FANCD2 (FA complementation group D2) - Rat Genome Database

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Gene: FANCD2 (FA complementation group D2) Homo sapiens
Analyze
Symbol: FANCD2
Name: FA complementation group D2
RGD ID: 1343234
HGNC Page HGNC
Description: Enables DNA polymerase binding activity. Involved in response to gamma radiation. Located in cytosol; nuclear body; and nucleolus. Implicated in Fanconi anemia; Fanconi anemia complementation group D2; and breast cancer. Biomarker of breast cancer and skin melanoma.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: DKFZp762A223; FA-D2; FA4; FACD; FAD; FAD2; FANCD; Fanconi anemia complementation group D2; Fanconi anemia group D2 protein; Fanconi anemia, complementation group D2; FLJ23826; type 4 Fanconi pancytopenia
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: FANCD2P1   FANCD2P2  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl310,026,370 - 10,101,932 (+)EnsemblGRCh38hg38GRCh38
GRCh38310,026,437 - 10,101,932 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37310,068,121 - 10,143,616 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36310,043,113 - 10,118,614 (+)NCBINCBI36hg18NCBI36
Build 34310,043,127 - 10,116,344NCBI
Celera310,003,566 - 10,079,281 (+)NCBI
Cytogenetic Map3p25.3NCBI
HuRef310,004,471 - 10,079,989 (+)NCBIHuRef
CHM1_1310,018,248 - 10,093,721 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dimethylhydrazine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17beta-estradiol  (EXP)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
4-Hydroxy-TEMPO  (ISO)
4-hydroxynon-2-enal  (ISO)
6-propyl-2-thiouracil  (ISO)
acetaldehyde  (EXP)
acetamide  (ISO)
acrolein  (EXP)
acrylamide  (ISO)
aflatoxin B1  (EXP,ISO)
Aflatoxin B2 alpha  (EXP)
alpha-pinene  (EXP)
antirheumatic drug  (EXP)
arsenous acid  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
bis(2-chloroethyl) sulfide  (EXP)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (EXP,ISO)
bortezomib  (EXP)
butanal  (EXP)
calcitriol  (EXP)
carbamazepine  (EXP)
carmustine  (EXP)
cefaloridine  (ISO)
chromium(6+)  (EXP)
cisplatin  (EXP)
coumestrol  (EXP)
crocidolite asbestos  (EXP)
curcumin  (EXP)
cyclosporin A  (EXP)
diarsenic trioxide  (EXP)
diepoxybutane  (EXP)
digitoxin  (EXP)
digoxin  (EXP)
dioxygen  (EXP)
doxorubicin  (EXP,ISO)
endosulfan  (EXP)
Enterolactone  (EXP)
enzyme inhibitor  (EXP)
erastin  (ISO)
ethanol  (EXP,ISO)
flutamide  (ISO)
folic acid  (EXP)
formaldehyde  (EXP)
furan  (ISO)
hydroxyurea  (EXP)
ivermectin  (EXP)
Lasiocarpine  (EXP)
lead(0)  (EXP)
lead(2+)  (EXP)
leflunomide  (EXP)
methotrexate  (EXP)
methylarsonic acid  (EXP)
mitomycin C  (EXP)
monocrotaline  (EXP)
N-Nitrosopyrrolidine  (EXP)
nickel dichloride  (EXP)
nitrogen mustard  (EXP)
ouabain  (EXP)
oxaliplatin  (ISO)
ozone  (EXP,ISO)
paracetamol  (EXP)
paraquat  (ISO)
PCB138  (ISO)
pentanal  (EXP)
phenethyl isothiocyanate  (EXP)
propanal  (EXP)
resveratrol  (EXP,ISO)
riddelliine  (EXP)
rotenone  (EXP)
SB 203580  (EXP)
senecionine  (ISO)
silicon dioxide  (EXP)
sodium arsenite  (EXP)
sunitinib  (EXP)
temozolomide  (EXP)
testosterone  (EXP)
thioacetamide  (ISO)
titanium dioxide  (ISO)
topotecan  (ISO)
trimellitic anhydride  (ISO)
triptonide  (ISO)
troglitazone  (EXP)
urethane  (EXP)
valproic acid  (EXP)
vinclozolin  (ISO)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Abnormal aortic morphology  (IAGP)
Abnormal aortic valve morphology  (IAGP)
Abnormal carotid artery morphology  (IAGP)
Abnormal heart morphology  (IAGP)
Abnormal localization of kidney  (IAGP)
Abnormal preputium morphology  (IAGP)
Abnormality of chromosome stability  (IAGP)
Abnormality of femur morphology  (IAGP)
Abnormality of the hypothalamus-pituitary axis  (IAGP)
Abnormality of the liver  (IAGP)
Absent radius  (IAGP)
Absent testis  (IAGP)
Absent thumb  (IAGP)
Aganglionic megacolon  (IAGP)
Agenesis of corpus callosum  (IAGP)
Almond-shaped palpebral fissure  (IAGP)
Anal atresia  (IAGP)
Anemia  (IAGP)
Anemic pallor  (IAGP)
Annular pancreas  (IAGP)
Aplasia of the 1st metacarpal  (IAGP)
Aplasia/Hypoplasia of fingers  (IAGP)
Aplasia/Hypoplasia of the iris  (IAGP)
Aplasia/Hypoplasia of the radius  (IAGP)
Aplasia/Hypoplasia of the uvula  (IAGP)
Arteriovenous malformation  (IAGP)
Astigmatism  (IAGP)
Atrial septal defect  (IAGP)
Attention deficit hyperactivity disorder  (IAGP)
Autosomal recessive inheritance  (IAGP)
Azoospermia  (IAGP)
Bicornuate uterus  (IAGP)
Blepharophimosis  (IAGP)
Bone marrow hypocellularity  (IAGP)
Breast carcinoma  (IAGP)
Bruising susceptibility  (IAGP)
Cafe-au-lait spot  (IAGP)
Cataract  (IAGP)
Choanal atresia  (IAGP)
Chromosomal breakage induced by crosslinking agents  (IAGP)
Cleft palate  (IAGP)
Clinodactyly of the 5th finger  (IAGP)
Clubbing of toes  (IAGP)
Complete duplication of thumb phalanx  (IAGP)
Cranial nerve paralysis  (IAGP)
Cryptorchidism  (IAGP)
Decreased fertility in males  (IAGP)
Deficient excision of UV-induced pyrimidine dimers in DNA  (IAGP)
Dolichocephaly  (IAGP)
Duodenal stenosis  (IAGP)
Duplicated collecting system  (IAGP)
Epicanthus  (IAGP)
Esophageal atresia  (IAGP)
External ear malformation  (IAGP)
Facial asymmetry  (IAGP)
Finger syndactyly  (IAGP)
Frontal bossing  (IAGP)
Global developmental delay  (IAGP)
Hearing impairment  (IAGP)
High palate  (IAGP)
Hip dislocation  (IAGP)
Horseshoe kidney  (IAGP)
Hydrocephalus  (IAGP)
Hydroureter  (IAGP)
Hypergonadotropic hypogonadism  (IAGP)
Hyperreflexia  (IAGP)
Hypertelorism  (IAGP)
Hypertrophic cardiomyopathy  (IAGP)
Hypogonadism  (IAGP)
Hypopigmented skin patches  (IAGP)
Hypoplasia of the corpus callosum  (IAGP)
Hypoplasia of the ulna  (IAGP)
Hypospadias  (IAGP)
Hypotelorism  (IAGP)
Intellectual disability  (IAGP)
Intrauterine growth retardation  (IAGP)
Leukemia  (IAGP)
Leukopenia  (IAGP)
Low-set ears  (IAGP)
Meckel diverticulum  (IAGP)
Microcephaly  (IAGP)
Micrognathia  (IAGP)
Micropenis  (IAGP)
Microphthalmia  (IAGP)
Multiple cafe-au-lait spots  (IAGP)
Myelodysplasia  (IAGP)
Neutropenia  (IAGP)
Nystagmus  (IAGP)
Oligohydramnios  (IAGP)
Pancytopenia  (IAGP)
Partial duplication of thumb phalanx  (IAGP)
Patent ductus arteriosus  (IAGP)
Pelvic kidney  (IAGP)
Pes planus  (IAGP)
Preaxial hand polydactyly  (IAGP)
Prolonged G2 phase of cell cycle  (IAGP)
Proptosis  (IAGP)
Ptosis  (IAGP)
Pyridoxine-responsive sideroblastic anemia  (IAGP)
Recurrent urinary tract infections  (IAGP)
Reduced bone mineral density  (IAGP)
Renal agenesis  (IAGP)
Renal duplication  (IAGP)
Renal hypoplasia/aplasia  (IAGP)
Renal insufficiency  (IAGP)
Reticulocytopenia  (IAGP)
Scoliosis  (IAGP)
Short palpebral fissure  (IAGP)
Short stature  (IAGP)
Short thumb  (IAGP)
Sloping forehead  (IAGP)
Small for gestational age  (IAGP)
Spina bifida  (IAGP)
Strabismus  (IAGP)
Tetralogy of Fallot  (IAGP)
Thrombocytopenia  (IAGP)
Toe syndactyly  (IAGP)
Tracheoesophageal fistula  (IAGP)
Triphalangeal thumb  (IAGP)
Umbilical hernia  (IAGP)
Upslanted palpebral fissure  (IAGP)
Ventriculomegaly  (IAGP)
Visual impairment  (IAGP)
Weight loss  (IAGP)
References

Additional References at PubMed
PMID:7581463   PMID:10762542   PMID:11239454   PMID:11733219   PMID:11751423   PMID:12042798   PMID:12086603   PMID:12093742   PMID:12239151   PMID:12389351   PMID:12447395   PMID:12477932  
PMID:12607003   PMID:12607005   PMID:12649160   PMID:12874027   PMID:12887909   PMID:12973351   PMID:14499622   PMID:14517836   PMID:14667412   PMID:14702039   PMID:14743216   PMID:14988723  
PMID:15115758   PMID:15199141   PMID:15257300   PMID:15302935   PMID:15314022   PMID:15377654   PMID:15454491   PMID:15489334   PMID:15502827   PMID:15650050   PMID:15661754   PMID:15671039  
PMID:15694335   PMID:15849361   PMID:15886296   PMID:16116422   PMID:16127171   PMID:16344560   PMID:16474167   PMID:16513431   PMID:16889989   PMID:16943440   PMID:17304220   PMID:17308347  
PMID:17314511   PMID:17333336   PMID:17436244   PMID:17460694   PMID:17643815   PMID:17898070   PMID:18029388   PMID:18082604   PMID:18212739   PMID:18263878   PMID:18270339   PMID:18469862  
PMID:18475298   PMID:18482162   PMID:18672388   PMID:18931676   PMID:18950845   PMID:19011769   PMID:19047177   PMID:19064571   PMID:19064572   PMID:19129235   PMID:19237606   PMID:19322201  
PMID:19423727   PMID:19465922   PMID:19466639   PMID:19504183   PMID:19536092   PMID:19536649   PMID:19561358   PMID:19609304   PMID:19671671   PMID:19690177   PMID:19704162   PMID:19714462  
PMID:19729998   PMID:19748364   PMID:19861535   PMID:19995904   PMID:20040763   PMID:20301575   PMID:20301753   PMID:20339950   PMID:20363922   PMID:20379614   PMID:20450923   PMID:20467437  
PMID:20496165   PMID:20507282   PMID:20519958   PMID:20538911   PMID:20556575   PMID:20603015   PMID:20603016   PMID:20603073   PMID:20671156   PMID:20676667   PMID:20805509   PMID:20819778  
PMID:20967207   PMID:21203397   PMID:21229326   PMID:21314979   PMID:21355096   PMID:21464321   PMID:21520247   PMID:21654808   PMID:21719678   PMID:21775430   PMID:21865299   PMID:21873635  
PMID:21912593   PMID:21919919   PMID:21995812   PMID:22258451   PMID:22293751   PMID:22484854   PMID:22705371   PMID:22828868   PMID:22829014   PMID:22854063   PMID:22855611   PMID:22863883  
PMID:22872141   PMID:22987153   PMID:23063585   PMID:23303816   PMID:23318456   PMID:23357080   PMID:23388460   PMID:23602568   PMID:23633493   PMID:23852546   PMID:23965832   PMID:23993743  
PMID:24005329   PMID:24036544   PMID:24036990   PMID:24104479   PMID:24278431   PMID:24451376   PMID:24512567   PMID:24556218   PMID:24623813   PMID:24658369   PMID:24708616   PMID:24755620  
PMID:24778252   PMID:24787670   PMID:24794430   PMID:24794434   PMID:24800743   PMID:24966277   PMID:25066130   PMID:25070891   PMID:25071006   PMID:25135477   PMID:25168188   PMID:25176410  
PMID:25319828   PMID:25489943   PMID:25542235   PMID:25557546   PMID:25652403   PMID:25659033   PMID:25736055   PMID:25801034   PMID:25862789   PMID:25891850   PMID:25893307   PMID:25921289  
PMID:26046368   PMID:26083937   PMID:26186194   PMID:26187992   PMID:26277624   PMID:26297932   PMID:26323318   PMID:26336824   PMID:26344197   PMID:26354767   PMID:26385482   PMID:26430909  
PMID:26496610   PMID:26584049   PMID:26625197   PMID:26687479   PMID:26765540   PMID:26980768   PMID:27097374   PMID:27114453   PMID:27264184   PMID:27277787   PMID:27322732   PMID:27373334  
PMID:27399778   PMID:27405460   PMID:27427384   PMID:27432908   PMID:27462463   PMID:27624129   PMID:27694619   PMID:27723720   PMID:27768874   PMID:27773793   PMID:27773819   PMID:27827420  
PMID:27880917   PMID:27977684   PMID:27986371   PMID:28157704   PMID:28162934   PMID:28196964   PMID:28314268   PMID:28330616   PMID:28386063   PMID:28514442   PMID:28575658   PMID:28628639  
PMID:28636932   PMID:28666371   PMID:28675297   PMID:28684355   PMID:28687786   PMID:28825622   PMID:29021208   PMID:29030393   PMID:29051491   PMID:29059323   PMID:29229926   PMID:29394375  
PMID:29463306   PMID:29556240   PMID:29656893   PMID:29760279   PMID:29937342   PMID:29955894   PMID:30154076   PMID:30176149   PMID:30335751   PMID:30431240   PMID:30456385   PMID:30804107  
PMID:30818369   PMID:30822218   PMID:30833792   PMID:30948266   PMID:31067464   PMID:31073040   PMID:31085681   PMID:31091453   PMID:31180492   PMID:31253762   PMID:31365120   PMID:31392348  
PMID:31586073   PMID:31628488   PMID:31633027   PMID:31745226   PMID:31753913   PMID:31980649   PMID:31980815   PMID:32062451   PMID:32092106   PMID:32167469   PMID:32269332   PMID:32398829  
PMID:32416067   PMID:32420600   PMID:32510829   PMID:32694731   PMID:32725171   PMID:32877691   PMID:32940045   PMID:33051438   PMID:33060197   PMID:33099537   PMID:33361032   PMID:33423298  
PMID:33514811   PMID:33795880   PMID:33845483   PMID:33961781   PMID:34079125   PMID:34256011  


Genomics

Comparative Map Data
FANCD2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl310,026,370 - 10,101,932 (+)EnsemblGRCh38hg38GRCh38
GRCh38310,026,437 - 10,101,932 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37310,068,121 - 10,143,616 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36310,043,113 - 10,118,614 (+)NCBINCBI36hg18NCBI36
Build 34310,043,127 - 10,116,344NCBI
Celera310,003,566 - 10,079,281 (+)NCBI
Cytogenetic Map3p25.3NCBI
HuRef310,004,471 - 10,079,989 (+)NCBIHuRef
CHM1_1310,018,248 - 10,093,721 (+)NCBICHM1_1
Fancd2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm396113,508,622 - 113,573,981 (+)NCBIGRCm39mm39
GRCm39 Ensembl6113,508,643 - 113,573,978 (+)Ensembl
GRCm386113,531,640 - 113,597,020 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl6113,531,682 - 113,597,017 (+)EnsemblGRCm38mm10GRCm38
MGSCv376113,481,676 - 113,546,279 (+)NCBIGRCm37mm9NCBIm37
MGSCv366113,497,462 - 113,562,062 (+)NCBImm8
Celera6115,358,610 - 115,423,076 (+)NCBICelera
Cytogenetic Map6E3NCBI
Fancd2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.24146,679,014 - 146,743,422 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl4146,679,179 - 146,743,412 (+)Ensembl
Rnor_6.04145,489,869 - 145,551,479 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl4145,489,869 - 145,551,479 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04208,784,762 - 208,848,203 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44149,424,558 - 149,500,006 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.14149,669,398 - 149,744,847 (+)NCBI
Celera4135,237,405 - 135,297,717 (+)NCBICelera
Cytogenetic Map4q42NCBI
Fancd2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555611,464,869 - 1,538,045 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049555611,460,080 - 1,538,026 (+)NCBIChiLan1.0ChiLan1.0
FANCD2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1310,310,243 - 10,389,229 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl310,312,476 - 10,389,190 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v039,932,292 - 10,037,332 (+)NCBIMhudiblu_PPA_v0panPan3
FANCD2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1208,240,270 - 8,297,269 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl208,240,311 - 8,297,568 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha208,273,907 - 8,330,979 (-)NCBI
ROS_Cfam_1.0208,269,549 - 8,326,574 (-)NCBI
UMICH_Zoey_3.1207,991,543 - 8,048,583 (-)NCBI
UNSW_CanFamBas_1.0208,337,151 - 8,394,193 (-)NCBI
UU_Cfam_GSD_1.0208,310,467 - 8,367,476 (-)NCBI
Fancd2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494215,689,153 - 15,747,539 (+)NCBI
SpeTri2.0NW_0049366023,162,177 - 3,220,468 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FANCD2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1366,241,673 - 66,310,436 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11366,241,951 - 66,308,601 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21373,314,050 - 73,380,806 (+)NCBISscrofa10.2Sscrofa10.2susScr3
FANCD2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12246,072,797 - 46,141,107 (+)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl2246,072,761 - 46,140,713 (+)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666041120,404,952 - 120,478,639 (-)NCBIVero_WHO_p1.0
Fancd2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247314,577,663 - 4,671,086 (+)NCBIHetGla_female_1.0hetGla2

Position Markers
SGC34603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37310,140,986 - 10,141,128UniSTSGRCh37
Build 36310,115,986 - 10,116,128RGDNCBI36
Celera310,076,653 - 10,076,795RGD
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p26UniSTS
HuRef310,077,361 - 10,077,503UniSTS
GeneMap99-GB4 RH Map349.44UniSTS
Whitehead-RH Map354.8UniSTS
RH92698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37310,140,756 - 10,140,924UniSTSGRCh37
Build 36310,115,756 - 10,115,924RGDNCBI36
Celera310,076,423 - 10,076,591RGD
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p26UniSTS
HuRef310,077,131 - 10,077,299UniSTS
GeneMap99-GB4 RH Map349.54UniSTS
D3S2947E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37310,067,790 - 10,067,889UniSTSGRCh37
Build 36310,042,790 - 10,042,889RGDNCBI36
Celera310,003,243 - 10,003,342RGD
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p26UniSTS
HuRef310,004,148 - 10,004,247UniSTS
SHGC-76726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37310,067,791 - 10,068,001UniSTSGRCh37
Build 36310,042,791 - 10,043,001RGDNCBI36
Celera310,003,244 - 10,003,454RGD
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p26UniSTS
HuRef310,004,149 - 10,004,359UniSTS
TNG Radiation Hybrid Map36054.0UniSTS
GeneMap99-GB4 RH Map356.59UniSTS
NCBI RH Map3132.9UniSTS
FANCD2_2498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37310,140,773 - 10,141,507UniSTSGRCh37
Build 36310,115,773 - 10,116,507RGDNCBI36
Celera310,076,440 - 10,077,174RGD
HuRef310,077,148 - 10,077,882UniSTS
SHGC-76704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37310,138,037 - 10,138,156UniSTSGRCh37
Build 36310,113,037 - 10,113,156RGDNCBI36
Celera310,073,704 - 10,073,823RGD
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p26UniSTS
HuRef310,074,412 - 10,074,531UniSTS
TNG Radiation Hybrid Map36007.0UniSTS
GeneMap99-GB4 RH Map349.54UniSTS
NCBI RH Map3132.9UniSTS
D8S2278  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p25.3-p24.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic MapXp22.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map12q14.3-q15UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q31UniSTS
D11S2921  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map10q24.33UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic MapXp11.4-p11.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map18pter-p11.3UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map7q21.12UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11p13-p12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map5q12-q13UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic MapXq25-q26.3UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map12p11.22UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map9p11UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map15q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q22-qterUniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19p13.2-cenUniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map9q33UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic MapXq26.2UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map5p13.1-p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map6q14.3-q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map6q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map6q11.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map14q11.2-q21UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map5p14.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map9p13.1UniSTS
Cytogenetic Map9q34.13UniSTS
D16S325  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map10q11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3q13.32UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map2p13-p12UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map8q21.13UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map1p36.3-p34.3UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19q13.4UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
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Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3226
Count of miRNA genes:1004
Interacting mature miRNAs:1198
Transcripts:ENST00000287647, ENST00000383806, ENST00000383807, ENST00000419585, ENST00000421731, ENST00000431693, ENST00000435522, ENST00000438741, ENST00000464934, ENST00000470028, ENST00000470757, ENST00000480909, ENST00000483276
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 180 12 46 35 822 39 263 50 102 63 590 235 8 3 2
Low 2209 2175 1418 364 1088 203 3384 1031 2359 295 859 1372 165 1197 2076 3
Below cutoff 50 801 260 223 41 222 709 1111 1266 61 8 5 2 1 7 709 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_007311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001018115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001319984 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001374253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001374254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001374255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_033084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC034193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF230336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF340183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH010533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK022613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074406 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC038666 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU617044 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX956311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA749163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA864640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA887207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ341263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000287647   ⟹   ENSP00000287647
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,026,414 - 10,099,660 (+)Ensembl
RefSeq Acc Id: ENST00000383807   ⟹   ENSP00000373318
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,026,429 - 10,101,930 (+)Ensembl
RefSeq Acc Id: ENST00000419585   ⟹   ENSP00000398754
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,026,499 - 10,101,930 (+)Ensembl
RefSeq Acc Id: ENST00000421731   ⟹   ENSP00000389936
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,049,462 - 10,101,926 (+)Ensembl
RefSeq Acc Id: ENST00000431693   ⟹   ENSP00000399354
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,028,620 - 10,041,562 (+)Ensembl
RefSeq Acc Id: ENST00000435522   ⟹   ENSP00000402166
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,026,468 - 10,034,513 (+)Ensembl
RefSeq Acc Id: ENST00000438741
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,034,707 - 10,040,684 (+)Ensembl
RefSeq Acc Id: ENST00000464934
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,046,427 - 10,049,504 (+)Ensembl
RefSeq Acc Id: ENST00000470028
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,093,288 - 10,101,282 (+)Ensembl
RefSeq Acc Id: ENST00000470757
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,064,355 - 10,072,978 (+)Ensembl
RefSeq Acc Id: ENST00000480909
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,064,693 - 10,072,964 (+)Ensembl
RefSeq Acc Id: ENST00000483276
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,045,527 - 10,048,059 (+)Ensembl
RefSeq Acc Id: ENST00000625535   ⟹   ENSP00000486945
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,028,658 - 10,032,351 (+)Ensembl
RefSeq Acc Id: ENST00000675286   ⟹   ENSP00000502379
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,026,437 - 10,101,932 (+)Ensembl
RefSeq Acc Id: ENST00000676013   ⟹   ENSP00000501999
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,026,417 - 10,101,261 (+)Ensembl
RefSeq Acc Id: ENST00000681997
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,045,527 - 10,099,009 (+)Ensembl
RefSeq Acc Id: ENST00000682647   ⟹   ENSP00000506736
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,026,370 - 10,063,935 (+)Ensembl
RefSeq Acc Id: ENST00000683263
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,045,596 - 10,099,009 (+)Ensembl
RefSeq Acc Id: ENST00000683312
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,092,737 - 10,098,993 (+)Ensembl
RefSeq Acc Id: ENST00000683933
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl310,081,085 - 10,096,365 (+)Ensembl
RefSeq Acc Id: NM_001018115   ⟹   NP_001018125
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38310,026,437 - 10,101,932 (+)NCBI
GRCh37310,068,113 - 10,143,614 (+)ENTREZGENE
Build 36310,043,113 - 10,118,614 (+)NCBI Archive
HuRef310,004,471 - 10,079,989 (+)ENTREZGENE
CHM1_1310,018,206 - 10,093,728 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001319984   ⟹   NP_001306913
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38310,026,437 - 10,101,932 (+)NCBI
CHM1_1310,018,287 - 10,093,728 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001374253   ⟹   NP_001361182
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38310,026,437 - 10,101,932 (+)NCBI
RefSeq Acc Id: NM_001374254   ⟹   NP_001361183
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38310,026,437 - 10,099,343 (+)NCBI
RefSeq Acc Id: NM_001374255   ⟹   NP_001361184
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38310,026,437 - 10,040,686 (+)NCBI
RefSeq Acc Id: NM_033084   ⟹   NP_149075
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38310,026,437 - 10,099,343 (+)NCBI
GRCh37310,068,113 - 10,143,614 (+)ENTREZGENE
Build 36310,043,113 - 10,116,344 (+)NCBI Archive
HuRef310,004,471 - 10,079,989 (+)ENTREZGENE
CHM1_1310,018,206 - 10,091,451 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001018125   ⟸   NM_001018115
- Peptide Label: isoform b
- UniProtKB: Q9BXW9 (UniProtKB/Swiss-Prot),   A0A024R2G2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_149075   ⟸   NM_033084
- Peptide Label: isoform a
- UniProtKB: Q9BXW9 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001306913   ⟸   NM_001319984
- Peptide Label: isoform b
- UniProtKB: Q9BXW9 (UniProtKB/Swiss-Prot),   A0A024R2G2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001361182   ⟸   NM_001374253
- Peptide Label: isoform c
RefSeq Acc Id: NP_001361183   ⟸   NM_001374254
- Peptide Label: isoform d
RefSeq Acc Id: NP_001361184   ⟸   NM_001374255
- Peptide Label: isoform e
RefSeq Acc Id: ENSP00000486945   ⟸   ENST00000625535
RefSeq Acc Id: ENSP00000398754   ⟸   ENST00000419585
RefSeq Acc Id: ENSP00000287647   ⟸   ENST00000287647
RefSeq Acc Id: ENSP00000399354   ⟸   ENST00000431693
RefSeq Acc Id: ENSP00000389936   ⟸   ENST00000421731
RefSeq Acc Id: ENSP00000402166   ⟸   ENST00000435522
RefSeq Acc Id: ENSP00000373318   ⟸   ENST00000383807
RefSeq Acc Id: ENSP00000502379   ⟸   ENST00000675286
RefSeq Acc Id: ENSP00000501999   ⟸   ENST00000676013
RefSeq Acc Id: ENSP00000506736   ⟸   ENST00000682647

Promoters
RGD ID:6863538
Promoter ID:EPDNEW_H4934
Type:initiation region
Name:FANCD2_1
Description:Fanconi anemia complementation group D2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38310,026,414 - 10,026,474EPDNEW
RGD ID:6800956
Promoter ID:HG_KWN:43682
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000383806,   NM_001018115,   OTTHUMT00000250562,   OTTHUMT00000339465,   OTTHUMT00000339622,   OTTHUMT00000339869,   OTTHUMT00000339870,   OTTHUMT00000339873,   OTTHUMT00000339876,   UC003BTO.1,   UC003BUS.2,   UC003BUV.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36310,042,886 - 10,043,797 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001018115.3(FANCD2):c.3888+314_3888+316del deletion not provided [RCV001564372] Chr3:10093635..10093637 [GRCh38]
Chr3:10135319..10135321 [GRCh37]
Chr3:3p25.3
likely benign
NM_001018115.3(FANCD2):c.3209A>T (p.His1070Leu) single nucleotide variant Fanconi anemia [RCV000550218]|Fanconi anemia, complementation group D2 [RCV001145540] Chr3:10081449 [GRCh38]
Chr3:10123133 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.1278+3_1278+5del deletion Fanconi anemia, complementation group D2 [RCV000600750]|not provided [RCV001573159] Chr3:10046726..10046728 [GRCh38]
Chr3:10088410..10088412 [GRCh37]
Chr3:3p25.3
benign|likely benign
NM_001018115.3(FANCD2):c.1470T>C (p.Asp490=) single nucleotide variant Fanconi anemia [RCV000526129] Chr3:10049430 [GRCh38]
Chr3:10091114 [GRCh37]
Chr3:3p25.3
likely benign
FANCD2, 376A-G insertion Fanconi anemia, complementation group D2 [RCV000012819] Chr3:3p25.3 pathogenic
FANCD2, EX17 DEL deletion Fanconi anemia, complementation group D2 [RCV000012822] Chr3:3p25.3 pathogenic
NM_001018115.3(FANCD2):c.4052C>T (p.Thr1351Met) single nucleotide variant Fanconi anemia [RCV000550015] Chr3:10096339 [GRCh38]
Chr3:10138023 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.1348A>G (p.Ile450Val) single nucleotide variant Fanconi anemia [RCV000552393]|Fanconi anemia, complementation group D2 [RCV000764453]|not provided [RCV001092962] Chr3:10047986 [GRCh38]
Chr3:10089670 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.672C>T (p.His224=) single nucleotide variant Fanconi anemia [RCV000528234]|Fanconi anemia, complementation group D2 [RCV001146796] Chr3:10039822 [GRCh38]
Chr3:10081506 [GRCh37]
Chr3:3p25.3
likely benign|uncertain significance
NM_033084.5(FANCD2):c.1759G>A (p.Ala587Thr) single nucleotide variant Fanconi anemia [RCV000529268] Chr3:10060396 [GRCh38]
Chr3:10102080 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.3707G>A (p.Arg1236His) single nucleotide variant Fanconi anemia, complementation group D2 [RCV000012818]|Inborn genetic diseases [RCV001265744] Chr3:10090315 [GRCh38]
Chr3:10131999 [GRCh37]
Chr3:3p25.3
pathogenic|uncertain significance
NM_001018115.3(FANCD2):c.904C>T (p.Arg302Trp) single nucleotide variant Fanconi anemia [RCV000809924]|Fanconi anemia, complementation group D2 [RCV000012820] Chr3:10043065 [GRCh38]
Chr3:10084749 [GRCh37]
Chr3:3p25.3
pathogenic|likely pathogenic
NM_001018115.3(FANCD2):c.958C>T (p.Gln320Ter) single nucleotide variant Fanconi anemia, complementation group D2 [RCV000012821] Chr3:10043119 [GRCh38]
Chr3:10084803 [GRCh37]
Chr3:3p25.3
pathogenic
GRCh38/hg38 3p25.3-25.2(chr3:8581778-12015238)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051480]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051480]|See cases [RCV000051480] Chr3:8581778..12015238 [GRCh38]
Chr3:8623464..12056738 [GRCh37]
Chr3:8598464..12031738 [NCBI36]
Chr3:3p25.3-25.2
pathogenic
GRCh38/hg38 3p25.3(chr3:9654297-10228687)x1 copy number loss See cases [RCV000051482] Chr3:9654297..10228687 [GRCh38]
Chr3:9695981..10270371 [GRCh37]
Chr3:9670981..10245371 [NCBI36]
Chr3:3p25.3
pathogenic
GRCh38/hg38 3p25.3-25.2(chr3:10019780-12251358)x1 copy number loss See cases [RCV000051506] Chr3:10019780..12251358 [GRCh38]
Chr3:10061464..12292857 [GRCh37]
Chr3:10036464..12267857 [NCBI36]
Chr3:3p25.3-25.2
pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:52266-11089569)x1 copy number loss See cases [RCV000051447] Chr3:52266..11089569 [GRCh38]
Chr3:93949..11131255 [GRCh37]
Chr3:68949..11106255 [NCBI36]
Chr3:3p26.3-25.3
pathogenic
GRCh38/hg38 3p26.3-22.2(chr3:52266-37148076)x3 copy number gain See cases [RCV000051097] Chr3:52266..37148076 [GRCh38]
Chr3:93949..37189567 [GRCh37]
Chr3:68949..37164571 [NCBI36]
Chr3:3p26.3-22.2
pathogenic
GRCh38/hg38 3p26.3-24.3(chr3:52066-20280127)x3 copy number gain See cases [RCV000051690] Chr3:52066..20280127 [GRCh38]
Chr3:93749..20321619 [GRCh37]
Chr3:68749..20296623 [NCBI36]
Chr3:3p26.3-24.3
pathogenic
GRCh38/hg38 3p26.3-24.1(chr3:52266-29248782)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051718]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051718]|See cases [RCV000051718] Chr3:52266..29248782 [GRCh38]
Chr3:93949..29290273 [GRCh37]
Chr3:68949..29265277 [NCBI36]
Chr3:3p26.3-24.1
pathogenic
GRCh38/hg38 3p26.3-24.3(chr3:63843-19510600)x3 copy number gain See cases [RCV000051719] Chr3:63843..19510600 [GRCh38]
Chr3:105526..19552092 [GRCh37]
Chr3:80526..19527096 [NCBI36]
Chr3:3p26.3-24.3
pathogenic
NM_001018115.3(FANCD2):c.983G>A (p.Arg328Gln) single nucleotide variant Fanconi anemia [RCV001084208]|Fanconi anemia, complementation group D2 [RCV001146799]|not provided [RCV000443739]|not specified [RCV000120984] Chr3:10043144 [GRCh38]
Chr3:10084828 [GRCh37]
Chr3:3p25.3
benign|likely benign|not provided
NM_001018115.3(FANCD2):c.1367T>G (p.Leu456Arg) single nucleotide variant Fanconi anemia [RCV000406228]|Fanconi anemia, complementation group D2 [RCV001094941]|not provided [RCV000434788]|not specified [RCV000120985] Chr3:10048005 [GRCh38]
Chr3:10089689 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity|not provided
NM_001018115.3(FANCD2):c.1634A>G (p.Asn545Ser) single nucleotide variant Fanconi anemia [RCV001084625]|Fanconi anemia, complementation group A [RCV000987100]|Fanconi anemia, complementation group D2 [RCV001146893]|not provided [RCV000422431]|not specified [RCV000120986] Chr3:10052475 [GRCh38]
Chr3:10094159 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity|not provided
NM_001018115.3(FANCD2):c.1777C>T (p.Pro593Ser) single nucleotide variant Fanconi anemia [RCV000459559]|Fanconi anemia, complementation group D2 [RCV000764454]|Malignant tumor of breast [RCV001004843]|not provided [RCV001541664]|not specified [RCV000120987] Chr3:10062161 [GRCh38]
Chr3:10103845 [GRCh37]
Chr3:3p25.3
uncertain significance|not provided
NM_001018115.3(FANCD2):c.1868A>C (p.Gln623Pro) single nucleotide variant Fanconi anemia [RCV000369483]|Fanconi anemia, complementation group A [RCV000987101]|Fanconi anemia, complementation group D2 [RCV001094843]|not provided [RCV001573401]|not specified [RCV000120988] Chr3:10063832 [GRCh38]
Chr3:10105516 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity|not provided
NM_001018115.3(FANCD2):c.2141C>T (p.Pro714Leu) single nucleotide variant Fanconi anemia [RCV000372215]|Fanconi anemia, complementation group A [RCV000987103]|Fanconi anemia, complementation group D2 [RCV001094876]|not provided [RCV001705892]|not specified [RCV000120989] Chr3:10064848 [GRCh38]
Chr3:10106532 [GRCh37]
Chr3:3p25.3
benign|not provided
NM_001018115.3(FANCD2):c.2555C>T (p.Pro852Leu) single nucleotide variant Fanconi anemia [RCV001034765]|not specified [RCV000120990] Chr3:10072931 [GRCh38]
Chr3:10114615 [GRCh37]
Chr3:3p25.3
uncertain significance|not provided
NM_001018115.3(FANCD2):c.2567C>G (p.Thr856Ser) single nucleotide variant not specified [RCV000120991] Chr3:10072943 [GRCh38]
Chr3:10114627 [GRCh37]
Chr3:3p25.3
not provided
NM_001018115.3(FANCD2):c.2702G>T (p.Gly901Val) single nucleotide variant Fanconi anemia [RCV000232207]|Fanconi anemia, complementation group D2 [RCV001094918]|not provided [RCV001567785]|not specified [RCV000120992] Chr3:10073349 [GRCh38]
Chr3:10115033 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity|not provided
NM_001018115.3(FANCD2):c.195G>C (p.Gln65His) single nucleotide variant Fanconi anemia [RCV000329799]|Fanconi anemia, complementation group D2 [RCV001094769]|not provided [RCV000431377]|not specified [RCV000120993] Chr3:10032962 [GRCh38]
Chr3:10074646 [GRCh37]
Chr3:3p25.3
benign|conflicting interpretations of pathogenicity|uncertain significance|not provided
NM_033084.5(FANCD2):c.2965C>G (p.Pro989Ala) single nucleotide variant Fanconi anemia [RCV000823688]|Fanconi anemia, complementation group D2 [RCV001145539]|not specified [RCV000120994] Chr3:10078186 [GRCh38]
Chr3:10119870 [GRCh37]
Chr3:3p25.3
uncertain significance|not provided
NM_001018115.3(FANCD2):c.2989C>T (p.Arg997Trp) single nucleotide variant Fanconi anemia [RCV001206909]|not specified [RCV000120995] Chr3:10081112 [GRCh38]
Chr3:10122796 [GRCh37]
Chr3:3p25.3
uncertain significance|not provided
NM_001018115.3(FANCD2):c.2990G>A (p.Arg997Gln) single nucleotide variant Fanconi anemia [RCV001308312]|not specified [RCV000120996] Chr3:10081113 [GRCh38]
Chr3:10122797 [GRCh37]
Chr3:3p25.3
uncertain significance|not provided
NM_173472.2(FANCD2OS):c.44-5667G>A single nucleotide variant not specified [RCV000120997] Chr3:10087198 [GRCh38]
Chr3:10128882 [GRCh37]
Chr3:3p25.3
not provided
NM_001018115.3(FANCD2):c.3446C>T (p.Ala1149Val) single nucleotide variant Fanconi anemia [RCV000299211]|Fanconi anemia, complementation group D2 [RCV001094805]|not provided [RCV000514928]|not specified [RCV000120998] Chr3:10087244 [GRCh38]
Chr3:10128928 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance|not provided
NM_173472.2(FANCD2OS):c.44-10680T>C single nucleotide variant not specified [RCV000120999] Chr3:10092211 [GRCh38]
Chr3:10133895 [GRCh37]
Chr3:3p25.3
not provided
NM_173472.2(FANCD2OS):c.43+2991A>C single nucleotide variant not specified [RCV000121000] Chr3:10101207 [GRCh38]
Chr3:10142891 [GRCh37]
Chr3:3p25.3
not provided
NM_001018115.3(FANCD2):c.516A>G (p.Ile172Met) single nucleotide variant Fanconi anemia [RCV000226716]|Fanconi anemia, complementation group D2 [RCV001094771]|not provided [RCV001572786]|not specified [RCV000121001] Chr3:10039303 [GRCh38]
Chr3:10080987 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity|not provided
NM_001018115.3(FANCD2):c.577A>G (p.Thr193Ala) single nucleotide variant Fanconi anemia [RCV000287066]|Fanconi anemia, complementation group D2 [RCV001094828]|not provided [RCV000224959]|not specified [RCV000121002] Chr3:10039727 [GRCh38]
Chr3:10081411 [GRCh37]
Chr3:3p25.3
pathogenic|benign|likely benign|conflicting interpretations of pathogenicity|not provided
NM_001018115.3(FANCD2):c.4281+115C>A single nucleotide variant Fanconi anemia [RCV000630963]|not specified [RCV000121003] Chr3:10098930 [GRCh38]
Chr3:10140614 [GRCh37]
Chr3:3p25.3
likely benign|not provided
GRCh38/hg38 3p25.3(chr3:9624696-10039318)x1 copy number loss See cases [RCV000133641] Chr3:9624696..10039318 [GRCh38]
Chr3:9666380..10081002 [GRCh37]
Chr3:9641380..10056002 [NCBI36]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.3513T>G (p.Asp1171Glu) single nucleotide variant Fanconi anemia, complementation group D2 [RCV001292987] Chr3:10088495 [GRCh38]
Chr3:10130179 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.1345A>G (p.Ser449Gly) single nucleotide variant Fanconi anemia, complementation group D2 [RCV001292638] Chr3:10047983 [GRCh38]
Chr3:10089667 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.3181T>C (p.Cys1061Arg) single nucleotide variant Fanconi anemia [RCV001303146] Chr3:10081421 [GRCh38]
Chr3:10123105 [GRCh37]
Chr3:3p25.3
uncertain significance
GRCh38/hg38 3p25.3(chr3:9896061-10220962)x1 copy number loss See cases [RCV000134249] Chr3:9896061..10220962 [GRCh38]
Chr3:9937745..10262646 [GRCh37]
Chr3:9912745..10237646 [NCBI36]
Chr3:3p25.3
pathogenic
GRCh38/hg38 3p26.1-25.3(chr3:8038727-11240931)x4 copy number gain See cases [RCV000135641] Chr3:8038727..11240931 [GRCh38]
Chr3:8080414..11282617 [GRCh37]
Chr3:8055414..11257617 [NCBI36]
Chr3:3p26.1-25.3
likely pathogenic
GRCh38/hg38 3p25.3-25.2(chr3:9394874-11690612)x1 copy number loss See cases [RCV000137433] Chr3:9394874..11690612 [GRCh38]
Chr3:9436558..11732086 [GRCh37]
Chr3:9411558..11707086 [NCBI36]
Chr3:3p25.3-25.2
pathogenic
GRCh38/hg38 3p26.1-25.2(chr3:7975734-12636917)x3 copy number gain See cases [RCV000137309] Chr3:7975734..12636917 [GRCh38]
Chr3:8017421..12678416 [GRCh37]
Chr3:7992421..12653416 [NCBI36]
Chr3:3p26.1-25.2
likely pathogenic
GRCh38/hg38 3p26.3-25.2(chr3:32241-12681483)x1 copy number loss See cases [RCV000138143] Chr3:32241..12681483 [GRCh38]
Chr3:73914..12722982 [GRCh37]
Chr3:48914..12697982 [NCBI36]
Chr3:3p26.3-25.2
pathogenic
GRCh38/hg38 3p26.3-24.1(chr3:32241-30064208)x3 copy number gain See cases [RCV000138004] Chr3:32241..30064208 [GRCh38]
Chr3:73914..30105699 [GRCh37]
Chr3:48914..30080703 [NCBI36]
Chr3:3p26.3-24.1
pathogenic
GRCh38/hg38 3p26.3-24.3(chr3:32241-20334387)x3 copy number gain See cases [RCV000137941] Chr3:32241..20334387 [GRCh38]
Chr3:73914..20375879 [GRCh37]
Chr3:48914..20350883 [NCBI36]
Chr3:3p26.3-24.3
pathogenic
GRCh38/hg38 3p25.3(chr3:9875909-10572677)x1 copy number loss See cases [RCV000137755] Chr3:9875909..10572677 [GRCh38]
Chr3:9917593..10614361 [GRCh37]
Chr3:9892593..10589361 [NCBI36]
Chr3:3p25.3
pathogenic
NM_001018115.3(FANCD2):c.2022-5C>T single nucleotide variant Fanconi anemia [RCV001434411]|Fanconi anemia, complementation group A [RCV000987102]|Fanconi anemia, complementation group D2 [RCV000368728]|not provided [RCV000860369]|not specified [RCV000202851] Chr3:10064724 [GRCh38]
Chr3:10106408 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
GRCh38/hg38 3p26.3-25.3(chr3:32241-11379835)x1 copy number loss See cases [RCV000138376] Chr3:32241..11379835 [GRCh38]
Chr3:73914..11421309 [GRCh37]
Chr3:48914..11396309 [NCBI36]
Chr3:3p26.3-25.3
pathogenic|likely benign
GRCh38/hg38 3p25.3(chr3:8941623-10151752)x3 copy number gain See cases [RCV000138535] Chr3:8941623..10151752 [GRCh38]
Chr3:8983307..10193436 [GRCh37]
Chr3:8958307..10168436 [NCBI36]
Chr3:3p25.3
likely benign|uncertain significance
GRCh38/hg38 3p26.3-25.1(chr3:32241-13613818)x3 copy number gain See cases [RCV000138946] Chr3:32241..13613818 [GRCh38]
Chr3:73914..13655318 [GRCh37]
Chr3:48914..13630319 [NCBI36]
Chr3:3p26.3-25.1
pathogenic
GRCh38/hg38 3p26.3-22.1(chr3:53308-41381521)x3 copy number gain See cases [RCV000141810] Chr3:53308..41381521 [GRCh38]
Chr3:94991..41423012 [GRCh37]
Chr3:69991..41398016 [NCBI36]
Chr3:3p26.3-22.1
pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:20213-11221602)x1 copy number loss See cases [RCV000141731] Chr3:20213..11221602 [GRCh38]
Chr3:61891..11263288 [GRCh37]
Chr3:36891..11238288 [NCBI36]
Chr3:3p26.3-25.3
pathogenic
NM_001018115.3(FANCD2):c.1278+3_1278+6del deletion not specified [RCV000203193] Chr3:10046723..10046726 [GRCh38]
Chr3:10088407..10088410 [GRCh37]
Chr3:3p25.3
uncertain significance
GRCh38/hg38 3p26.3-25.3(chr3:32241-10323124)x1 copy number loss See cases [RCV000143325] Chr3:32241..10323124 [GRCh38]
Chr3:73914..10364808 [GRCh37]
Chr3:48914..10339808 [NCBI36]
Chr3:3p26.3-25.3
pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:32241-10631310)x1 copy number loss See cases [RCV000143173] Chr3:32241..10631310 [GRCh38]
Chr3:73914..10672995 [GRCh37]
Chr3:48914..10647995 [NCBI36]
Chr3:3p26.3-25.3
pathogenic
GRCh38/hg38 3p26.1-25.1(chr3:7356110-14360442)x3 copy number gain See cases [RCV000143766] Chr3:7356110..14360442 [GRCh38]
Chr3:7397797..14401942 [GRCh37]
Chr3:7372797..14376946 [NCBI36]
Chr3:3p26.1-25.1
pathogenic
GRCh38/hg38 3p26.3-25.3(chr3:688897-11051142)x1 copy number loss See cases [RCV000143706] Chr3:688897..11051142 [GRCh38]
Chr3:730581..11092828 [GRCh37]
Chr3:705581..11067828 [NCBI36]
Chr3:3p26.3-25.3
pathogenic
GRCh37/hg19 3p25.3(chr3:9405337-10168892)x3 copy number gain See cases [RCV000240180] Chr3:9405337..10168892 [GRCh37]
Chr3:3p25.3
likely pathogenic
NM_001018115.3(FANCD2):c.382G>T (p.Gly128Cys) single nucleotide variant Fanconi anemia [RCV001317858]|Fanconi anemia, complementation group D2 [RCV000261784] Chr3:10035177 [GRCh38]
Chr3:10076861 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.2067C>T (p.Tyr689=) single nucleotide variant Fanconi anemia [RCV000262313]|Fanconi anemia, complementation group D2 [RCV001094844] Chr3:10064774 [GRCh38]
Chr3:10106458 [GRCh37]
Chr3:3p25.3
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001018115.3(FANCD2):c.1545+9T>C single nucleotide variant Fanconi anemia [RCV000265234]|Fanconi anemia, complementation group D2 [RCV001094781] Chr3:10049514 [GRCh38]
Chr3:10091198 [GRCh37]
Chr3:3p25.3
likely benign|conflicting interpretations of pathogenicity|uncertain significance
GRCh37/hg19 3p25.3-25.2(chr3:8922160-12338637)x1 copy number loss See cases [RCV000240139] Chr3:8922160..12338637 [GRCh37]
Chr3:3p25.3-25.2
pathogenic
NM_001018115.3(FANCD2):c.1413+3A>G single nucleotide variant Fanconi anemia, complementation group D2 [RCV000259684]|not provided [RCV001558356]|not specified [RCV000506372] Chr3:10048054 [GRCh38]
Chr3:10089738 [GRCh37]
Chr3:3p25.3
benign|likely benign
NM_001018115.3(FANCD2):c.2021+31C>T single nucleotide variant not provided [RCV001582684]|not specified [RCV000194494] Chr3:10064460 [GRCh38]
Chr3:10106144 [GRCh37]
Chr3:3p25.3
likely benign
NM_001018115.3(FANCD2):c.1947+69del deletion not specified [RCV000193257] Chr3:10063978 [GRCh38]
Chr3:10105662 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.2801C>G (p.Ser934Cys) single nucleotide variant Fanconi anemia [RCV001371615]|not specified [RCV000192337] Chr3:10074615 [GRCh38]
Chr3:10116299 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.2605+1G>A single nucleotide variant Fanconi anemia, complementation group D2 [RCV001332747]|not provided [RCV000255506] Chr3:10072982 [GRCh38]
Chr3:10114666 [GRCh37]
Chr3:3p25.3
likely pathogenic|uncertain significance
NM_001018115.3(FANCD2):c.2094CCT[1] (p.Leu700del) microsatellite Fanconi anemia, complementation group D2 [RCV000210268] Chr3:10064801..10064803 [GRCh38]
Chr3:10106485..10106487 [GRCh37]
Chr3:3p25.3
likely pathogenic
NM_001018115.3(FANCD2):c.2273G>C (p.Cys758Ser) single nucleotide variant Fanconi anemia [RCV000543810]|Fanconi anemia, complementation group D2 [RCV001292722] Chr3:10065867 [GRCh38]
Chr3:10107551 [GRCh37]
Chr3:3p25.3
likely benign|uncertain significance
NM_001018115.3(FANCD2):c.2555C>G (p.Pro852Arg) single nucleotide variant Fanconi anemia [RCV000228027]|Fanconi anemia, complementation group D2 [RCV001336827] Chr3:10072931 [GRCh38]
Chr3:10114615 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.2(FANCD2):c.378-14_378-13delTT deletion not provided [RCV000224506] Chr3:10035159..10035160 [GRCh38]
Chr3:10076843..10076844 [GRCh37]
Chr3:3p25.3
likely benign
NM_001018115.3(FANCD2):c.2148C>G (p.Thr716=) single nucleotide variant Fanconi anemia [RCV000230340]|Fanconi anemia, complementation group D2 [RCV001094877]|not specified [RCV001573813] Chr3:10064855 [GRCh38]
Chr3:10106539 [GRCh37]
Chr3:3p25.3
benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001018115.3(FANCD2):c.1414-9C>T single nucleotide variant Fanconi anemia [RCV000230800]|Fanconi anemia, complementation group D2 [RCV001094780]|not specified [RCV000249372] Chr3:10049365 [GRCh38]
Chr3:10091049 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity
NM_001018115.3(FANCD2):c.311T>C (p.Ile104Thr) single nucleotide variant Fanconi anemia [RCV000228749]|not specified [RCV000239243] Chr3:10034732 [GRCh38]
Chr3:10076416 [GRCh37]
Chr3:3p25.3
likely benign|uncertain significance
NM_001018115.3(FANCD2):c.986C>G (p.Ala329Gly) single nucleotide variant Fanconi anemia [RCV000232279]|not specified [RCV000238670] Chr3:10043147 [GRCh38]
Chr3:10084831 [GRCh37]
Chr3:3p25.3
likely pathogenic|likely benign|uncertain significance
NM_001018115.3(FANCD2):c.1156T>G (p.Phe386Val) single nucleotide variant Fanconi anemia [RCV000232848]|not specified [RCV000503335] Chr3:10046601 [GRCh38]
Chr3:10088285 [GRCh37]
Chr3:3p25.3
benign|uncertain significance
NM_001018115.3(FANCD2):c.4281+22_4281+29del deletion Fanconi anemia [RCV000231592] Chr3:10098837..10098844 [GRCh38]
Chr3:10140521..10140528 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.2937G>A (p.Met979Ile) single nucleotide variant Fanconi anemia [RCV000233936] Chr3:10078158 [GRCh38]
Chr3:10119842 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.2444G>A (p.Arg815Gln) single nucleotide variant Fanconi anemia [RCV000234321]|Fanconi anemia, complementation group D2 [RCV001194923] Chr3:10067267 [GRCh38]
Chr3:10108951 [GRCh37]
Chr3:3p25.3
pathogenic
NM_001018115.3(FANCD2):c.1311G>A (p.Ser437=) single nucleotide variant Fanconi anemia [RCV000227960] Chr3:10047949 [GRCh38]
Chr3:10089633 [GRCh37]
Chr3:3p25.3
likely benign
NM_001018115.3(FANCD2):c.1440T>C (p.His480=) single nucleotide variant Fanconi anemia [RCV000234648]|Fanconi anemia, complementation group D2 [RCV001144941]|not provided [RCV001557731] Chr3:10049400 [GRCh38]
Chr3:10091084 [GRCh37]
Chr3:3p25.3
likely benign|uncertain significance
NM_001018115.3(FANCD2):c.1810G>A (p.Asp604Asn) single nucleotide variant Fanconi anemia [RCV000227372] Chr3:10062194 [GRCh38]
Chr3:10103878 [GRCh37]
Chr3:3p25.3
uncertain significance
GRCh37/hg19 3p25.3(chr3:10128763-10188569)x1 copy number loss See cases [RCV000240014] Chr3:10128763..10188569 [GRCh37]
Chr3:3p25.3
pathogenic
NM_001018115.3(FANCD2):c.4281+543C>T single nucleotide variant Fanconi anemia, complementation group D2 [RCV000278448] Chr3:10099358 [GRCh38]
Chr3:10141042 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.1134+8T>G single nucleotide variant Fanconi anemia [RCV000283391]|Fanconi anemia, complementation group D2 [RCV001094849] Chr3:10043872 [GRCh38]
Chr3:10085556 [GRCh37]
Chr3:3p25.3
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001018115.3(FANCD2):c.2480A>C (p.Glu827Ala) single nucleotide variant Fanconi anemia [RCV001321654]|Fanconi anemia, complementation group D2 [RCV000283471] Chr3:10067303 [GRCh38]
Chr3:10108987 [GRCh37]
Chr3:3p25.3
uncertain significance
NM_001018115.3(FANCD2):c.1413+38A>C single nucleotide variant Fanconi anemia, complementation group D2 [RCV001701957]|not specified [RCV000248902] Chr3:10048089 [GRCh38]
Chr3:10089773 [GRCh37]
Chr3:3p25.3
benign
NM_018075.5(ANO10):c.1954A>G (p.Met652Val) single nucleotide variant Fanconi anemia, complementation group D2 [RCV001702381]|not provided [RCV001658191]|not specified [RCV000241778] Chr3:10065836 [GRCh38]
Chr3:10107520 [GRCh37]
Chr3:3p25.3
benign
NM_001018115.3(FANCD2):c.1414-8C>G single nucleotide variant not specified [RCV000244200] Chr3:10049366 [GRCh38]
Chr3:10091050 [GRCh37]
Chr3:3p25.3
likely benign
NM_001018115.3(FANCD2):c.1098+27A>G single nucleotide variant not specified [RCV000242015] Chr3:10043619 [GRCh38]
Chr3:10085303 [GRCh37]
Chr3:3p25.3
likely benign
NM_058195.4(CDKN2A):c.193+1G>A single nucleotide variant not provided [RCV001640501]|not specified [RCV000244460] Chr3:10096505 [GRCh38]
Chr3:10138189 [GRCh37]
Chr3:3p25.3
benign
NM_058195.4(CDKN2A):c.193+1G>A single nucleotide variant not provided [RCV001640497]|not specified [RCV000251855] Chr3:10101265 [GRCh38]
Chr3:10142949 [GRCh37]
Chr3:3p25.3
benign
NM_001018115.3(FANCD2):c.1509C>T (p.Asn503=) single nucleotide variant Fanconi anemia [RCV000466119]|Fanconi anemia, complementation group D2 [RCV001144943]|not provided [RCV001658190]|not specified [RCV000254141] Chr3:10049469 [GRCh38]
Chr3:10091153 [GRCh37]
Chr3:3p25.3
benign
NM_018075.5(ANO10):c.1954A>G (p.Met652Val) single nucleotide variant Fanconi anemia, complementation group D2 [RCV001702382]|not provided [RCV001640499]|not specified [RCV000247071] Chr3:10078233 [GRCh38]
Chr3:10119917 [GRCh37]
Chr3:3p25.3
benign
NM_001018115.3(FANCD2):c.1656+14T>A single nucleotide variant Fanconi anemia, complementation group D2 [RCV000380953]|not specified [RCV000249464] Chr3:10052511 [GRCh38]
Chr3:10094195 [GRCh37]
Chr3:3p25.3
likely benign|uncertain significance
NM_001018115.3(FANCD2):c.1336C>G (p.Leu446Val) single nucleotide variant Fanconi anemia [RCV000367310]|Fanconi anemia, complementation group D2 [RCV001094940]|not specified [RCV000251967] Chr3:10047974 [GRCh38]
Chr3:10089658 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001018115.3(FANCD2):c.2877A>G (p.Gln959=) single nucleotide variant Fanconi anemia [RCV000630974]|not specified [RCV000242304] Chr3:10078098 [GRCh38]
Chr3:10119782 [GRCh37]
Chr3:3p25.3
benign|likely benign
NM_001018115.3(FANCD2):c.1122A>G (p.Val374=) single nucleotide variant Fanconi anemia [RCV000377963]|Fanconi anemia, complementation group A [RCV000987095]|Fanconi anemia, complementation group D2 [RCV001094848]|not provided [RCV001706317]|not specified [RCV000247209] Chr3:10043852 [GRCh38]
Chr3:10085536 [GRCh37]
Chr3:3p25.3
benign
NM_018075.5(ANO10):c.1954A>G (p.Met652Val) single nucleotide variant Fanconi anemia, complementation group D2 [RCV001701809]|not provided [RCV001668451]|not specified [RCV000249626] Chr3:10036271 [GRCh38]
Chr3:10077955 [GRCh37]
Chr3:3p25.3
benign
NM_001018115.3(FANCD2):c.3560+42dup duplication not specified [RCV000252241] Chr3:10088578..10088579 [GRCh38]
Chr3:10130262..10130263 [GRCh37]
Chr3:3p25.3
likely benign
NM_139279.6(MCFD2):c.249del (p.Asp83fs) single nucleotide variant Fanconi anemia, complementation group D2 [RCV001701890]|not provided [RCV001636755]|not specified [RCV000245041] Chr3:10043446 [GRCh38]
Chr3:10085130 [GRCh37]
Chr3:3p25.3
benign
NM_001018115.3(FANCD2):c.3850-17G>T single nucleotide variant not specified [RCV000247493] Chr3:10093268 [GRCh38]
Chr3:10134952 [GRCh37]
Chr3:3p25.3
likely benign
NM_018075.5(ANO10):c.1954A>G (p.Met652Val) single nucleotide variant not provided [RCV001640498]|not specified [RCV000250034] Chr3:10065531 [GRCh38]
Chr3:10107215 [GRCh37]
Chr3:3p25.3
benign
NM_001018115.3(FANCD2):c.1414-23T>C single nucleotide variant not provided [RCV001675698]|not specified [RCV000252426] Chr3:10049351 [GRCh38]
Chr3:10091035 [GRCh37]
Chr3:3p25.3
benign
NM_144997.7(FLCN):c.1464G>A (p.Ala488=) single nucleotide variant Fanconi anemia, complementation group D2 [RCV000359625]|not provided [RCV001707579]|not specified [RCV000242722] Chr3:10092265 [GRCh38]
Chr3:10133949 [GRCh37]
Chr3:3p25.3
benign
NM_001018115.3(FANCD2):c.2712C>T (p.Asn904=) single nucleotide variant Fanconi anemia [RCV000344500]|Fanconi anemia, complementation group D2 [RCV001094919]|not provided [RCV001573849]|not specified [RCV000250137] Chr3:10073359 [GRCh38]
Chr3:10115043 [GRCh37]
Chr3:3p25.3
benign|likely benign|conflicting interpretations of pathogenicity
NM_058195.4(CDKN2A):c.193+1G>A single nucleotide variant Fanconi anemia [RCV001517145]|Fanconi anemia, complementation group D2 [RCV000264931]|not provided [RCV001640500]|not specified [RCV000252662] Chr3:10096385 [GRCh38]
Chr3:10138069 [GRCh37]
Chr3:3p25.3
benign
NM_018075.5(ANO10):c.1954A>G (p.Met652Val) single nucleotide variant not provided [RCV001658192]|not specified [RCV000252762] Chr3:10039690 [GRCh38]
Chr3:10081374 [GRCh37]
Chr3:3p25.3
benign
NM_139279.6(MCFD2):c.249del (p.Asp83fs) single nucleotide variant Fanconi anemia, complementation group D2 [RCV001701888]|not provided [RCV001618399]|not specified [RCV000248075] Chr3:10039861 [GRCh38]
Chr3:10081545 [GRCh37]
Chr3:3p25.3
benign
NM_001018115.3(FANCD2):c.64+12G>C