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236,573 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
GM04623
 
Resource Report
Resource Website
RRID:CVCL_AA26 Homo sapiens (Human) Population: Jewish. Finite cell line Female CLO:CLO_0018944,
Coriell:GM04623,
Wikidata:Q54838606
CVCL_AA26 2026-08-08 05:00:17 0
GM04707
 
Resource Report
Resource Website
RRID:CVCL_1I25 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female GM04707A CLO:CLO_0019024,
Coriell:GM04707,
Wikidata:Q54838641
CVCL_1I25 2026-08-08 05:00:18 0
GM04613
 
Resource Report
Resource Website
Coriell Cat# GM04613, RRID:CVCL_1N63 Homo sapiens (Human) Karyotypic information: 46,XY,t(2;11)(2qter->2p11.2::11p13->11pter;11qter->11p13::2p11.2->2pter)mat (Coriell=GM04613)., Population: Caucasian. PMID:2570029 Finite cell line Male GM4613 Coriell GM04613 CLO:CLO_0018903,
Coriell:GM04613,
Wikidata:Q54838599
CVCL_1N63 2026-08-08 05:00:16 0
GM04623
 
Resource Report
Resource Website
Coriell Cat# GM04623, RRID:CVCL_AA26 Homo sapiens (Human) Population: Jewish. Finite cell line Female Coriell GM04623 CLO:CLO_0018944,
Coriell:GM04623,
Wikidata:Q54838606
CVCL_AA26 2026-08-08 05:00:16 0
GM04616
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_V475 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:17668376
Finite cell line Female GM 4616, GM04616A CLO:CLO_0018955,
Coriell:GM04616,
Wikidata:Q54838601
CVCL_V475 2026-08-08 05:00:16 3
GM04619
 
Resource Report
Resource Website
RRID:CVCL_5M96 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Finite cell line Male CLO:CLO_0018945,
Coriell:GM04619,
Wikidata:Q54838604
CVCL_5M96 2026-08-08 05:00:16 0
GM04635
 
Resource Report
Resource Website
RRID:CVCL_M951 Homo sapiens (Human) Population: Jewish; Ashkenazi., Part of: Human variation panel. Transformed cell line Female GM17363 CLO:CLO_0013706,
CLO:CLO_0018972,
Coriell:GM04635,
Coriell:GM17363,
Wikidata:Q54838613
CVCL_M951 2026-08-08 05:00:17 0
GM04674
 
Resource Report
Resource Website
Coriell Cat# GM04674, RRID:CVCL_9R22 Homo sapiens (Human) Population: Caucasian. PMID:19127062 Transformed cell line Female GM04674A Coriell GM04674 CLO:CLO_0019012,
Coriell:GM04674,
Wikidata:Q54838626
CVCL_9R22 2026-08-08 05:00:16 0
GM04710
 
Resource Report
Resource Website
Coriell Cat# GM04710, RRID:CVCL_Y864 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04710A Coriell GM04710 CLO:CLO_0019027,
Coriell:GM04710,
Wikidata:Q54838644
CVCL_Y864 2026-08-08 05:00:17 0
GM04767
 
Resource Report
Resource Website
RRID:CVCL_1I31 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0019050,
Coriell:GM04767,
Wikidata:Q54838671
CVCL_1I31 2026-08-08 05:00:18 0
GM04830
 
Resource Report
Resource Website
RRID:CVCL_1I50 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM04830A, GM04830B CLO:CLO_0018232,
Coriell:GM04830,
Wikidata:Q54838711
CVCL_1I50 2026-08-08 05:00:20 0
GM04796
 
Resource Report
Resource Website
RRID:CVCL_Y884 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female CLO:CLO_0018273,
Coriell:GM04796,
Wikidata:Q54838690
CVCL_Y884 2026-08-08 05:00:18 0
GM04825
 
Resource Report
Resource Website
RRID:CVCL_8A04 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Finite cell line Male CLO:CLO_0018223,
Coriell:GM04825,
Wikidata:Q54838706
CVCL_8A04 2026-08-08 05:00:19 0
GM04791
 
Resource Report
Resource Website
Coriell Cat# GM04791, RRID:CVCL_Y877 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female GM04791A Coriell GM04791 CLO:CLO_0018278,
Coriell:GM04791,
Wikidata:Q54838685
CVCL_Y877 2026-08-08 05:00:18 0
GM04764
 
Resource Report
Resource Website
Coriell Cat# GM04764, RRID:CVCL_8A03 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Transformed cell line Male Coriell GM04764 CLO:CLO_0019048,
Coriell:GM04764,
Wikidata:Q54838669
CVCL_8A03 2026-08-08 05:00:18 0
GM04827
 
Resource Report
Resource Website
Coriell Cat# GM04827, RRID:CVCL_8A05 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Finite cell line Male Coriell GM04827 CLO:CLO_0018235,
Coriell:GM04827,
Wikidata:Q54838707
CVCL_8A05 2026-08-08 05:00:19 0
GM04804
 
Resource Report
Resource Website
RRID:CVCL_Y963 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04804A CLO:CLO_0018212,
Coriell:GM04804,
Wikidata:Q54838696
CVCL_Y963 2026-08-08 05:00:18 0
GM04808
 
Resource Report
Resource Website
Coriell Cat# GM04808, RRID:CVCL_1I44 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM04808A Coriell GM04808 CLO:CLO_0018213,
Coriell:GM04808,
Wikidata:Q54838699
CVCL_1I44 2026-08-08 05:00:18 0
GM04820
 
Resource Report
Resource Website
RRID:CVCL_1I47 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04820A CLO:CLO_0018221,
Coriell:GM04820,
Wikidata:Q54838705
CVCL_1I47 2026-08-08 05:00:19 0
GM04773
 
Resource Report
Resource Website
RRID:CVCL_Y858 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0018255,
Coriell:GM04773,
Wikidata:Q54838673
CVCL_Y858 2026-08-08 05:00:19 0

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