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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
GM05876
 
Resource Report
Resource Website
RRID:CVCL_2Y97 Homo sapiens (Human) 22q11.2 deletion syndrome Population: Caucasian. PMID:23665875 Finite cell line Male CLO:CLO_0024236,
Coriell:GM05876,
Wikidata:Q54841975
CVCL_2Y97 2026-08-01 05:04:52 0
GM05754
 
Resource Report
Resource Website
Coriell Cat# GM05754, RRID:CVCL_4D87 Homo sapiens (Human) Supernumerary circular chromosome Karyotypic information: 46,XY,r(6) [29]; 45,XY,-6 [21] (Coriell=GM05754)., Population: Caucasian. Finite cell line Male Coriell GM05754 CLO:CLO_0024665,
Coriell:GM05754,
Wikidata:Q54841930
CVCL_4D87 2026-08-01 05:04:52 0
GM05878
 
Resource Report
Resource Website
Coriell Cat# GM05878, RRID:CVCL_1Q34 Homo sapiens (Human) Transformed cell line Male Coriell GM05878 CLO:CLO_0024226,
Coriell:GM05878,
Wikidata:Q54841977
CVCL_1Q34 2026-08-01 05:04:58 0
GM05889
 
Resource Report
Resource Website
Coriell Cat# GM05889, RRID:CVCL_4F96 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Finite cell line Male Coriell GM05889 CLO:CLO_0024219,
Coriell:GM05889,
Wikidata:Q54841983
CVCL_4F96 2026-08-01 05:04:59 0
GM05748
 
Resource Report
Resource Website
Coriell Cat# GM05748, RRID:CVCL_F133 Homo sapiens (Human) Farber lipogranulomatosis Population: Caucasian. Transformed cell line Female Coriell GM05748 CLO:CLO_0024638,
Coriell:GM05748,
Wikidata:Q54841925
CVCL_F133 2026-08-01 05:04:56 0
GM05855
 
Resource Report
Resource Website
RRID:CVCL_AX85 Homo sapiens (Human) Transformed cell line Female GM05855B CLO:CLO_0024701,
Coriell:GM05855,
Wikidata:Q54841963
CVCL_AX85 2026-08-01 05:04:59 0
GM05750
 
Resource Report
Resource Website
Coriell Cat# GM05750, RRID:CVCL_X326 Homo sapiens (Human) PMID:6661932
PMID:23665875
Transformed cell line Female GM 5750 Coriell GM05750 CLO:CLO_0024642,
Coriell:GM05750,
Wikidata:Q54841926
CVCL_X326 2026-08-01 05:04:58 0
GM05756
 
Resource Report
Resource Website
RRID:CVCL_7436 Homo sapiens (Human) Population: Caucasian. PMID:2705456
PMID:3745952
PMID:17668376
PMID:33038742
Finite cell line Male GM5756, GM 5756, GM5756A CLO:CLO_0024666,
Coriell:GM05756,
Wikidata:Q54841931
CVCL_7436 2026-08-01 05:04:58 0
GM05877
 
Resource Report
Resource Website
Coriell Cat# GM05877, RRID:CVCL_X140 Homo sapiens (Human) Sporadic retinoblastoma PMID:6661932
PMID:23665875
Finite cell line Female GM 5877 Coriell GM05877 CLO:CLO_0024238,
Coriell:GM05877,
Wikidata:Q54841976
CVCL_X140 2026-08-01 05:04:53 0
GM05889
 
Resource Report
Resource Website
RRID:CVCL_4F96 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Finite cell line Male CLO:CLO_0024219,
Coriell:GM05889,
Wikidata:Q54841983
CVCL_4F96 2026-08-01 05:04:53 0
GM05736
 
Resource Report
Resource Website
Coriell Cat# GM05736, RRID:CVCL_1J28 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM05736A Coriell GM05736 CLO:CLO_0024639,
Coriell:GM05736,
Wikidata:Q54841921
CVCL_1J28 2026-08-01 05:04:58 0
GM05726
 
Resource Report
Resource Website
RRID:CVCL_1J27 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM05726A CLO:CLO_0024647,
Coriell:GM05726,
Wikidata:Q54841920
CVCL_1J27 2026-08-01 05:04:56 0
GM05870
 
Resource Report
Resource Website
RRID:CVCL_7443 Homo sapiens (Human) Medium-chain acyl-CoA dehydrogenase deficiency Population: Caucasian. Finite cell line Female CLO:CLO_0003532,
CLO:CLO_0024232,
CLDB:cl1499,
Coriell:GM05870,
Wikidata:Q54841969
CVCL_7443 2026-08-01 05:04:57 0
GM05847
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_AX82 Homo sapiens (Human) PMID:25776194 Finite cell line Female CLO:CLO_0024703,
Coriell:GM05847,
Wikidata:Q54841958
CVCL_AX82 2026-08-01 05:04:59 0
GM05883
 
Resource Report
Resource Website
RRID:CVCL_GQ57 Homo sapiens (Human) Bipolar disorder Transformed cell line Female CLO:CLO_0024222,
Coriell:GM05883,
Wikidata:Q54841981
CVCL_GQ57 2026-08-01 05:04:58 0
GM05753
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5N34 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell:GM05753,
Wikidata:Q54841929
CVCL_5N34 2026-08-01 05:04:52 0
GM05788
 
Resource Report
Resource Website
RRID:CVCL_7439 Homo sapiens (Human) Smith-Lemli-Opitz syndrome Population: Caucasian. Finite cell line Female CLO:CLO_0024661,
Coriell:GM05788,
Wikidata:Q54841937
CVCL_7439 2026-08-01 05:04:58 0
GM05888
 
Resource Report
Resource Website
RRID:CVCL_4F95 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male GM05888A CLO:CLO_0024220,
Coriell:GM05888,
Wikidata:Q54841982
CVCL_4F95 2026-08-01 05:04:59 0
GM05882
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UT31 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell:GM05882,
Wikidata:Q93790053
CVCL_UT31 2026-08-01 05:04:53 0
GM05750
 
Resource Report
Resource Website
RRID:CVCL_X326 Homo sapiens (Human) PMID:6661932
PMID:23665875
Transformed cell line Female GM 5750 CLO:CLO_0024642,
Coriell:GM05750,
Wikidata:Q54841926
CVCL_X326 2026-08-01 05:04:51 0

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