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95,747 Results - per page

Show More Columns | Download Top 1000 Results

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
GM24068
 
Resource Report
Resource Website
Coriell Cat# GM24068, RRID:CVCL_1B83 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:37751688 Transformed cell line Female Coriell GM24068 Coriell:GM24068,
Wikidata:Q54853510
CVCL_1B83 2026-09-03 06:37:24 0
GM24107
 
Resource Report
Resource Website
RRID:CVCL_1C17 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:37751688 Transformed cell line Female Coriell:GM24107,
Wikidata:Q54853549
CVCL_1C17 2026-09-03 06:37:24 0
GM24027
 
Resource Report
Resource Website
Coriell Cat# GM24027, RRID:CVCL_AE10 Homo sapiens (Human) Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:26621101
PMID:31401124
Transformed cell line Female Coriell GM24027 Coriell:GM24027,
Wikidata:Q54853495
CVCL_AE10 2026-09-03 06:37:23 0
GM24046
 
Resource Report
Resource Website
RRID:CVCL_AY95 Homo sapiens (Human) Transformed cell line Female Coriell:GM24046,
Wikidata:Q54853499
CVCL_AY95 2026-09-03 06:37:23 0
GM24104
 
Resource Report
Resource Website
RRID:CVCL_1C14 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:37751688 Transformed cell line Female Coriell:GM24104,
Wikidata:Q54853546
CVCL_1C14 2026-09-03 06:37:24 0
GM24065
 
Resource Report
Resource Website
RRID:CVCL_U559 Homo sapiens (Human) Prader-Willi syndrome Transformed cell line Female Coriell:GM24065,
Wikidata:Q54853508
CVCL_U559 2026-09-03 06:37:24 0
GM24027
 
Resource Report
Resource Website
RRID:CVCL_AE10 Homo sapiens (Human) Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:26621101
PMID:31401124
Transformed cell line Female Coriell:GM24027,
Wikidata:Q54853495
CVCL_AE10 2026-09-03 06:37:23 0
GM24047
 
Resource Report
Resource Website
RRID:CVCL_Y780 Homo sapiens (Human) Ornithine carbamoyltransferase deficiency disease Transformed cell line Female Coriell:GM24047,
Wikidata:Q54853500
CVCL_Y780 2026-09-03 06:37:24 0
GM24101
 
Resource Report
Resource Website
Coriell Cat# GM24101, RRID:CVCL_1C11 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:37751688 Transformed cell line Female Coriell GM24101 Coriell:GM24101,
Wikidata:Q54853543
CVCL_1C11 2026-09-03 06:37:24 0
GM24101
 
Resource Report
Resource Website
RRID:CVCL_1C11 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:37751688 Transformed cell line Female Coriell:GM24101,
Wikidata:Q54853543
CVCL_1C11 2026-09-03 06:37:24 0
GM24076
 
Resource Report
Resource Website
Coriell Cat# GM24076, RRID:CVCL_1B90 Homo sapiens (Human) Donor information: Donor has a family history of breast cancer but negative for BRCA1 and BRCA2 mutations., Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:37751688 Transformed cell line Female Coriell GM24076 Coriell:GM24076,
Wikidata:Q54853517
CVCL_1B90 2026-09-03 06:37:24 0
GM24107
 
Resource Report
Resource Website
Coriell Cat# GM24107, RRID:CVCL_1C17 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:37751688 Transformed cell line Female Coriell GM24107 Coriell:GM24107,
Wikidata:Q54853549
CVCL_1C17 2026-09-03 06:37:24 0
GM24048
 
Resource Report
Resource Website
Coriell Cat# GM24048, RRID:CVCL_Y781 Homo sapiens (Human) Ornithine carbamoyltransferase deficiency disease Transformed cell line Female Coriell GM24048 Coriell:GM24048,
Wikidata:Q54853501
CVCL_Y781 2026-09-03 06:37:23 0
GM24046
 
Resource Report
Resource Website
Coriell Cat# GM24046, RRID:CVCL_AY95 Homo sapiens (Human) Transformed cell line Female Coriell GM24046 Coriell:GM24046,
Wikidata:Q54853499
CVCL_AY95 2026-09-03 06:37:23 0
GM24061
 
Resource Report
Resource Website
Coriell Cat# GM24061, RRID:CVCL_AY97 Homo sapiens (Human) Turner syndrome Transformed cell line Female Coriell GM24061 Coriell:GM24061,
Wikidata:Q54853507
CVCL_AY97 2026-09-03 06:37:24 0
GM24048
 
Resource Report
Resource Website
RRID:CVCL_Y781 Homo sapiens (Human) Ornithine carbamoyltransferase deficiency disease Transformed cell line Female Coriell:GM24048,
Wikidata:Q54853501
CVCL_Y781 2026-09-03 06:37:23 0
GM24068
 
Resource Report
Resource Website
RRID:CVCL_1B83 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:37751688 Transformed cell line Female Coriell:GM24068,
Wikidata:Q54853510
CVCL_1B83 2026-09-03 06:37:24 0
GM24029
 
Resource Report
Resource Website
RRID:CVCL_AE12 Homo sapiens (Human) Argininosuccinic aciduria Transformed cell line Female Coriell:GM24029,
Wikidata:Q54853497
CVCL_AE12 2026-09-03 06:37:23 0
GM24059
 
Resource Report
Resource Website
Coriell Cat# GM24059, RRID:CVCL_AY96 Homo sapiens (Human) Merosin-deficient congenital muscular dystrophy type 1A Transformed cell line Female Coriell GM24059 Coriell:GM24059,
Wikidata:Q54853506
CVCL_AY96 2026-09-03 06:37:24 0
GM24080
 
Resource Report
Resource Website
RRID:CVCL_1B94 Homo sapiens (Human) Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. PMID:37751688 Transformed cell line Female Coriell:GM24080,
Wikidata:Q54853521
CVCL_1B94 2026-09-03 06:37:24 0

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