,
Wikidata:Q54838364
CVCL_IZ39 2026-07-25 04:32:54 0
GM03940
 
Resource Report
Resource Website
RRID:CVCL_CY31 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Finite cell line Male CLO:CLO_0016105,
Coriell:GM03940,
Wikidata:Q54838334
CVCL_CY31 2026-07-25 04:32:53 0
GM03944
 
Resource Report
Resource Website
RRID:CVCL_CY35 Homo sapiens (Human) Familial adenomatous polyposis Population: Caucasian. Finite cell line Female CLO:CLO_0016109,
Coriell:GM03944,
Wikidata:Q54838339
CVCL_CY35 2026-07-25 04:32:54 0
GM04025
 
Resource Report
Resource Website
RRID:CVCL_1N28 Homo sapiens (Human) Fragile X syndrome Population: African American. PMID:1672039
PMID:25776194
PMID:33426406
Transformed cell line Male GM4025B, GM04025C, GM04025E CLO:CLO_0016229,
Coriell:GM04025,
Wikidata:Q54838374
CVCL_1N28 2026-07-25 04:32:54 0
GM03941
 
Resource Report
Resource Website
Coriell Cat# GM03941, RRID:CVCL_CY32 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Transformed cell line Male GM03941B Coriell GM03941 CLO:CLO_0016108,
Coriell:GM03941,
Wikidata:Q54838336
CVCL_CY32 2026-07-25 04:32:53 0
GM03918
 
Resource Report
Resource Website
RRID:CVCL_X115 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM 3918 CLO:CLO_0016128,
Coriell:GM03918,
Wikidata:Q54838326
CVCL_X115 2026-07-25 04:32:53 0

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