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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
GM01671
 
Resource Report
Resource Website
Coriell Cat# GM01671, RRID:CVCL_2Y86 Homo sapiens (Human) Cartilage hair hypoplasia Finite cell line Male GM-1671 Coriell GM01671 CLO:CLO_0030953,
Coriell:GM01671,
Wikidata:Q54837001
CVCL_2Y86 2026-07-25 04:32:21 0
GM01658
 
Resource Report
Resource Website
Coriell Cat# GM01658, RRID:CVCL_2Z69 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Population: Caucasian. Finite cell line Male GM-1658 Coriell GM01658 CLO:CLO_0030940,
BioSample:SAMN00807039,
Coriell:GM01658,
Wikidata:Q54836990
CVCL_2Z69 2026-07-25 04:32:20 0
GM01684
 
Resource Report
Resource Website
RRID:CVCL_U517 Homo sapiens (Human) Citrullinemia type I Population: Caucasian. PMID:7174798 Finite cell line Female GM1684, GM-1684 CLO:CLO_0030968,
BioSample:SAMN00807075,
Coriell:GM01684,
Wikidata:Q54837015
CVCL_U517 2026-07-25 04:32:23 0
GM01722
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JC93 Homo sapiens (Human) Androgen insensitivity syndrome Population: Caucasian. Finite cell line Sex ambiguous GM-1722, GM1722 Coriell:GM01722,
Wikidata:Q54837036
CVCL_JC93 2026-07-25 04:32:24 0
GM01665
 
Resource Report
Resource Website
RRID:CVCL_0Q01 Homo sapiens (Human) Karyotypic information: 46,XX,t(12;21)(12qter->12p11::21p11->21pter;21qter->21p11::12p11->12pter) (Coriell=GM01665)., Population: Caucasian. Finite cell line Female GM-1665 CLO:CLO_0030955,
BioSample:SAMN00807053,
Coriell:GM01665,
Wikidata:Q54836998
CVCL_0Q01 2026-07-25 04:32:21 0
GM01673
 
Resource Report
Resource Website
Coriell Cat# GM01673, RRID:CVCL_0D84 Homo sapiens (Human) Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency Population: Caucasian. PMID:7909321 Finite cell line Male GM1673, GM-1673 Coriell GM01673 CLO:CLO_0030951,
BioSample:SAMN00807059,
Coriell:GM01673,
Wikidata:Q54837006
CVCL_0D84 2026-07-25 04:32:23 0
GM01719
 
Resource Report
Resource Website
RRID:CVCL_9R64 Homo sapiens (Human) PMID:9054950 Finite cell line Female GM-1719, GM1719 CLO:CLO_0030985,
BioSample:SAMN00807107,
Coriell:GM01719,
Wikidata:Q54837033
CVCL_9R64 2026-07-25 04:32:22 0
GM01723
 
Resource Report
Resource Website
RRID:CVCL_X253 Homo sapiens (Human) Population: Caucasian. PMID:6661932 Finite cell line Female GM-1723, GM 1723, GM01723A CLO:CLO_0030980,
BioSample:SAMN00807113,
Coriell:GM01723,
Wikidata:Q54837037
CVCL_X253 2026-07-25 04:32:22 0
GM01706
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_7334 Homo sapiens (Human) Population: Caucasian. PMID:30567591 Finite cell line Female GM1706, GM-1706, GM 1706, GM01706A, GM1706A, GM00237, GM0237 CLO:CLO_0030976,
BioSample:SAMN00807091,
Coriell:GM00237,
Coriell:GM01706,
GEO:GSM3124688,
Wikidata:Q54837025
CVCL_7334 2026-07-25 04:32:24 0
GM01695
 
Resource Report
Resource Website
Coriell Cat# GM01695, RRID:CVCL_V811 Homo sapiens (Human) Duchenne muscular dystrophy Karyotypic information: 46,X,t(X;11)(p21;q13) (PubMed=10377420)., Population: Caucasian. PMID:2498246
PMID:7438786
PMID:10377420
Finite cell line Female GM-1695, GM1695, GM01695A, GM1695A Coriell GM01695 CLO:CLO_0030959,
BioSample:SAMN00807081,
Coriell:GM01695,
Wikidata:Q54837018
CVCL_V811 2026-07-25 04:32:22 0
GM01737
 
Resource Report
Resource Website
Coriell Cat# GM01737, RRID:CVCL_2Z43 Homo sapiens (Human) Campomelic dysplasia Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01737)., Population: Caucasian. Finite cell line Sex ambiguous GM-1737 Coriell GM01737 CLO:CLO_0030995,
BioSample:SAMN00807125,
Coriell:GM01737,
Wikidata:Q54837045
CVCL_2Z43 2026-07-25 04:32:22 0
GM01722
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01722, RRID:CVCL_JC93 Homo sapiens (Human) Androgen insensitivity syndrome Population: Caucasian. Finite cell line Sex ambiguous GM-1722, GM1722 Coriell GM01722 Coriell:GM01722,
Wikidata:Q54837036
CVCL_JC93 2026-07-25 04:32:22 0
GM01672
 
Resource Report
Resource Website
RRID:CVCL_1R60 Homo sapiens (Human) Triploidy syndrome Karyotypic information: 69,XXY (Coriell=GM01672)., Population: Caucasian. PMID:6156493 Finite cell line Male GM-1672, GM 1672 CLO:CLO_0030952,
BioSample:SAMN00807057,
Coriell:GM01672,
Wikidata:Q54837002
CVCL_1R60 2026-07-25 04:32:23 0
GM01664
 
Resource Report
Resource Website
Coriell Cat# GM01664, RRID:CVCL_0Q00 Homo sapiens (Human) Karyotypic information: 46,XY,t(9;13)(9pter->9q13::13q12->13qter;13pter->13q12::9q13->9qter) (Coriell=GM01664)., Population: Caucasian. Finite cell line Male GM-1664 Coriell GM01664 CLO:CLO_0030956,
BioSample:SAMN00807051,
Coriell:GM01664,
Wikidata:Q54836997
CVCL_0Q00 2026-07-25 04:32:23 0
GM01701
 
Resource Report
Resource Website
RRID:CVCL_1D25 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM-1701 CLO:CLO_0030972,
BioSample:SAMN00807085,
Coriell:GM01701,
Wikidata:Q54837021
CVCL_1D25 2026-07-25 04:32:23 0
GM01737
 
Resource Report
Resource Website
RRID:CVCL_2Z43 Homo sapiens (Human) Campomelic dysplasia Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01737)., Population: Caucasian. Finite cell line Sex ambiguous GM-1737 CLO:CLO_0030995,
BioSample:SAMN00807125,
Coriell:GM01737,
Wikidata:Q54837045
CVCL_2Z43 2026-07-25 04:32:25 0
GM01674
 
Resource Report
Resource Website
RRID:CVCL_AW76 Homo sapiens (Human) Methylmalonic aciduria, cblA type Population: Caucasian. Finite cell line Female GM1674, GM-1674, Line 245 CLO:CLO_0030950,
BioSample:SAMN00807061,
Coriell:GM01674,
Wikidata:Q54837007
CVCL_AW76 2026-07-25 04:32:21 0
GM01678
 
Resource Report
Resource Website
RRID:CVCL_0Q02 Homo sapiens (Human) Karyotypic information: 46,XX,t(5;10)(5qter->5p15::10p13->10pter;10qter->10p13::5p15->5pter) (Coriell=GM01678). Finite cell line Female GM-1678 CLO:CLO_0030961,
Coriell:GM01678,
Wikidata:Q54837010
CVCL_0Q02 2026-07-25 04:32:21 0
GM01684
 
Resource Report
Resource Website
Coriell Cat# GM01684, RRID:CVCL_U517 Homo sapiens (Human) Citrullinemia type I Population: Caucasian. PMID:7174798 Finite cell line Female GM1684, GM-1684 Coriell GM01684 CLO:CLO_0030968,
BioSample:SAMN00807075,
Coriell:GM01684,
Wikidata:Q54837015
CVCL_U517 2026-07-25 04:32:21 0
GM01674
 
Resource Report
Resource Website
Coriell Cat# GM01674, RRID:CVCL_AW76 Homo sapiens (Human) Methylmalonic aciduria, cblA type Population: Caucasian. Finite cell line Female GM1674, GM-1674, Line 245 Coriell GM01674 CLO:CLO_0030950,
BioSample:SAMN00807061,
Coriell:GM01674,
Wikidata:Q54837007
CVCL_AW76 2026-07-25 04:32:21 0

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