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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 Authority Record Last Update Mentions Count
GM03782
 
Resource Report
Resource Website
RRID:CVCL_5M85 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian; Iberian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:6726265
PMID:21354051
PMID:23665875
Transformed cell line Male GM 3782, GM3782 CLO:CLO_0015601,
BioSample:SAMN00808530,
Coriell:GM03782,
Wikidata:Q54838232
CVCL_5M85 Cellosaurus 2026-09-26 06:49:10 0
GM03828
 
Resource Report
Resource Website
Coriell Cat# GM03828, RRID:CVCL_X058 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(pter->q21) (Coriell=GM03828)., Population: African American. PMID:6617268
PMID:6661932
Finite cell line Female GM 3828 Coriell GM03828 CLO:CLO_0015676,
BioSample:SAMN00808554,
Coriell:GM03828,
Wikidata:Q54838258
CVCL_X058 Cellosaurus 2026-09-26 06:49:10 0
GM03828
 
Resource Report
Resource Website
RRID:CVCL_X058 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(pter->q21) (Coriell=GM03828)., Population: African American. PMID:6617268
PMID:6661932
Finite cell line Female GM 3828 CLO:CLO_0015676,
BioSample:SAMN00808554,
Coriell:GM03828,
Wikidata:Q54838258
CVCL_X058 Cellosaurus 2026-09-26 06:49:10 0
GM03725
 
Resource Report
Resource Website
RRID:CVCL_7654 Homo sapiens (Human) Population: African American., Part of: Human variation panel. PMID:16260726 Transformed cell line Male GM17103 CLO:CLO_0014898,
CLO:CLO_0015510,
BioSample:SAMN00808511,
Coriell:GM03725,
Coriell:GM17103,
GEO:GSM273373,
GEO:GSM569500,
GEO:GSM596171,
GEO:GSM596972,
GEO:GSM924613,
IPD-IMGT/HLA:15335,
Wikidata:Q54838210
CVCL_7654 Cellosaurus 2026-09-26 06:49:09 0
GM03746
 
Resource Report
Resource Website
RRID:CVCL_1H61 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. Transformed cell line Female CLO:CLO_0015522,
BioSample:SAMN00808516,
Coriell:GM03746,
Wikidata:Q54838215
CVCL_1H61 Cellosaurus 2026-09-26 06:49:10 0
GM03808
 
Resource Report
Resource Website
RRID:CVCL_JE12 Homo sapiens (Human) WAGR syndrome Population: Caucasian. PMID:2559742 Finite cell line Male GM3808, 3808 CLO:CLO_0015562,
BioSample:SAMN00808541,
Coriell:GM03808,
Wikidata:Q54838245
CVCL_JE12 Cellosaurus 2026-09-26 06:49:10 0
GM03809
 
Resource Report
Resource Website
RRID:CVCL_JE58 Homo sapiens (Human) WAGR syndrome PMID:2570029 Finite cell line Female GM3809 CLO:CLO_0015559,
BioSample:SAMN00808542,
Coriell:GM03809,
Wikidata:Q54838246
CVCL_JE58 Cellosaurus 2026-09-26 06:49:10 0
GM03725
 
Resource Report
Resource Website
Coriell Cat# GM03725, RRID:CVCL_7654 Homo sapiens (Human) Population: African American., Part of: Human variation panel. PMID:16260726 Transformed cell line Male GM17103 Coriell GM03725 CLO:CLO_0014898,
CLO:CLO_0015510,
BioSample:SAMN00808511,
Coriell:GM03725,
Coriell:GM17103,
GEO:GSM273373,
GEO:GSM569500,
GEO:GSM596171,
GEO:GSM596972,
GEO:GSM924613,
IPD-IMGT/HLA:15335,
Wikidata:Q54838210
CVCL_7654 Cellosaurus 2026-09-26 06:49:09 0
GM03831
 
Resource Report
Resource Website
Coriell Cat# GM03831, RRID:CVCL_AK82 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Female Coriell GM03831 CLO:CLO_0015674,
BioSample:SAMN00808555,
Coriell:GM03831,
Wikidata:Q54838259
CVCL_AK82 Cellosaurus 2026-09-26 06:49:11 0
GM03876
 
Resource Report
Resource Website
RRID:CVCL_1N78 Homo sapiens (Human) Karyotypic information: 46,XY,t(1;20)(1qter->1p13::20q13.3->20qter;20pter->20q13.3::1p13->1pter) (Coriell=GM03876)., Population: Caucasian. PMID:2535035 Finite cell line Male GM3876 CLO:CLO_0016034,
BioSample:SAMN00808586,
Coriell:GM03876,
Wikidata:Q54838293
CVCL_1N78 Cellosaurus 2026-09-26 06:49:11 0
GM03911
 
Resource Report
Resource Website
RRID:CVCL_AK95 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. PMID:6726265 Transformed cell line Female GM 3911, GM03911A CLO:CLO_0016123,
Coriell:GM03911,
Wikidata:Q54838318
CVCL_AK95 Cellosaurus 2026-09-26 06:49:12 0
GM03910
 
Resource Report
Resource Website
Coriell Cat# GM03910, RRID:CVCL_AK94 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Female Coriell GM03910 CLO:CLO_0015996,
Coriell:GM03910,
Wikidata:Q54838317
CVCL_AK94 Cellosaurus 2026-09-26 06:49:12 0
GM03870
 
Resource Report
Resource Website
RRID:CVCL_1H75 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM03870A CLO:CLO_0016028,
BioSample:SAMN00808582,
Coriell:GM03870,
Wikidata:Q54838289
CVCL_1H75 Cellosaurus 2026-09-26 06:49:11 0
GM03863
 
Resource Report
Resource Website
RRID:CVCL_1H68 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Transformed cell line Female CLO:CLO_0015734,
BioSample:SAMN00808575,
Coriell:GM03863,
Wikidata:Q54838282
CVCL_1H68 Cellosaurus 2026-09-26 06:49:11 0
GM03890
 
Resource Report
Resource Website
RRID:CVCL_W304 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian. Transformed cell line Male GM03890A CLO:CLO_0016007,
BioSample:SAMN00808595,
Coriell:GM03890,
Wikidata:Q54838303
CVCL_W304 Cellosaurus 2026-09-26 06:49:12 0
GM03836
 
Resource Report
Resource Website
Coriell Cat# GM03836, RRID:CVCL_AK87 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. PMID:6726265 Transformed cell line Female GM 3836 Coriell GM03836 CLO:CLO_0015642,
BioSample:SAMN00808560,
Coriell:GM03836,
Wikidata:Q54838264
CVCL_AK87 Cellosaurus 2026-09-26 06:49:11 0
GM03889
 
Resource Report
Resource Website
Coriell Cat# GM03889, RRID:CVCL_W303 Homo sapiens (Human) Usher syndrome type 1 Population: Caucasian. PMID:6726265 Finite cell line Male GM 3889 Coriell GM03889 CLO:CLO_0016010,
BioSample:SAMN00808594,
Coriell:GM03889,
Wikidata:Q54838302
CVCL_W303 Cellosaurus 2026-09-26 06:49:12 0
GM03866
 
Resource Report
Resource Website
Coriell Cat# GM03866, RRID:CVCL_1H71 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Finite cell line Female Coriell GM03866 CLO:CLO_0015710,
BioSample:SAMN00808578,
Coriell:GM03866,
Wikidata:Q54838285
CVCL_1H71 Cellosaurus 2026-09-26 06:49:11 0
GM03869
 
Resource Report
Resource Website
Coriell Cat# GM03869, RRID:CVCL_1H74 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Female Coriell GM03869 CLO:CLO_0016026,
BioSample:SAMN00808581,
Coriell:GM03869,
Wikidata:Q54838288
CVCL_1H74 Cellosaurus 2026-09-26 06:49:11 0
GM03850
 
Resource Report
Resource Website
Coriell Cat# GM03850, RRID:CVCL_AM66 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Caucasian. PMID:7094393 Finite cell line Female GM3850 Coriell GM03850 CLO:CLO_0015631,
BioSample:SAMN00808564,
Coriell:GM03850,
Wikidata:Q54838268
CVCL_AM66 Cellosaurus 2026-09-26 06:49:11 0

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