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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
GM00573
 
Resource Report
Resource Website
Coriell Cat# GM00573, RRID:CVCL_1F04 Homo sapiens (Human) Glycogen storage disease type III Population: Caucasian. Finite cell line Female GM-573 Coriell GM00573 CLO:CLO_0026016,
Coriell:GM00573,
Wikidata:Q54836313
CVCL_1F04 2026-08-29 04:27:23 0
GM00562
 
Resource Report
Resource Website
Coriell Cat# GM00562, RRID:CVCL_X233 Homo sapiens (Human) Karyotypic information: 45,X0 [46]; 46,XX [4] (Coriell=GM00562)., Population: African American. PMID:6661932 Finite cell line Female GM-562, GM 562 Coriell GM00562 CLO:CLO_0026020,
Coriell:GM00562,
Wikidata:Q54836309
CVCL_X233 2026-08-29 04:27:23 0
GM00538
 
Resource Report
Resource Website
RRID:CVCL_9W75 Homo sapiens (Human) Maroteaux-Lamy syndrome Population: Caucasian. Finite cell line Female GM-538 CLO:CLO_0026037,
Coriell:GM00538,
Wikidata:Q54836299
CVCL_9W75 2026-08-29 04:27:23 0
GM00509
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L952 Homo sapiens (Human) Karyotypic information: 46,XX,del(13)(pter->q14) (Coriell=GM00509)., Population: African American. PMID:1183234
PMID:6617268
PMID:6661932
PMID:7329430
PMID:7471105
Finite cell line Female GM-509, GM-0509, GM 509, GM00509A, GM 509 A, GM00250, GM-250, GM250 CLO:CLO_0025940,
Coriell:GM00250,
Coriell:GM00509,
Wikidata:Q54836277
CVCL_L952 2026-08-29 04:27:22 0
GM00561
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00561, RRID:CVCL_CX50 Homo sapiens (Human) Finite cell line Female GM-561 Coriell GM00561 Coriell:GM00561,
Wikidata:Q54836308
CVCL_CX50 2026-08-29 04:27:23 0
GM00512
 
Resource Report
Resource Website
Coriell Cat# GM00512, RRID:CVCL_1V21 Homo sapiens (Human) Hurler-Scheie syndrome Population: Indian. Finite cell line Female GM-512 Coriell GM00512 CLO:CLO_0025934,
Coriell:GM00512,
Wikidata:Q54836279
CVCL_1V21 2026-08-29 04:27:23 0
GM00576
 
Resource Report
Resource Website
RRID:CVCL_M923 Homo sapiens (Human) Glycogen storage disease type III Population: Chinese., Part of: Human variation panel. Finite cell line Female GM-576, GM17011 CLO:CLO_0018025,
CLO:CLO_0026023,
Coriell:GM00576,
Coriell:GM17011,
Wikidata:Q54836318
CVCL_M923 2026-08-29 04:27:25 0
GM00546
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM17204, RRID:CVCL_M922 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:62390
PMID:14583597
PMID:16260726
PMID:20889555
PMID:26621101
PMID:29959025
Transformed cell line Female GM-546, GM17204 Coriell GM17204 CLO:CLO_0013835,
Coriell:GM00546,
Coriell:GM17204,
GEO:GSM569628,
GEO:GSM596268,
GEO:GSM596630,
GEO:GSM924806,
Wikidata:Q54836303
CVCL_M922 2026-08-29 04:27:23 0
GM00561
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX50 Homo sapiens (Human) Finite cell line Female GM-561 Coriell:GM00561,
Wikidata:Q54836308
CVCL_CX50 2026-08-29 04:27:23 0
GM00509
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM00509, RRID:CVCL_L952 Homo sapiens (Human) Karyotypic information: 46,XX,del(13)(pter->q14) (Coriell=GM00509)., Population: African American. PMID:1183234
PMID:6617268
PMID:6661932
PMID:7329430
PMID:7471105
Finite cell line Female GM-509, GM-0509, GM 509, GM00509A, GM 509 A, GM00250, GM-250, GM250 Coriell GM00509 CLO:CLO_0025940,
Coriell:GM00250,
Coriell:GM00509,
Wikidata:Q54836277
CVCL_L952 2026-08-29 04:27:22 0
GM00563
 
Resource Report
Resource Website
RRID:CVCL_X234 Homo sapiens (Human) Karyotypic information: 45,X0 (Coriell=GM00563)., Population: African American. PMID:6661932 Finite cell line Female GM-563, GM 563 CLO:CLO_0026021,
Coriell:GM00563,
Wikidata:Q54836310
CVCL_X234 2026-08-29 04:27:23 0
GM00568
 
Resource Report
Resource Website
RRID:CVCL_X446 Homo sapiens (Human) Aspartylglycosaminuria Population: Caucasian; Finnish. PMID:1904874 Finite cell line Female GM-568 CLO:CLO_0026022,
Coriell:GM00568,
Wikidata:Q54836311
CVCL_X446 2026-08-29 04:27:23 0
GM00559
 
Resource Report
Resource Website
RRID:CVCL_AX18 Homo sapiens (Human) Population: Jewish; Ashkenazi. Finite cell line Female GM-559 CLO:CLO_0026019,
Coriell:GM00559,
Wikidata:Q54836306
CVCL_AX18 2026-08-29 04:27:23 0
GM00563
 
Resource Report
Resource Website
Coriell Cat# GM00563, RRID:CVCL_X234 Homo sapiens (Human) Karyotypic information: 45,X0 (Coriell=GM00563)., Population: African American. PMID:6661932 Finite cell line Female GM-563, GM 563 Coriell GM00563 CLO:CLO_0026021,
Coriell:GM00563,
Wikidata:Q54836310
CVCL_X234 2026-08-29 04:27:24 0
GM00519
 
Resource Report
Resource Website
Coriell Cat# GM00519, RRID:CVCL_V775 Homo sapiens (Human) Maroteaux-Lamy syndrome Population: Caucasian. PMID:36611
PMID:806052
PMID:826372
PMID:21418647
PMID:25326100
Finite cell line Female GM-519, GM 519 Coriell GM00519 CLO:CLO_0025937,
Coriell:GM00519,
GEO:GSM651166,
GEO:GSM651167,
GEO:GSM1266911,
GEO:GSM1267005,
Wikidata:Q54836285
CVCL_V775 2026-08-29 04:27:24 0
GM00572
 
Resource Report
Resource Website
RRID:CVCL_1K49 Homo sapiens (Human) Glycogen storage disease type IV Population: Caucasian. PMID:6220706 Finite cell line Female GM-572, GM 0572, GM572 CLO:CLO_0026015,
Coriell:GM00572,
Wikidata:Q54836312
CVCL_1K49 2026-08-29 04:27:23 0
GM00613
 
Resource Report
Resource Website
RRID:CVCL_4D18 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-613 CLO:CLO_0028968,
Coriell:GM00613,
Wikidata:Q54836344
CVCL_4D18 2026-08-29 04:27:24 0
GM00645
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB61 Homo sapiens (Human) Niemann-Pick disease, type C1 Finite cell line Female GM-645 Coriell:GM00645,
Wikidata:Q54836372
CVCL_JB61 2026-08-29 04:27:26 0
GM00593
 
Resource Report
Resource Website
RRID:CVCL_9W76 Homo sapiens (Human) Mucopolysaccharidosis type IVA Population: Mexican. PMID:8910459 Finite cell line Female GM-593 CLO:CLO_0026001,
Coriell:GM00593,
Wikidata:Q54836326
CVCL_9W76 2026-08-29 04:27:25 0
GM00599
 
Resource Report
Resource Website
RRID:CVCL_AA10 Homo sapiens (Human) Familial dysautonomia Transformed cell line Female GM-599, GM00599A CLO:CLO_0029001,
Coriell:GM00599,
Wikidata:Q54836331
CVCL_AA10 2026-08-29 04:27:24 0

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