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95,747 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
DD3502
 
Resource Report
Resource Website
ECACC Cat# 00021514, RRID:CVCL_9P80 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00021514 ECACC:00021514,
Wikidata:Q54830768
CVCL_9P80 2026-07-25 04:30:15 0
DD3508
 
Resource Report
Resource Website
ECACC Cat# 00021614, RRID:CVCL_9P84 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00021614 ECACC:00021614,
Wikidata:Q54830772
CVCL_9P84 2026-07-25 04:30:15 0
DD3481
 
Resource Report
Resource Website
RRID:CVCL_9N12 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:99120302,
Wikidata:Q54830762
CVCL_9N12 2026-07-25 04:30:15 0
DD3466
 
Resource Report
Resource Website
RRID:CVCL_9P72 Homo sapiens (Human) Karyotypic information: 46,XX,t(10;11)(q24.?31;p15.5); de novo (ECACC=99092423)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:99092423,
Wikidata:Q54830755
CVCL_9P72 2026-07-25 04:30:15 0
DD3542
 
Resource Report
Resource Website
RRID:CVCL_9N24 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:00050408,
Wikidata:Q54830795
CVCL_9N24 2026-07-25 04:30:16 0
DD3551
 
Resource Report
Resource Website
ECACC Cat# 00060705, RRID:CVCL_9P96 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00060705 ECACC:00060705,
Wikidata:Q54830802
CVCL_9P96 2026-07-25 04:30:16 0
DD3520
 
Resource Report
Resource Website
ECACC Cat# 00031405, RRID:CVCL_9P89 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00031405 ECACC:00031405,
Wikidata:Q54830784
CVCL_9P89 2026-07-25 04:30:15 0
DD3466
 
Resource Report
Resource Website
ECACC Cat# 99092423, RRID:CVCL_9P72 Homo sapiens (Human) Karyotypic information: 46,XX,t(10;11)(q24.?31;p15.5); de novo (ECACC=99092423)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 99092423 ECACC:99092423,
Wikidata:Q54830755
CVCL_9P72 2026-07-25 04:30:15 0
DD3542
 
Resource Report
Resource Website
ECACC Cat# 00050408, RRID:CVCL_9N24 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 00050408 ECACC:00050408,
Wikidata:Q54830795
CVCL_9N24 2026-07-25 04:30:16 0
DD3532
 
Resource Report
Resource Website
ECACC Cat# 00041223, RRID:CVCL_9N19 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00041223 ECACC:00041223,
Wikidata:Q54830789
CVCL_9N19 2026-07-25 04:30:16 0
DD3551
 
Resource Report
Resource Website
RRID:CVCL_9P96 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:00060705,
Wikidata:Q54830802
CVCL_9P96 2026-07-25 04:30:16 0
DD3541
 
Resource Report
Resource Website
RRID:CVCL_9N23 Homo sapiens (Human) Karyotypic information: 46,XX,t(11;22)(23.3;q11.2)mat (ECACC=00050205)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:00050205,
Wikidata:Q54830794
CVCL_9N23 2026-07-25 04:30:16 0
DD3655
 
Resource Report
Resource Website
RRID:CVCL_9Q12 Homo sapiens (Human) Karyotypic information: 46,XX t(5;13)(p15.1;q32.3)pat (ECACC=01040309)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:01040309,
Wikidata:Q54830843
CVCL_9Q12 2026-07-25 04:30:17 0
DD3626
 
Resource Report
Resource Website
ECACC Cat# 01011711, RRID:CVCL_9N45 Homo sapiens (Human) Turner syndrome Karyotypic information: 46,X,del(Xq) (ECACC=01011711)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 01011711 ECACC:01011711,
Wikidata:Q54830835
CVCL_9N45 2026-07-25 04:30:17 0
DD3575
 
Resource Report
Resource Website
ECACC Cat# 00081509, RRID:CVCL_9Q01 Homo sapiens (Human) Karyotypic information: 47,XXX (ECACC=00081509)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 00081509 ECACC:00081509,
Wikidata:Q54830811
CVCL_9Q01 2026-07-25 04:30:16 0
DD3611
 
Resource Report
Resource Website
RRID:CVCL_9N41 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:00112921,
Wikidata:Q54830828
CVCL_9N41 2026-07-25 04:30:17 0
DD3626
 
Resource Report
Resource Website
RRID:CVCL_9N45 Homo sapiens (Human) Turner syndrome Karyotypic information: 46,X,del(Xq) (ECACC=01011711)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:01011711,
Wikidata:Q54830835
CVCL_9N45 2026-07-25 04:30:17 0
DD3590
 
Resource Report
Resource Website
RRID:CVCL_9Q04 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:00101217,
Wikidata:Q54830819
CVCL_9Q04 2026-07-25 04:30:17 0
DD3628
 
Resource Report
Resource Website
ECACC Cat# 01011713, RRID:CVCL_9Q10 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(q21.3) (ECACC=01011713)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 01011713 ECACC:01011713,
Wikidata:Q54830837
CVCL_9Q10 2026-07-25 04:30:17 0
DD3687
 
Resource Report
Resource Website
RRID:CVCL_9N55 Homo sapiens (Human) Karyotypic information: 46,XX.ish 22q11.2(cH748x2) (ECACC=01081516)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC:01081516,
Wikidata:Q54830860
CVCL_9N55 2026-07-25 04:30:18 0

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