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205 Results - per page

Show More Columns | Download 205 Result(s)

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
BT0001
 
Resource Report
Resource Website
RRID:CVCL_8T85 Homo sapiens (Human) Karyotypic information: 46,XY,del(11)(p14.1) (ECACC=92042901)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Sex ambiguous ECACC:92042901,
Wikidata:Q54798478
CVCL_8T85 2026-07-25 04:22:14 0
BT0001
 
Resource Report
Resource Website
ECACC Cat# 92042901, RRID:CVCL_8T85 Homo sapiens (Human) Karyotypic information: 46,XY,del(11)(p14.1) (ECACC=92042901)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Sex ambiguous ECACC 92042901 ECACC:92042901,
Wikidata:Q54798478
CVCL_8T85 2026-07-25 04:22:14 0
CU0002
 
Resource Report
Resource Website
RRID:CVCL_8U20 Homo sapiens (Human) Campomelic dysplasia Karyotypic information: 46,XY,inv(17)(q11.2;q24.3->q25.1) (ECACC=93092205)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Sex ambiguous ECACC:93092205,
Wikidata:Q54814837
CVCL_8U20 2026-07-25 04:24:44 0
GM00868
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD86 Homo sapiens (Human) 46,XY gonadal dysgenesis Finite cell line Sex ambiguous GM-868 Coriell:GM00868,
Wikidata:Q54836491
CVCL_JD86 2026-07-25 04:32:08 0
GM00868
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00868, RRID:CVCL_JD86 Homo sapiens (Human) 46,XY gonadal dysgenesis Finite cell line Sex ambiguous GM-868 Coriell GM00868 Coriell:GM00868,
Wikidata:Q54836491
CVCL_JD86 2026-07-25 04:32:08 0
GM01404
 
Resource Report
Resource Website
Coriell Cat# GM01404, RRID:CVCL_JC90 Homo sapiens (Human) Androgen insensitivity syndrome Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01404)., Population: African American. Finite cell line Sex ambiguous GM-1404 Coriell GM01404 CLO:CLO_0030807,
BioSample:SAMN00803860,
Coriell:GM01404,
Wikidata:Q54836806
CVCL_JC90 2026-07-25 04:32:18 0
GM01404
 
Resource Report
Resource Website
RRID:CVCL_JC90 Homo sapiens (Human) Androgen insensitivity syndrome Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01404)., Population: African American. Finite cell line Sex ambiguous GM-1404 CLO:CLO_0030807,
BioSample:SAMN00803860,
Coriell:GM01404,
Wikidata:Q54836806
CVCL_JC90 2026-07-25 04:32:16 0
GM01491
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD87 Homo sapiens (Human) 46,XY gonadal dysgenesis Finite cell line Sex ambiguous GM-1491 Coriell:GM01491,
Wikidata:Q54836867
CVCL_JD87 2026-07-25 04:32:17 0
GM01628
 
Resource Report
Resource Website
Coriell Cat# GM01628, RRID:CVCL_DS07 Homo sapiens (Human) 46,XY sex reversal 1 Population: Caucasian. Finite cell line Sex ambiguous GM-1628 Coriell GM01628 CLO:CLO_0031490,
BioSample:SAMN00806989,
Coriell:GM01628,
Wikidata:Q54836962
CVCL_DS07 2026-07-25 04:32:22 0
GM01709
 
Resource Report
Resource Website
RRID:CVCL_X252 Homo sapiens (Human) Gonadal dysgenesis Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Sex ambiguous GM-1709, GM 1709 CLO:CLO_0030969,
BioSample:SAMN00807097,
Coriell:GM01709,
Wikidata:Q54837028
CVCL_X252 2026-07-25 04:32:22 0
GM01721
 
Resource Report
Resource Website
Coriell Cat# GM01721, RRID:CVCL_JC91 Homo sapiens (Human) Androgen insensitivity syndrome Population: Caucasian. Finite cell line Sex ambiguous GM-1721 Coriell GM01721 CLO:CLO_0030979,
BioSample:SAMN00807111,
Coriell:GM01721,
Wikidata:Q54837035
CVCL_JC91 2026-07-25 04:32:22 0
GM01721
 
Resource Report
Resource Website
RRID:CVCL_JC91 Homo sapiens (Human) Androgen insensitivity syndrome Population: Caucasian. Finite cell line Sex ambiguous GM-1721 CLO:CLO_0030979,
BioSample:SAMN00807111,
Coriell:GM01721,
Wikidata:Q54837035
CVCL_JC91 2026-07-25 04:32:22 0
GM01862
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01862, RRID:CVCL_JD89 Homo sapiens (Human) Finite cell line Sex ambiguous GM-1862 Coriell GM01862 Coriell:GM01862,
Wikidata:Q54837135
CVCL_JD89 2026-07-25 04:32:25 0
GM01889
 
Resource Report
Resource Website
Coriell Cat# GM01889, RRID:CVCL_5M70 Homo sapiens (Human) XX male Karyotypic information: 46,XX (Coriell=GM01889)., Population: Caucasian. Finite cell line Sex ambiguous GM-1889 Coriell GM01889 CLO:CLO_0032421,
BioSample:SAMN00807280,
Coriell:GM01889,
Wikidata:Q54837163
CVCL_5M70 2026-07-25 04:32:25 0
GM03368
 
Resource Report
Resource Website
Coriell Cat# GM03368, RRID:CVCL_DS11 Homo sapiens (Human) 46,XY sex reversal 1 Population: African American. Finite cell line Sex ambiguous GM03368-0 Coriell GM03368 CLO:CLO_0016669,
BioSample:SAMN00808373,
Coriell:GM03368,
Wikidata:Q54838029
CVCL_DS11 2026-07-25 04:32:46 0
GM03368-A
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM03368-A, RRID:CVCL_DS12 Homo sapiens (Human) 46,XY sex reversal 1 Population: African American. Finite cell line Sex ambiguous GM03368A Coriell GM03368-A CLO:CLO_0016671,
Coriell:GM03368-A,
Wikidata:Q54838030
CVCL_DS12 2026-07-25 04:32:46 0
GM03547
 
Resource Report
Resource Website
Coriell Cat# GM03547, RRID:CVCL_UR79 Homo sapiens (Human) 17-beta-hydroxysteroid dehydrogenase 3 deficiency Population: Arab. Finite cell line Sex ambiguous Coriell GM03547 CLO:CLO_0017307,
BioSample:SAMN00808445,
Coriell:GM03547,
Wikidata:Q93584700
CVCL_UR79 2026-07-25 04:32:48 0
GM03595
 
Resource Report
Resource Website
RRID:CVCL_X107 Homo sapiens (Human) Karyotypic information: 46,X,del(Y)(pter->q11) [42]; 45,X [8] (Coriell=GM03595)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Sex ambiguous GM 3595 CLO:CLO_0017218,
BioSample:SAMN00808466,
Coriell:GM03595,
Wikidata:Q54838152
CVCL_X107 2026-07-25 04:32:49 0
GM03595
 
Resource Report
Resource Website
Coriell Cat# GM03595, RRID:CVCL_X107 Homo sapiens (Human) Karyotypic information: 46,X,del(Y)(pter->q11) [42]; 45,X [8] (Coriell=GM03595)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Sex ambiguous GM 3595 Coriell GM03595 CLO:CLO_0017218,
BioSample:SAMN00808466,
Coriell:GM03595,
Wikidata:Q54838152
CVCL_X107 2026-07-25 04:32:49 0
GM04435
 
Resource Report
Resource Website
RRID:CVCL_X307 Homo sapiens (Human) Trisomy 16 PMID:6661932
PMID:11687795
Finite cell line Sex ambiguous GM 4435 CLO:CLO_0019688,
Coriell:GM04435,
GEO:GSM803,
Wikidata:Q54838528
CVCL_X307 2026-07-25 04:32:58 0

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