WDR62 (WD repeat domain 62) - Rat Genome Database
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Gene: WDR62 (WD repeat domain 62) Homo sapiens
Analyze
Symbol: WDR62
Name: WD repeat domain 62
RGD ID: 1315489
HGNC Page HGNC
Description: Involved in microtubule cytoskeleton organization and nervous system development. Localizes to cytosol; microtubule cytoskeleton; and nucleus. Implicated in intellectual disability; primary autosomal recessive microcephaly; and primary autosomal recessive microcephaly 2 with or without cortical malformations.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: C19orf14; DKFZp434J046; DKFZp686G1024; FLJ33298; MCPH2; MGC166976; microcephaly, primary autosomal recessive 2; truncated WDR62; WD repeat-containing protein 62
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1936,054,649 - 36,105,108 (+)EnsemblGRCh38hg38GRCh38
GRCh38.p13 Ensembl1936,054,881 - 36,105,108 (+)EnsemblGRCh38hg38GRCh38
GRCh381936,054,881 - 36,111,145 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371936,545,799 - 36,596,010 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361941,237,623 - 41,287,852 (+)NCBINCBI36hg18NCBI36
Celera1933,259,959 - 33,310,190 (+)NCBI
Cytogenetic Map19q13.12NCBI
HuRef1933,051,308 - 33,101,495 (+)NCBIHuRef
CHM1_11936,547,139 - 36,597,353 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
centriolar satellite  (IDA)
centriole  (IEA)
centrosome  (IDA)
cytosol  (IDA)
nucleus  (IBA,IDA)
spindle pole  (IBA,IDA)

Molecular Function

References

Additional References at PubMed
PMID:8889548   PMID:10573015   PMID:12477932   PMID:14702039   PMID:15057824   PMID:15302935   PMID:15489334   PMID:16169070   PMID:16189514   PMID:16565220   PMID:17081983   PMID:19910486  
PMID:20301772   PMID:20360068   PMID:20562859   PMID:20729831   PMID:20890278   PMID:20890279   PMID:20980985   PMID:21749326   PMID:21873635   PMID:23065275   PMID:23341463   PMID:23602568  
PMID:23920402   PMID:24228726   PMID:24255178   PMID:24388750   PMID:24842779   PMID:25385192   PMID:25416956   PMID:25476789   PMID:25515538   PMID:26186194   PMID:26297806   PMID:26472760  
PMID:26496610   PMID:26638075   PMID:26871637   PMID:26972000   PMID:27026702   PMID:27107014   PMID:27173435   PMID:27784895   PMID:27852057   PMID:28089251   PMID:28272472   PMID:28277612  
PMID:28377545   PMID:28514442   PMID:28700943   PMID:28718761   PMID:28756000   PMID:28973348   PMID:29395067   PMID:29568061   PMID:30021525   PMID:30091641   PMID:30102701   PMID:30706430  
PMID:30884127   PMID:30942440   PMID:30945288   PMID:31024071   PMID:31091453   PMID:31197141   PMID:31586073   PMID:31617661   PMID:31753913   PMID:32129710   PMID:32296183   PMID:32877691  


Genomics

Comparative Map Data
WDR62
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1936,054,649 - 36,105,108 (+)EnsemblGRCh38hg38GRCh38
GRCh38.p13 Ensembl1936,054,881 - 36,105,108 (+)EnsemblGRCh38hg38GRCh38
GRCh381936,054,881 - 36,111,145 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371936,545,799 - 36,596,010 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361941,237,623 - 41,287,852 (+)NCBINCBI36hg18NCBI36
Celera1933,259,959 - 33,310,190 (+)NCBI
Cytogenetic Map19q13.12NCBI
HuRef1933,051,308 - 33,101,495 (+)NCBIHuRef
CHM1_11936,547,139 - 36,597,353 (+)NCBICHM1_1
Wdr62
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39729,939,563 - 29,980,243 (-)NCBIGRCm39mm39
GRCm39 Ensembl729,939,563 - 29,979,844 (-)Ensembl
GRCm38730,240,138 - 30,281,908 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl730,240,138 - 30,280,419 (-)EnsemblGRCm38mm10GRCm38
MGSCv37731,025,157 - 31,065,440 (-)NCBIGRCm37mm9NCBIm37
MGSCv36729,948,898 - 29,989,181 (-)NCBImm8
Celera724,846,534 - 24,911,761 (-)NCBICelera
Cytogenetic Map7B1NCBI
Wdr62
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2185,491,531 - 85,530,643 (-)NCBI
Rnor_6.0 Ensembl188,694,824 - 88,734,223 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0190,995,545 - 91,034,592 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0192,132,727 - 92,171,774 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4185,448,728 - 85,482,510 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1185,526,838 - 85,560,621 (+)NCBI
Celera179,865,970 - 79,905,079 (-)NCBICelera
Cytogenetic Map1q21NCBI
Wdr62
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554682,503,885 - 2,545,255 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554682,504,181 - 2,545,982 (-)NCBIChiLan1.0ChiLan1.0
WDR62
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11941,721,289 - 41,777,038 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1941,721,281 - 41,777,038 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01932,973,725 - 33,030,297 (+)NCBIMhudiblu_PPA_v0panPan3
WDR62
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11116,594,243 - 116,641,206 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1116,594,244 - 116,641,191 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1115,999,825 - 116,047,171 (-)NCBI
ROS_Cfam_1.01117,197,202 - 117,244,720 (-)NCBI
UMICH_Zoey_3.11116,764,609 - 116,811,924 (-)NCBI
UNSW_CanFamBas_1.01116,384,790 - 116,432,353 (-)NCBI
UU_Cfam_GSD_1.01117,439,956 - 117,487,492 (-)NCBI
Wdr62
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_ltri_2NW_02440934911,309,957 - 11,349,593 (+)NCBI
SpeTri2.0NW_00493692280,136 - 119,702 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
WDR62
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl645,419,041 - 45,474,050 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1645,418,966 - 45,477,619 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2640,820,975 - 40,876,258 (+)NCBISscrofa10.2Sscrofa10.2susScr3
WDR62
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1630,964,219 - 31,010,692 (+)NCBI
ChlSab1.1 Ensembl630,964,319 - 31,011,403 (+)Ensembl
Wdr62
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462479410,309,855 - 10,358,018 (+)NCBI

Position Markers
D19S416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371934,068,650 - 34,068,814UniSTSGRCh37
Build 361938,760,490 - 38,760,654RGDNCBI36
Celera1930,762,272 - 30,762,442RGD
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map19q13.32UniSTS
HuRef1930,568,303 - 30,568,474UniSTS
Marshfield Genetic Map1958.69UniSTS
Marshfield Genetic Map1958.69RGD
Genethon Genetic Map1958.1UniSTS
deCODE Assembly Map1956.7UniSTS
Whitehead-YAC Contig Map19 UniSTS
D19S420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371943,808,799 - 43,809,061UniSTSGRCh37
Build 361948,500,639 - 48,500,901RGDNCBI36
Celera1940,609,340 - 40,609,604RGD
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.2UniSTS
HuRef1940,238,475 - 40,238,739UniSTS
Marshfield Genetic Map1966.3UniSTS
Marshfield Genetic Map1966.3RGD
Genethon Genetic Map1966.0UniSTS
deCODE Assembly Map1968.94UniSTS
Whitehead-RH Map19324.0UniSTS
Whitehead-YAC Contig Map19 UniSTS
NCBI RH Map19470.1UniSTS
SHGC-23212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371936,587,643 - 36,587,785UniSTSGRCh37
Build 361941,279,483 - 41,279,625RGDNCBI36
Celera1933,301,822 - 33,301,964RGD
Cytogenetic Map19q13.12UniSTS
HuRef1933,093,127 - 33,093,269UniSTS
TNG Radiation Hybrid Map1913094.0UniSTS
Stanford-G3 RH Map191545.0UniSTS
D10S16   No map positions available.
L30021  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map2q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map6q21UniSTS
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
D1S1423  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p22.3-p21.32UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map9q12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map10p14-p13UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map11q23-q24UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map22cen-q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map4q28UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map1q41-q42UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map11q24.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3q13UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map9p21.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq27.2UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map20q11.21-q11.23UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map15q26UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p15.1-p14UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map7q32.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21-q24UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map8q24.12UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map6q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map20pter-p12UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map14q22.2UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p22-p21UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map10q22.3-q23.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map3p12.3UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map3q11.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6p24.2UniSTS
Cytogenetic Map20q13.33UniSTS
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
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
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
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4424
Count of miRNA genes:1157
Interacting mature miRNAs:1470
Transcripts:ENST00000270301, ENST00000378860, ENST00000388999, ENST00000401500, ENST00000427823, ENST00000587391, ENST00000589953, ENST00000608676
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
High
Medium 80 96 26 23 326 23 439 313 86 38 535 201 9 196
Low 1326 1768 1316 332 1293 209 3285 1217 2204 187 823 1371 129 851 2053 5
Below cutoff 1031 1124 383 267 332 233 632 666 1436 193 99 39 35 1 353 539

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_028101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001083961 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_173636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005258809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526837 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526838 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526840 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526841 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526844 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001753671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001753672 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC004144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AD000813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK090617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL041673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL117438 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL133651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW029580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC017261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC058939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC128417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC151839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ880028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ960310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU508347 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647726 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CF142643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT070565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178897 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178898 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178899 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000270301   ⟹   ENSP00000270301
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,972 - 36,105,103 (+)Ensembl
RefSeq Acc Id: ENST00000378860
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,881 - 36,074,304 (+)Ensembl
RefSeq Acc Id: ENST00000401500   ⟹   ENSP00000384792
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,897 - 36,105,108 (+)Ensembl
RefSeq Acc Id: ENST00000427823   ⟹   ENSP00000413475
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,990 - 36,071,562 (+)Ensembl
RefSeq Acc Id: ENST00000587391   ⟹   ENSP00000465525
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,963 - 36,105,106 (+)Ensembl
RefSeq Acc Id: ENST00000589953
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,071,606 - 36,075,417 (+)Ensembl
RefSeq Acc Id: ENST00000608676
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,963 - 36,062,649 (+)Ensembl
RefSeq Acc Id: ENST00000644764   ⟹   ENSP00000494253
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,058,804 - 36,084,737 (+)Ensembl
RefSeq Acc Id: ENST00000679357   ⟹   ENSP00000506376
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,092,689 - 36,105,034 (+)Ensembl
RefSeq Acc Id: ENST00000679422   ⟹   ENSP00000505316
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,092,689 - 36,102,151 (+)Ensembl
RefSeq Acc Id: ENST00000679489   ⟹   ENSP00000505399
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,086,687 - 36,091,311 (+)Ensembl
RefSeq Acc Id: ENST00000679598   ⟹   ENSP00000504936
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,102,752 - 36,105,108 (+)Ensembl
RefSeq Acc Id: ENST00000679682   ⟹   ENSP00000506226
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,897 - 36,105,098 (+)Ensembl
RefSeq Acc Id: ENST00000679714   ⟹   ENSP00000506627
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,897 - 36,105,095 (+)Ensembl
RefSeq Acc Id: ENST00000679757   ⟹   ENSP00000505158
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,930 - 36,105,104 (+)Ensembl
RefSeq Acc Id: ENST00000679858   ⟹   ENSP00000505655
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,946 - 36,105,108 (+)Ensembl
RefSeq Acc Id: ENST00000680211   ⟹   ENSP00000506102
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,100,595 - 36,105,108 (+)Ensembl
RefSeq Acc Id: ENST00000680280
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,102,230 - 36,104,975 (+)Ensembl
RefSeq Acc Id: ENST00000680321   ⟹   ENSP00000505525
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,897 - 36,075,420 (+)Ensembl
RefSeq Acc Id: ENST00000680349
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,090,504 - 36,105,105 (+)Ensembl
RefSeq Acc Id: ENST00000680359   ⟹   ENSP00000506079
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,897 - 36,086,914 (+)Ensembl
RefSeq Acc Id: ENST00000680377   ⟹   ENSP00000505055
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,084,653 - 36,099,617 (+)Ensembl
RefSeq Acc Id: ENST00000680403   ⟹   ENSP00000505677
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,897 - 36,104,931 (+)Ensembl
RefSeq Acc Id: ENST00000680489
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,649 - 36,093,142 (+)Ensembl
RefSeq Acc Id: ENST00000680564   ⟹   ENSP00000505582
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,897 - 36,105,108 (+)Ensembl
RefSeq Acc Id: ENST00000680590   ⟹   ENSP00000505350
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,897 - 36,105,108 (+)Ensembl
RefSeq Acc Id: ENST00000680597   ⟹   ENSP00000505037
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,102,752 - 36,105,108 (+)Ensembl
RefSeq Acc Id: ENST00000680739   ⟹   ENSP00000505170
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,102,014 - 36,105,108 (+)Ensembl
RefSeq Acc Id: ENST00000680773
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,100,332 - 36,105,092 (+)Ensembl
RefSeq Acc Id: ENST00000680806   ⟹   ENSP00000506418
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,940 - 36,105,002 (+)Ensembl
RefSeq Acc Id: ENST00000680858   ⟹   ENSP00000505451
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,084,653 - 36,099,617 (+)Ensembl
RefSeq Acc Id: ENST00000680997
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,101,346 - 36,105,069 (+)Ensembl
RefSeq Acc Id: ENST00000681088   ⟹   ENSP00000504920
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,092,689 - 36,102,151 (+)Ensembl
RefSeq Acc Id: ENST00000681302   ⟹   ENSP00000505966
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,084,653 - 36,099,617 (+)Ensembl
RefSeq Acc Id: ENST00000681542   ⟹   ENSP00000505251
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,897 - 36,075,418 (+)Ensembl
RefSeq Acc Id: ENST00000681597
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,066,047 - 36,067,565 (+)Ensembl
RefSeq Acc Id: ENST00000681608
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,101,745 - 36,105,067 (+)Ensembl
RefSeq Acc Id: ENST00000681625   ⟹   ENSP00000505555
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,962 - 36,105,075 (+)Ensembl
RefSeq Acc Id: ENST00000681648
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,102,218 - 36,105,077 (+)Ensembl
RefSeq Acc Id: ENST00000681809   ⟹   ENSP00000505740
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1936,054,921 - 36,071,716 (+)Ensembl
RefSeq Acc Id: NM_001083961   ⟹   NP_001077430
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,897 - 36,105,108 (+)NCBI
GRCh371936,545,783 - 36,596,012 (+)NCBI
Build 361941,237,623 - 41,287,852 (+)NCBI Archive
HuRef1933,051,308 - 33,101,495 (+)ENTREZGENE
CHM1_11936,547,139 - 36,597,353 (+)NCBI
Sequence:
RefSeq Acc Id: NM_173636   ⟹   NP_775907
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,897 - 36,105,108 (+)NCBI
GRCh371936,545,783 - 36,596,012 (+)ENTREZGENE
Build 361941,237,623 - 41,287,852 (+)NCBI Archive
HuRef1933,051,308 - 33,101,495 (+)ENTREZGENE
CHM1_11936,547,139 - 36,597,353 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005258809   ⟹   XP_005258866
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,881 - 36,105,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526837   ⟹   XP_011525139
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,881 - 36,105,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526838   ⟹   XP_011525140
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,881 - 36,105,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526839   ⟹   XP_011525141
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,881 - 36,105,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526840   ⟹   XP_011525142
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,073,364 - 36,105,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526841   ⟹   XP_011525143
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,081,858 - 36,105,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526842   ⟹   XP_011525144
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,083,100 - 36,105,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526843   ⟹   XP_011525145
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,090,445 - 36,105,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526844   ⟹   XP_011525146
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,091,239 - 36,105,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017026665   ⟹   XP_016882154
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,881 - 36,111,145 (+)NCBI
Sequence:
RefSeq Acc Id: XR_001753671
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,881 - 36,094,118 (+)NCBI
Sequence:
RefSeq Acc Id: XR_001753672
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,881 - 36,094,118 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001077430   ⟸   NM_001083961
- Peptide Label: isoform 1
- UniProtKB: O43379 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_775907   ⟸   NM_173636
- Peptide Label: isoform 2
- UniProtKB: O43379 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005258866   ⟸   XM_005258809
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011525140   ⟸   XM_011526838
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011525139   ⟸   XM_011526837
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011525141   ⟸   XM_011526839
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011525142   ⟸   XM_011526840
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_011525143   ⟸   XM_011526841
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_011525144   ⟸   XM_011526842
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_011525145   ⟸   XM_011526843
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_011525146   ⟸   XM_011526844
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_016882154   ⟸   XM_017026665
- Peptide Label: isoform X1
- UniProtKB: O43379 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000413475   ⟸   ENST00000427823
RefSeq Acc Id: ENSP00000384792   ⟸   ENST00000401500
RefSeq Acc Id: ENSP00000270301   ⟸   ENST00000270301
RefSeq Acc Id: ENSP00000465525   ⟸   ENST00000587391
RefSeq Acc Id: ENSP00000494253   ⟸   ENST00000644764
RefSeq Acc Id: ENSP00000505966   ⟸   ENST00000681302
RefSeq Acc Id: ENSP00000505037   ⟸   ENST00000680597
RefSeq Acc Id: ENSP00000505740   ⟸   ENST00000681809
RefSeq Acc Id: ENSP00000505170   ⟸   ENST00000680739
RefSeq Acc Id: ENSP00000505055   ⟸   ENST00000680377
RefSeq Acc Id: ENSP00000505451   ⟸   ENST00000680858
RefSeq Acc Id: ENSP00000505316   ⟸   ENST00000679422
RefSeq Acc Id: ENSP00000505555   ⟸   ENST00000681625
RefSeq Acc Id: ENSP00000505251   ⟸   ENST00000681542
RefSeq Acc Id: ENSP00000505655   ⟸   ENST00000679858
RefSeq Acc Id: ENSP00000505525   ⟸   ENST00000680321
RefSeq Acc Id: ENSP00000506102   ⟸   ENST00000680211
RefSeq Acc Id: ENSP00000505677   ⟸   ENST00000680403
RefSeq Acc Id: ENSP00000505350   ⟸   ENST00000680590
RefSeq Acc Id: ENSP00000506079   ⟸   ENST00000680359
RefSeq Acc Id: ENSP00000506376   ⟸   ENST00000679357
RefSeq Acc Id: ENSP00000506418   ⟸   ENST00000680806
RefSeq Acc Id: ENSP00000505582   ⟸   ENST00000680564
RefSeq Acc Id: ENSP00000506627   ⟸   ENST00000679714
RefSeq Acc Id: ENSP00000504936   ⟸   ENST00000679598
RefSeq Acc Id: ENSP00000506226   ⟸   ENST00000679682
RefSeq Acc Id: ENSP00000505158   ⟸   ENST00000679757
RefSeq Acc Id: ENSP00000504920   ⟸   ENST00000681088
RefSeq Acc Id: ENSP00000505399   ⟸   ENST00000679489
Protein Domains
WD_REPEATS_REGION

Promoters
RGD ID:7239637
Promoter ID:EPDNEW_H25564
Type:initiation region
Name:WDR62_1
Description:WD repeat domain 62
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H25560  EPDNEW_H25565  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,054,913 - 36,054,973EPDNEW
RGD ID:7239639
Promoter ID:EPDNEW_H25565
Type:initiation region
Name:WDR62_2
Description:WD repeat domain 62
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H25560  EPDNEW_H25564  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381936,055,057 - 36,055,117EPDNEW
RGD ID:6795397
Promoter ID:HG_KWN:29708
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:ENST00000388999,   ENST00000392182,   NM_001083961,   NM_152658,   NM_173636,   OTTHUMT00000109534,   UC002ODB.2,   UC010EER.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361941,236,846 - 41,237,802 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001083961.2(WDR62):c.875A>C (p.Asn292Thr) single nucleotide variant not provided [RCV000521990] Chr19:36068003 [GRCh38]
Chr19:36558905 [GRCh37]
Chr19:19q13.12
conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.3361del (p.Ala1121fs) deletion Intellectual disability [RCV001291203] Chr19:36102971 [GRCh38]
Chr19:36593873 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.2086del (p.Ser696fs) deletion Primary autosomal recessive microcephaly 2 [RCV000024035] Chr19:36091248 [GRCh38]
Chr19:36582150 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.2742_2743AG[2] (p.Gln918fs) microsatellite Primary autosomal recessive microcephaly 2 [RCV000024036] Chr19:36100750..36100751 [GRCh38]
Chr19:36591652..36591653 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.4205_4208del (p.Val1402fs) deletion Primary autosomal recessive microcephaly 2 [RCV000000057] Chr19:36104569..36104572 [GRCh38]
Chr19:36595471..36595474 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.3839_3855del (p.Gly1280fs) deletion Primary autosomal recessive microcephaly 2 [RCV000000061] Chr19:36103666..36103682 [GRCh38]
Chr19:36594568..36594584 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.1598A>G (p.His533Arg) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001291523] Chr19:36084700 [GRCh38]
Chr19:36575602 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3294T>C (p.Ser1098=) single nucleotide variant not provided [RCV000728018] Chr19:36102810 [GRCh38]
Chr19:36593712 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1313G>A (p.Arg438His) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000024029] Chr19:36081512 [GRCh38]
Chr19:36572414 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.4241dup (p.Ser1415fs) duplication Primary autosomal recessive microcephaly 2 [RCV000024030] Chr19:36104604..36104605 [GRCh38]
Chr19:36595506..36595507 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.1531G>A (p.Asp511Asn) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000024031]|Primary microcephaly type 2 [RCV001250231] Chr19:36083222 [GRCh38]
Chr19:36574124 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.3936dup (p.Val1313fs) duplication Primary autosomal recessive microcephaly 2 [RCV000024032] Chr19:36103758..36103759 [GRCh38]
Chr19:36594660..36594661 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.363del (p.Asp122fs) deletion Primary autosomal recessive microcephaly 2 [RCV000024033] Chr19:36065988 [GRCh38]
Chr19:36556890 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.193G>A (p.Val65Met) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000024034] Chr19:36058795 [GRCh38]
Chr19:36549697 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.1576G>A (p.Glu526Lys) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000000058]|Primary autosomal recessive microcephaly [RCV001174806]|not provided [RCV000489330] Chr19:36084678 [GRCh38]
Chr19:36575580 [GRCh37]
Chr19:19q13.12
pathogenic|likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance|conflicting data from submitters
NM_001083961.2(WDR62):c.671G>C (p.Trp224Ser) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000000059] Chr19:36067415 [GRCh38]
Chr19:36558317 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.1408C>T (p.Gln470Ter) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000000060] Chr19:36083099 [GRCh38]
Chr19:36574001 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.1(WDR62):c.1716G>A (p.Leu572=) single nucleotide variant Malignant melanoma [RCV000072101] Chr19:36086760 [GRCh38]
Chr19:36577662 [GRCh37]
Chr19:41269502 [NCBI36]
Chr19:19q13.12
not provided
NM_001083961.2(WDR62):c.142C>T (p.Leu48Phe) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000600097]|not provided [RCV000224079]|not specified [RCV000079451] Chr19:36055113 [GRCh38]
Chr19:36546015 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.156C>G (p.Ser52=) single nucleotide variant not provided [RCV000079452] Chr19:36055127 [GRCh38]
Chr19:36546029 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2227C>T (p.His743Tyr) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000282054]|not provided [RCV000079453] Chr19:36092705 [GRCh38]
Chr19:36583607 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3929A>T (p.Gln1310Leu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576369]|not provided [RCV000710286]|not specified [RCV000079454] Chr19:36103757 [GRCh38]
Chr19:36594659 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.3946C>G (p.Gln1316Glu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000311851]|not provided [RCV000421199]|not specified [RCV000079455] Chr19:36103774 [GRCh38]
Chr19:36594676 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.700-18C>T single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000604973]|not specified [RCV000147978] Chr19:36067810 [GRCh38]
Chr19:36558712 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.1642+8C>T single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000270317]|not provided [RCV000993552]|not specified [RCV000147919] Chr19:36084752 [GRCh38]
Chr19:36575654 [GRCh37]
Chr19:19q13.12
benign|uncertain significance
NM_001083961.2(WDR62):c.2281C>T (p.His761Tyr) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000372973]|not provided [RCV000957950]|not specified [RCV000147932] Chr19:36092759 [GRCh38]
Chr19:36583661 [GRCh37]
Chr19:19q13.12
benign|uncertain significance
NM_001083961.2(WDR62):c.186C>T (p.Leu62=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576337]|not specified [RCV000147927] Chr19:36058788 [GRCh38]
Chr19:36549690 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.2991C>T (p.Ala997=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000606501]|not provided [RCV000993553]|not specified [RCV000147947] Chr19:36101683 [GRCh38]
Chr19:36592585 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.2016C>T (p.Asp672=) single nucleotide variant not provided [RCV000959548]|not specified [RCV000175022] Chr19:36090502 [GRCh38]
Chr19:36581404 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.1641G>T (p.Thr547=) single nucleotide variant not provided [RCV000514453]|not specified [RCV000174279] Chr19:36084743 [GRCh38]
Chr19:36575645 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.2112G>C (p.Ser704=) single nucleotide variant not provided [RCV000959549]|not specified [RCV000175152] Chr19:36091277 [GRCh38]
Chr19:36582179 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.2666T>C (p.Met889Thr) single nucleotide variant not provided [RCV000514943]|not specified [RCV000176278] Chr19:36099544 [GRCh38]
Chr19:36590446 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.3271_3273del (p.His1091del) deletion not specified [RCV000176723] Chr19:36102785..36102787 [GRCh38]
Chr19:36593687..36593689 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.28G>T (p.Ala10Ser) single nucleotide variant not provided [RCV000173203] Chr19:36054999 [GRCh38]
Chr19:36545901 [GRCh37]
Chr19:19q13.12
uncertain significance
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31
pathogenic
NM_001083961.2(WDR62):c.1873G>A (p.Val625Ile) single nucleotide variant not provided [RCV000174857] Chr19:36089221 [GRCh38]
Chr19:36580123 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1769-7C>T single nucleotide variant not provided [RCV000174702] Chr19:36089031 [GRCh38]
Chr19:36579933 [GRCh37]
Chr19:19q13.12
conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.*5G>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147908]|not specified [RCV000154148] Chr19:36105033 [GRCh38]
Chr19:36595935 [GRCh37]
Chr19:19q13.12
benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.1043+3A>G single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147909]|not provided [RCV000344609] Chr19:36071719 [GRCh38]
Chr19:36562621 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1225A>G (p.Asn409Asp) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000755657]|not provided [RCV000439209]|not specified [RCV000147910] Chr19:36073523 [GRCh38]
Chr19:36564425 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.1233+13C>T single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000336060]|not specified [RCV000147911] Chr19:36073544 [GRCh38]
Chr19:36564446 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.1312C>T (p.Arg438Cys) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147912] Chr19:36081511 [GRCh38]
Chr19:36572413 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.1315T>G (p.Phe439Val) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126009]|not provided [RCV000959547]|not specified [RCV000147913] Chr19:36081514 [GRCh38]
Chr19:36572416 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.1470C>T (p.Asp490=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576725]|not specified [RCV000147914] Chr19:36083161 [GRCh38]
Chr19:36574063 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.1480G>A (p.Gly494Arg) single nucleotide variant Inborn genetic diseases [RCV000622916]|Primary autosomal recessive microcephaly 2 [RCV000147915] Chr19:36083171 [GRCh38]
Chr19:36574073 [GRCh37]
Chr19:19q13.12
likely pathogenic|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.1486C>T (p.Arg496Trp) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147916] Chr19:36083177 [GRCh38]
Chr19:36574079 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1534C>G (p.Arg512Gly) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147917] Chr19:36083225 [GRCh38]
Chr19:36574127 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1641G>A (p.Thr547=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576339]|not specified [RCV000147918] Chr19:36084743 [GRCh38]
Chr19:36575645 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.1643-10C>T single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576467]|not specified [RCV000147920] Chr19:36086677 [GRCh38]
Chr19:36577579 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.1643-39G>A single nucleotide variant not provided [RCV000833253]|not specified [RCV000147921] Chr19:36086648 [GRCh38]
Chr19:36577550 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.1681A>T (p.Ile561Phe) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147922] Chr19:36086725 [GRCh38]
Chr19:36577627 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1750A>C (p.Thr584Pro) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147923] Chr19:36086794 [GRCh38]
Chr19:36577696 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1768+28G>A single nucleotide variant not provided [RCV000829620]|not specified [RCV000147924] Chr19:36086840 [GRCh38]
Chr19:36577742 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.180G>A (p.Val60=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576720]|not specified [RCV000147925] Chr19:36058782 [GRCh38]
Chr19:36549684 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.186C>G (p.Leu62=) single nucleotide variant not specified [RCV000147926] Chr19:36058788 [GRCh38]
Chr19:36549690 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2084_2090dup (p.Ser698fs) duplication Primary autosomal recessive microcephaly 2 [RCV000147928] Chr19:36091248..36091249 [GRCh38]
Chr19:36582150..36582151 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.2147-34G>A single nucleotide variant not provided [RCV000829621]|not specified [RCV000147929] Chr19:36091368 [GRCh38]
Chr19:36582270 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.2211-4G>A single nucleotide variant Intellectual disability [RCV001252633]|Primary autosomal recessive microcephaly 2 [RCV000385338]|not provided [RCV000725516]|not specified [RCV000147930] Chr19:36092685 [GRCh38]
Chr19:36583587 [GRCh37]
Chr19:19q13.12
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.2271G>A (p.Leu757=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576533]|not specified [RCV000147931] Chr19:36092749 [GRCh38]
Chr19:36583651 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.2312A>G (p.Lys771Arg) single nucleotide variant not provided [RCV000714192]|not specified [RCV000147933] Chr19:36092790 [GRCh38]
Chr19:36583692 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2334-29C>T single nucleotide variant not provided [RCV000833281]|not specified [RCV000147934] Chr19:36094002 [GRCh38]
Chr19:36584904 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.2334-6C>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125144]|not provided [RCV000710283]|not specified [RCV000147935] Chr19:36094025 [GRCh38]
Chr19:36584927 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.2490C>T (p.Asn830=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147936] Chr19:36097049 [GRCh38]
Chr19:36587951 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2529C>T (p.Asp843=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126112]|not provided [RCV000900040]|not specified [RCV000310697] Chr19:36099407 [GRCh38]
Chr19:36590309 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.2549T>C (p.Leu850Ser) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576671]|not provided [RCV000710284]|not specified [RCV000147938] Chr19:36099427 [GRCh38]
Chr19:36590329 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.2566C>T (p.Arg856Cys) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147939] Chr19:36099444 [GRCh38]
Chr19:36590346 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2584G>T (p.Gly862Cys) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147940] Chr19:36099462 [GRCh38]
Chr19:36590364 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2655C>G (p.Tyr885Ter) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147941] Chr19:36099533 [GRCh38]
Chr19:36590435 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.2782C>T (p.Leu928=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147942] Chr19:36100790 [GRCh38]
Chr19:36591692 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2896G>A (p.Gly966Arg) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147943] Chr19:36101242 [GRCh38]
Chr19:36592144 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2945G>A (p.Ser982Asn) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147944] Chr19:36101291 [GRCh38]
Chr19:36592193 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2975C>T (p.Ser992Leu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128200]|not provided [RCV000947937]|not specified [RCV000147945] Chr19:36101667 [GRCh38]
Chr19:36592569 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.2982G>A (p.Glu994=) single nucleotide variant not specified [RCV000147946] Chr19:36101674 [GRCh38]
Chr19:36592576 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3033G>A (p.Pro1011=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128202]|not provided [RCV000885269]|not specified [RCV000147948] Chr19:36101725 [GRCh38]
Chr19:36592627 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.3066G>A (p.Ser1022=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147949] Chr19:36101758 [GRCh38]
Chr19:36592660 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.32G>C (p.Arg11Pro) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147950] Chr19:36055003 [GRCh38]
Chr19:36545905 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3303G>A (p.Thr1101=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000330613]|not provided [RCV000723854]|not specified [RCV000147951] Chr19:36102819 [GRCh38]
Chr19:36593721 [GRCh37]
Chr19:19q13.12
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.332+1G>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147952] Chr19:36060031 [GRCh38]
Chr19:36550933 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.3335+3A>G single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147953] Chr19:36102854 [GRCh38]
Chr19:36593756 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.3336-5C>G single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147954] Chr19:36102943 [GRCh38]
Chr19:36593845 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3401T>G (p.Met1134Arg) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576353]|not specified [RCV000147955] Chr19:36103013 [GRCh38]
Chr19:36593915 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.3406C>G (p.Arg1136Gly) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147956] Chr19:36103018 [GRCh38]
Chr19:36593920 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3468C>T (p.Leu1156=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576554]|not specified [RCV000147957] Chr19:36103161 [GRCh38]
Chr19:36594063 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.3514+44G>A single nucleotide variant not provided [RCV000829623]|not specified [RCV000147958] Chr19:36103251 [GRCh38]
Chr19:36594153 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.3515-7G>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147959] Chr19:36103336 [GRCh38]
Chr19:36594238 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3559G>A (p.Val1187Met) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147960] Chr19:36103387 [GRCh38]
Chr19:36594289 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3573C>T (p.Asp1191=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147961] Chr19:36103401 [GRCh38]
Chr19:36594303 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.359C>A (p.Ser120Tyr) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147962] Chr19:36065984 [GRCh38]
Chr19:36556886 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.3611G>T (p.Gly1204Val) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147963] Chr19:36103439 [GRCh38]
Chr19:36594341 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3639C>T (p.Ser1213=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576754]|not specified [RCV000147964] Chr19:36103467 [GRCh38]
Chr19:36594369 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.3674G>A (p.Arg1225His) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000348138]|not provided [RCV000710285]|not specified [RCV000147965] Chr19:36103502 [GRCh38]
Chr19:36594404 [GRCh37]
Chr19:19q13.12
benign|uncertain significance
NM_001083961.2(WDR62):c.3698C>G (p.Ser1233Cys) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147966] Chr19:36103526 [GRCh38]
Chr19:36594428 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3948G>A (p.Gln1316=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147968] Chr19:36103776 [GRCh38]
Chr19:36594678 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4123G>A (p.Gly1375Ser) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576586]|not specified [RCV000147969] Chr19:36103951 [GRCh38]
Chr19:36594853 [GRCh37]
Chr19:19q13.12
benign|uncertain significance
NM_001083961.2(WDR62):c.4153+37C>G single nucleotide variant not specified [RCV000147970] Chr19:36104018 [GRCh38]
Chr19:36594920 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.4159C>A (p.Leu1387Ile) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000301172]|not provided [RCV000724024]|not specified [RCV000177523] Chr19:36104523 [GRCh38]
Chr19:36595425 [GRCh37]
Chr19:19q13.12
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.4170A>C (p.Leu1390Phe) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000576791]|not provided [RCV000710287]|not specified [RCV000147972] Chr19:36104534 [GRCh38]
Chr19:36595436 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.4312-5T>G single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000361714]|not provided [RCV000585061]|not specified [RCV000147973] Chr19:36104763 [GRCh38]
Chr19:36595665 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.4381T>G (p.Trp1461Gly) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147974] Chr19:36104837 [GRCh38]
Chr19:36595739 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.561+44C>G single nucleotide variant not specified [RCV000147975] Chr19:36066471 [GRCh38]
Chr19:36557373 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.562-13C>T single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000328288]|not specified [RCV000147976] Chr19:36067293 [GRCh38]
Chr19:36558195 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.589G>A (p.Val197Ile) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147977] Chr19:36067333 [GRCh38]
Chr19:36558235 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.82C>G (p.Arg28Gly) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147979] Chr19:36055053 [GRCh38]
Chr19:36545955 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.866A>G (p.Lys289Arg) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000294039]|not provided [RCV000432829]|not specified [RCV000147980] Chr19:36067994 [GRCh38]
Chr19:36558896 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.964G>C (p.Ala322Pro) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000147981] Chr19:36071637 [GRCh38]
Chr19:36562539 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2040T>C (p.His680=) single nucleotide variant not provided [RCV000175151] Chr19:36091205 [GRCh38]
Chr19:36582107 [GRCh37]
Chr19:19q13.12
conflicting interpretations of pathogenicity|uncertain significance
GRCh38/hg38 19q12-13.13(chr19:29661858-38114723)x1 copy number loss See cases [RCV000135879] Chr19:29661858..38114723 [GRCh38]
Chr19:30152765..38605363 [GRCh37]
Chr19:34844605..43297203 [NCBI36]
Chr19:19q12-13.13
pathogenic
GRCh38/hg38 19q12-13.13(chr19:29671324-37902990)x1 copy number loss See cases [RCV000136794] Chr19:29671324..37902990 [GRCh38]
Chr19:30162231..38393630 [GRCh37]
Chr19:34854071..43085470 [NCBI36]
Chr19:19q12-13.13
pathogenic
NM_001083961.2(WDR62):c.109G>C (p.Ala37Pro) single nucleotide variant not specified [RCV000202678] Chr19:36055080 [GRCh38]
Chr19:36545982 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.1228G>T (p.Val410Leu) single nucleotide variant not provided [RCV000723848]|not specified [RCV000154145] Chr19:36073526 [GRCh38]
Chr19:36564428 [GRCh37]
Chr19:19q13.12
conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.1233+7C>G single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126005]|not provided [RCV000154146] Chr19:36073538 [GRCh38]
Chr19:36564440 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.189G>T (p.Glu63Asp) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128005]|not provided [RCV000175656] Chr19:36058791 [GRCh38]
Chr19:36549693 [GRCh37]
Chr19:19q13.12
conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.3612C>T (p.Gly1204=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000376054]|not provided [RCV000725011]|not specified [RCV000192844] Chr19:36103440 [GRCh38]
Chr19:36594342 [GRCh37]
Chr19:19q13.12
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.413G>A (p.Arg138His) single nucleotide variant not specified [RCV000192911] Chr19:36066279 [GRCh38]
Chr19:36557181 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1359C>T (p.Asn453=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000404359]|not provided [RCV000962681]|not specified [RCV000193171] Chr19:36081558 [GRCh38]
Chr19:36572460 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.656G>A (p.Arg219His) single nucleotide variant not specified [RCV000193274] Chr19:36067400 [GRCh38]
Chr19:36558302 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1667G>T (p.Ser556Ile) single nucleotide variant not specified [RCV000193620] Chr19:36086711 [GRCh38]
Chr19:36577613 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4187G>A (p.Arg1396His) single nucleotide variant Intellectual disability [RCV001252634]|Primary autosomal recessive microcephaly 2 [RCV001128275]|not specified [RCV000193946] Chr19:36104551 [GRCh38]
Chr19:36595453 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1509C>T (p.Asp503=) single nucleotide variant not provided [RCV000880350]|not specified [RCV000194207] Chr19:36083200 [GRCh38]
Chr19:36574102 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.4564G>A (p.Gly1522Arg) single nucleotide variant not specified [RCV000195227] Chr19:36105020 [GRCh38]
Chr19:36595922 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3232G>A (p.Ala1078Thr) single nucleotide variant not provided [RCV000176724] Chr19:36102748 [GRCh38]
Chr19:36593650 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1233+15dup duplication Primary Microcephaly 2 With or Without Cortical Malformations [RCV000392212]|not specified [RCV000180555] Chr19:36073536..36073537 [GRCh38]
Chr19:36564438..36564439 [GRCh37]
Chr19:19q13.12
benign|uncertain significance
NM_001083961.2(WDR62):c.1170C>T (p.Asp390=) single nucleotide variant not provided [RCV000180556] Chr19:36073468 [GRCh38]
Chr19:36564370 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2887G>A (p.Val963Met) single nucleotide variant not provided [RCV000176463] Chr19:36101233 [GRCh38]
Chr19:36592135 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3786C>T (p.Gly1262=) single nucleotide variant not provided [RCV000905790]|not specified [RCV000177447] Chr19:36103614 [GRCh38]
Chr19:36594516 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.3812C>T (p.Ala1271Val) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000351552]|not provided [RCV000714196]|not specified [RCV000193857] Chr19:36103640 [GRCh38]
Chr19:36594542 [GRCh37]
Chr19:19q13.12
benign|likely benign|uncertain significance
NM_001083961.2(WDR62):c.2976G>A (p.Ser992=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128201]|not provided [RCV000724032]|not specified [RCV000176536] Chr19:36101668 [GRCh38]
Chr19:36592570 [GRCh37]
Chr19:19q13.12
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.4403C>T (p.Ala1468Val) single nucleotide variant not provided [RCV000177633] Chr19:36104859 [GRCh38]
Chr19:36595761 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1233+15del deletion Primary Microcephaly 2 With or Without Cortical Malformations [RCV000299793]|not specified [RCV000192527] Chr19:36073537 [GRCh38]
Chr19:36564439 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.269+12del deletion Primary Microcephaly 2 With or Without Cortical Malformations [RCV000273209]|not specified [RCV000193786] Chr19:36058882 [GRCh38]
Chr19:36549784 [GRCh37]
Chr19:19q13.12
benign|uncertain significance
NM_001083961.2(WDR62):c.2057C>T (p.Thr686Ile) single nucleotide variant not specified [RCV000194657] Chr19:36091222 [GRCh38]
Chr19:36582124 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3348del (p.Phe1117fs) deletion Primary autosomal recessive microcephaly 2 [RCV000194814] Chr19:36102959 [GRCh38]
Chr19:36593861 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.3818C>T (p.Thr1273Ile) single nucleotide variant not specified [RCV000194894] Chr19:36103646 [GRCh38]
Chr19:36594548 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.1(WDR62):c.2030T>C single nucleotide variant Abnormality of neuronal migration [RCV000201429] Chr19:36090516 [GRCh38]
Chr19:36581418 [GRCh37]
Chr19:19q13.12
pathogenic|uncertain significance
NM_001083961.2(WDR62):c.3231C>T (p.Pro1077=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000369864]|not provided [RCV000973795]|not specified [RCV000329087] Chr19:36102747 [GRCh38]
Chr19:36593649 [GRCh37]
Chr19:19q13.12
benign|uncertain significance
NM_001083961.2(WDR62):c.1696G>A (p.Val566Met) single nucleotide variant not provided [RCV000518930] Chr19:36086740 [GRCh38]
Chr19:36577642 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1941C>A (p.Cys647Ter) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000763424]|not provided [RCV000330039] Chr19:36089289 [GRCh38]
Chr19:36580191 [GRCh37]
Chr19:19q13.12
pathogenic
GRCh37/hg19 19q13.12-13.13(chr19:36475577-38399402)x3 copy number gain See cases [RCV000240597] Chr19:36475577..38399402 [GRCh37]
Chr19:19q13.12-13.13
uncertain significance
NM_001083961.2(WDR62):c.2605G>A (p.Gly869Ser) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000284673] Chr19:36099483 [GRCh38]
Chr19:36590385 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3536C>T (p.Ala1179Val) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000287371] Chr19:36103364 [GRCh38]
Chr19:36594266 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3810C>T (p.Thr1270=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000289537]|not provided [RCV000841474] Chr19:36103638 [GRCh38]
Chr19:36594540 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.4339G>A (p.Gly1447Arg) single nucleotide variant Microcephaly, Cortical Malformations, and Intellectual Disability [RCV000325259]|Primary Microcephaly, Recessive [RCV000383411]|Primary autosomal recessive microcephaly 2 [RCV000272612] Chr19:36104795 [GRCh38]
Chr19:36595697 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.*45G>C single nucleotide variant Microcephaly, Cortical Malformations, and Intellectual Disability [RCV000337117]|Primary Microcephaly, Recessive [RCV000293868]|Primary autosomal recessive microcephaly 2 [RCV000385832] Chr19:36105073 [GRCh38]
Chr19:36595975 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4546G>A (p.Val1516Met) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000294985] Chr19:36105002 [GRCh38]
Chr19:36595904 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3724G>A (p.Val1242Met) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000392015] Chr19:36103552 [GRCh38]
Chr19:36594454 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3161C>G (p.Pro1054Arg) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000309409] Chr19:36102092 [GRCh38]
Chr19:36592994 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1521G>A (p.Leu507=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001007662] Chr19:36083212 [GRCh38]
Chr19:36574114 [GRCh37]
Chr19:19q13.12
pathogenic|uncertain significance
NM_001083961.2(WDR62):c.4481A>G (p.Tyr1494Cys) single nucleotide variant not provided [RCV000306345] Chr19:36104937 [GRCh38]
Chr19:36595839 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4296C>T (p.Leu1432=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000323392]|not specified [RCV000437050] Chr19:36104660 [GRCh38]
Chr19:36595562 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.3302C>T (p.Thr1101Met) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000275471]|not provided [RCV000728987] Chr19:36102818 [GRCh38]
Chr19:36593720 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1977C>T (p.Asn659=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000276246]|not provided [RCV000731427] Chr19:36090463 [GRCh38]
Chr19:36581365 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4266C>T (p.His1422=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000261229] Chr19:36104630 [GRCh38]
Chr19:36595532 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1064C>T (p.Ala355Val) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000349086] Chr19:36073362 [GRCh38]
Chr19:36564264 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2467+2T>G single nucleotide variant not provided [RCV000311645] Chr19:36094166 [GRCh38]
Chr19:36585068 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.4549C>T (p.Arg1517Trp) single nucleotide variant not provided [RCV000382032] Chr19:36105005 [GRCh38]
Chr19:36595907 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4329G>A (p.Gln1443=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000321785]|not provided [RCV000658827] Chr19:36104785 [GRCh38]
Chr19:36595687 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3360G>A (p.Arg1120=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000262539] Chr19:36102972 [GRCh38]
Chr19:36593874 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3537G>A (p.Ala1179=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000323689] Chr19:36103365 [GRCh38]
Chr19:36594267 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1642+9G>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000325362]|not provided [RCV000931270] Chr19:36084753 [GRCh38]
Chr19:36575655 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.2766C>T (p.Arg922=) single nucleotide variant not provided [RCV000725405]|not specified [RCV000349577] Chr19:36100774 [GRCh38]
Chr19:36591676 [GRCh37]
Chr19:19q13.12
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.*45G>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000352224] Chr19:36105073 [GRCh38]
Chr19:36595975 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.820T>G (p.Tyr274Asp) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000352612]|not provided [RCV000591660] Chr19:36067948 [GRCh38]
Chr19:36558850 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.253G>A (p.Val85Met) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000765442]|not provided [RCV000996849]|not specified [RCV000504021] Chr19:36058855 [GRCh38]
Chr19:36549757 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4144C>T (p.Pro1382Ser) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000402904] Chr19:36103972 [GRCh38]
Chr19:36594874 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.791G>A (p.Arg264Gln) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000288306] Chr19:36067919 [GRCh38]
Chr19:36558821 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2007C>T (p.Ser669=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000330751] Chr19:36090493 [GRCh38]
Chr19:36581395 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1489G>A (p.Val497Ile) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000264352] Chr19:36083180 [GRCh38]
Chr19:36574082 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4464G>A (p.Pro1488=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000382322] Chr19:36104920 [GRCh38]
Chr19:36595822 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2972A>T (p.Asp991Val) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000390654]|not specified [RCV000504304] Chr19:36101664 [GRCh38]
Chr19:36592566 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1479C>T (p.Ala493=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000359082]|not provided [RCV000892360] Chr19:36083170 [GRCh38]
Chr19:36574072 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.2610A>G (p.Gln870=) single nucleotide variant not provided [RCV000259708] Chr19:36099488 [GRCh38]
Chr19:36590390 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4338C>T (p.Thr1446=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122565]|not provided [RCV000887271]|not specified [RCV000293512] Chr19:36104794 [GRCh38]
Chr19:36595696 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.2580C>T (p.Pro860=) single nucleotide variant not provided [RCV000397337] Chr19:36099458 [GRCh38]
Chr19:36590360 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2521-13G>C single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000342707] Chr19:36099386 [GRCh38]
Chr19:36590288 [GRCh37]
Chr19:19q13.12
benign|uncertain significance
NM_001083961.2(WDR62):c.37G>C (p.Asp13His) single nucleotide variant not provided [RCV000400632] Chr19:36055008 [GRCh38]
Chr19:36545910 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3220+4G>C single nucleotide variant Microcephaly, Cortical Malformations, and Intellectual Disability [RCV000405859]|Primary Microcephaly, Recessive [RCV000363841]|Primary autosomal recessive microcephaly 2 [RCV000315202] Chr19:36102155 [GRCh38]
Chr19:36593057 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4312T>A (p.Leu1438Met) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000264715]|not specified [RCV000502642] Chr19:36104768 [GRCh38]
Chr19:36595670 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.477G>A (p.Ala159=) single nucleotide variant not provided [RCV000725073]|not specified [RCV000366094] Chr19:36066343 [GRCh38]
Chr19:36557245 [GRCh37]
Chr19:19q13.12
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.82C>T (p.Arg28Trp) single nucleotide variant not provided [RCV000403150] Chr19:36055053 [GRCh38]
Chr19:36545955 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.10G>C (p.Val4Leu) single nucleotide variant Primary Microcephaly 2 With or Without Cortical Malformations [RCV000362050]|not provided [RCV000487630] Chr19:36054981 [GRCh38]
Chr19:36545883 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1342T>A (p.Ser448Thr) single nucleotide variant not provided [RCV000725924]|not specified [RCV000266233] Chr19:36081541 [GRCh38]
Chr19:36572443 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3162G>A (p.Pro1054=) single nucleotide variant not provided [RCV000335791] Chr19:36102093 [GRCh38]
Chr19:36592995 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.303C>A (p.Asn101Lys) single nucleotide variant not provided [RCV000489187] Chr19:36060001 [GRCh38]
Chr19:36550903 [GRCh37]
Chr19:19q13.12
conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.3733C>A (p.Leu1245Met) single nucleotide variant not provided [RCV000489248] Chr19:36103561 [GRCh38]
Chr19:36594463 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.525C>T (p.Tyr175=) single nucleotide variant not provided [RCV000597667] Chr19:36066391 [GRCh38]
Chr19:36557293 [GRCh37]
Chr19:19q13.12
conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.2263del (p.His755fs) deletion not provided [RCV000487677] Chr19:36092741 [GRCh38]
Chr19:36583643 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.2269C>G (p.Leu757Val) single nucleotide variant not provided [RCV000487961] Chr19:36092747 [GRCh38]
Chr19:36583649 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.761_763TCT[1] (p.Phe255del) microsatellite not provided [RCV000488031] Chr19:36067889..36067891 [GRCh38]
Chr19:36558791..36558793 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3309C>A (p.Phe1103Leu) single nucleotide variant not provided [RCV000488353] Chr19:36102825 [GRCh38]
Chr19:36593727 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1640C>T (p.Thr547Met) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000627094]|not provided [RCV000488384] Chr19:36084742 [GRCh38]
Chr19:36575644 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.699+11G>C single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000382805] Chr19:36067454 [GRCh38]
Chr19:36558356 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.1(WDR62):c.3304C>T single nucleotide variant not provided [RCV000521576] Chr19:36102820 [GRCh38]
Chr19:36593722 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.821A>G (p.Tyr274Cys) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000388425] Chr19:36067949 [GRCh38]
Chr19:36558851 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2237C>T (p.Pro746Leu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125142]|not provided [RCV000598120] Chr19:36092715 [GRCh38]
Chr19:36583617 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1575C>T (p.Asp525=) single nucleotide variant not provided [RCV000941736]|not specified [RCV000604813] Chr19:36084677 [GRCh38]
Chr19:36575579 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2787C>T (p.Pro929=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000339653] Chr19:36100795 [GRCh38]
Chr19:36591697 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3356C>T (p.Pro1119Leu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000357272] Chr19:36102968 [GRCh38]
Chr19:36593870 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4122C>T (p.Gly1374=) single nucleotide variant not provided [RCV000592540] Chr19:36103950 [GRCh38]
Chr19:36594852 [GRCh37]
Chr19:19q13.12
conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.1238A>T (p.Tyr413Phe) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126008]|not provided [RCV000522837] Chr19:36081437 [GRCh38]
Chr19:36572339 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.203T>C (p.Ile68Thr) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000765441]|not provided [RCV000596646]|not specified [RCV001174862] Chr19:36058805 [GRCh38]
Chr19:36549707 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4226dup (p.Ser1410fs) duplication not provided [RCV000598976] Chr19:36104585..36104586 [GRCh38]
Chr19:36595487..36595488 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.700G>T (p.Val234Leu) single nucleotide variant not provided [RCV000585535] Chr19:36067828 [GRCh38]
Chr19:36558730 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1927G>A (p.Val643Met) single nucleotide variant not provided [RCV000597588] Chr19:36089275 [GRCh38]
Chr19:36580177 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1371+6T>G single nucleotide variant not provided [RCV000597895] Chr19:36081576 [GRCh38]
Chr19:36572478 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2527G>T (p.Asp843Tyr) single nucleotide variant not provided [RCV000598239] Chr19:36099405 [GRCh38]
Chr19:36590307 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3596C>G (p.Ser1199Cys) single nucleotide variant not provided [RCV000731091] Chr19:36103424 [GRCh38]
Chr19:36594326 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1677_1680dup (p.Ile561fs) duplication not provided [RCV000733781] Chr19:36086719..36086720 [GRCh38]
Chr19:36577621..36577622 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.4441G>A (p.Ala1481Thr) single nucleotide variant not provided [RCV000595507] Chr19:36104897 [GRCh38]
Chr19:36595799 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3221A>G (p.Glu1074Gly) single nucleotide variant not provided [RCV000728598] Chr19:36102737 [GRCh38]
Chr19:36593639 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3058G>A (p.Ala1020Thr) single nucleotide variant not provided [RCV000730480] Chr19:36101750 [GRCh38]
Chr19:36592652 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3763G>A (p.Val1255Ile) single nucleotide variant not provided [RCV000416274]|not specified [RCV000606043] Chr19:36103591 [GRCh38]
Chr19:36594493 [GRCh37]
Chr19:19q13.12
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001083961.2(WDR62):c.3641C>T (p.Thr1214Ile) single nucleotide variant not provided [RCV000733372] Chr19:36103469 [GRCh38]
Chr19:36594371 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1987_1989AAG[1] (p.Lys664del) microsatellite Intellectual disability [RCV001255364]|not provided [RCV000734747] Chr19:36090471..36090473 [GRCh38]
Chr19:36581373..36581375 [GRCh37]
Chr19:19q13.12
likely pathogenic|uncertain significance
NM_001083961.2(WDR62):c.2318G>A (p.Arg773Gln) single nucleotide variant not provided [RCV000729673] Chr19:36092796 [GRCh38]
Chr19:36583698 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3937G>A (p.Val1313Met) single nucleotide variant not specified [RCV000413045] Chr19:36103765 [GRCh38]
Chr19:36594667 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.778T>C (p.Cys260Arg) single nucleotide variant not provided [RCV000413566] Chr19:36067906 [GRCh38]
Chr19:36558808 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.1959-10A>C single nucleotide variant not provided [RCV000595004] Chr19:36090435 [GRCh38]
Chr19:36581337 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.*84T>A single nucleotide variant not specified [RCV000734282] Chr19:36105112 [GRCh38]
Chr19:36596014 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.699+16T>C single nucleotide variant not specified [RCV000431185] Chr19:36067459 [GRCh38]
Chr19:36558361 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2739+16G>A single nucleotide variant not specified [RCV000434847] Chr19:36099633 [GRCh38]
Chr19:36590535 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3540C>T (p.Ser1180=) single nucleotide variant not provided [RCV000889611]|not specified [RCV000418410] Chr19:36103368 [GRCh38]
Chr19:36594270 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3480G>A (p.Lys1160=) single nucleotide variant not specified [RCV000438923] Chr19:36103173 [GRCh38]
Chr19:36594075 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1842G>A (p.Ser614=) single nucleotide variant not specified [RCV000428706] Chr19:36089190 [GRCh38]
Chr19:36580092 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.700-15C>A single nucleotide variant not specified [RCV000435405] Chr19:36067813 [GRCh38]
Chr19:36558715 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1768+18C>T single nucleotide variant not specified [RCV000421800] Chr19:36086830 [GRCh38]
Chr19:36577732 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1959-20A>G single nucleotide variant not specified [RCV000425295] Chr19:36090425 [GRCh38]
Chr19:36581327 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.269+19C>T single nucleotide variant not specified [RCV000422115] Chr19:36058890 [GRCh38]
Chr19:36549792 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.570C>T (p.Ile190=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122248]|not specified [RCV000439840] Chr19:36067314 [GRCh38]
Chr19:36558216 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.1752C>T (p.Thr584=) single nucleotide variant not specified [RCV000419897] Chr19:36086796 [GRCh38]
Chr19:36577698 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.390+7C>T single nucleotide variant not specified [RCV000420020] Chr19:36066022 [GRCh38]
Chr19:36556924 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2739+19G>A single nucleotide variant not specified [RCV000429675] Chr19:36099636 [GRCh38]
Chr19:36590538 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3702C>T (p.Leu1234=) single nucleotide variant not specified [RCV000440325] Chr19:36103530 [GRCh38]
Chr19:36594432 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.4105C>A (p.Arg1369=) single nucleotide variant not specified [RCV000437349] Chr19:36103933 [GRCh38]
Chr19:36594835 [GRCh37]
Chr19:19q13.12
likely benign
GRCh37/hg19 19q13.12(chr19:36551768-36582304)x1 copy number loss See cases [RCV000448985] Chr19:36551768..36582304 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4186C>T (p.Arg1396Cys) single nucleotide variant not provided [RCV000483776] Chr19:36104550 [GRCh38]
Chr19:36595452 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4006G>A (p.Ala1336Thr) single nucleotide variant not provided [RCV000481526] Chr19:36103834 [GRCh38]
Chr19:36594736 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4264_4265delinsGTGGTCTGAG (p.His1422delinsValValTer) indel not provided [RCV000480506] Chr19:36104628..36104629 [GRCh38]
Chr19:36595530..36595531 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.540G>A (p.Val180=) single nucleotide variant not specified [RCV000501066] Chr19:36066406 [GRCh38]
Chr19:36557308 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.4005C>A (p.Ser1335Arg) single nucleotide variant not specified [RCV000501048] Chr19:36103833 [GRCh38]
Chr19:36594735 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3514+1G>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000501183]|not provided [RCV000727460] Chr19:36103208 [GRCh38]
Chr19:36594110 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.4501C>T (p.Leu1501=) single nucleotide variant not specified [RCV000503853] Chr19:36104957 [GRCh38]
Chr19:36595859 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3012_3034dup (p.Pro1012fs) duplication Primary autosomal recessive microcephaly 2 [RCV000504101] Chr19:36101700..36101701 [GRCh38]
Chr19:36592602..36592603 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.1095G>T (p.Leu365=) single nucleotide variant not specified [RCV000499455] Chr19:36073393 [GRCh38]
Chr19:36564295 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3589C>A (p.Pro1197Thr) single nucleotide variant not specified [RCV000501966] Chr19:36103417 [GRCh38]
Chr19:36594319 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1434C>G (p.Phe478Leu) single nucleotide variant not specified [RCV000504435] Chr19:36083125 [GRCh38]
Chr19:36574027 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3247G>A (p.Val1083Met) single nucleotide variant not specified [RCV000499854] Chr19:36102763 [GRCh38]
Chr19:36593665 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1836+34G>T single nucleotide variant not specified [RCV000499882] Chr19:36089139 [GRCh38]
Chr19:36580041 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2729T>A (p.Leu910Gln) single nucleotide variant not specified [RCV000502215] Chr19:36099607 [GRCh38]
Chr19:36590509 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4527G>A (p.Ser1509=) single nucleotide variant not specified [RCV000502266] Chr19:36104983 [GRCh38]
Chr19:36595885 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3954C>T (p.Gly1318=) single nucleotide variant not specified [RCV000500166] Chr19:36103782 [GRCh38]
Chr19:36594684 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.4153G>A (p.Gly1385Ser) single nucleotide variant not specified [RCV000500382] Chr19:36103981 [GRCh38]
Chr19:36594883 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2584G>A (p.Gly862Ser) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000500750] Chr19:36099462 [GRCh38]
Chr19:36590364 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.831C>T (p.Leu277=) single nucleotide variant not provided [RCV000714197]|not specified [RCV000503167] Chr19:36067959 [GRCh38]
Chr19:36558861 [GRCh37]
Chr19:19q13.12
likely benign
GRCh37/hg19 19q13.12(chr19:36147111-37249653)x1 copy number loss See cases [RCV000511504] Chr19:36147111..37249653 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.952C>T (p.Arg318Cys) single nucleotide variant not provided [RCV000493749] Chr19:36071625 [GRCh38]
Chr19:36562527 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.16T>G (p.Ser6Ala) single nucleotide variant not provided [RCV000714190] Chr19:36054987 [GRCh38]
Chr19:36545889 [GRCh37]
Chr19:19q13.12
uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic|uncertain significance
NM_001083961.2(WDR62):c.693G>A (p.Glu231=) single nucleotide variant not specified [RCV000604878] Chr19:36067437 [GRCh38]
Chr19:36558339 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3748C>G (p.Arg1250Gly) single nucleotide variant not provided [RCV000594986] Chr19:36103576 [GRCh38]
Chr19:36594478 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.231C>A (p.Thr77=) single nucleotide variant not specified [RCV000606471] Chr19:36058833 [GRCh38]
Chr19:36549735 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.744C>T (p.Gly248=) single nucleotide variant not provided [RCV000906193]|not specified [RCV000601247] Chr19:36067872 [GRCh38]
Chr19:36558774 [GRCh37]
Chr19:19q13.12
benign|likely benign
NM_001083961.2(WDR62):c.2972-15G>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000601614] Chr19:36101649 [GRCh38]
Chr19:36592551 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3621G>A (p.Gln1207=) single nucleotide variant not specified [RCV000602374] Chr19:36103449 [GRCh38]
Chr19:36594351 [GRCh37]
Chr19:19q13.12
likely benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
NM_001083961.2(WDR62):c.-35A>G single nucleotide variant not specified [RCV000607928] Chr19:36054937 [GRCh38]
Chr19:36545839 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2343G>A (p.Thr781=) single nucleotide variant not provided [RCV000916424]|not specified [RCV000609459] Chr19:36094040 [GRCh38]
Chr19:36584942 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3087C>T (p.Cys1029=) single nucleotide variant not provided [RCV000714194]|not specified [RCV000605559] Chr19:36102018 [GRCh38]
Chr19:36592920 [GRCh37]
Chr19:19q13.12
likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.1764C>T (p.Phe588=) single nucleotide variant not specified [RCV000612604] Chr19:36086808 [GRCh38]
Chr19:36577710 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1551-16G>A single nucleotide variant not specified [RCV000615856] Chr19:36084637 [GRCh38]
Chr19:36575539 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3440A>G (p.Tyr1147Cys) single nucleotide variant not provided [RCV000595542] Chr19:36103052 [GRCh38]
Chr19:36593954 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4311+16G>T single nucleotide variant not specified [RCV000614127] Chr19:36104691 [GRCh38]
Chr19:36595593 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2381C>G (p.Pro794Arg) single nucleotide variant not provided [RCV000595648] Chr19:36094078 [GRCh38]
Chr19:36584980 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3762C>G (p.Ser1254=) single nucleotide variant not specified [RCV000611679] Chr19:36103590 [GRCh38]
Chr19:36594492 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3186C>T (p.His1062=) single nucleotide variant not specified [RCV000605687] Chr19:36102117 [GRCh38]
Chr19:36593019 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2560G>A (p.Ala854Thr) single nucleotide variant not provided [RCV000512959] Chr19:36099438 [GRCh38]
Chr19:36590340 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.922A>G (p.Ile308Val) single nucleotide variant not provided [RCV000597265] Chr19:36071595 [GRCh38]
Chr19:36562497 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2674G>A (p.Glu892Lys) single nucleotide variant not provided [RCV000513376] Chr19:36099552 [GRCh38]
Chr19:36590454 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.553G>A (p.Asp185Asn) single nucleotide variant not provided [RCV000513567] Chr19:36066419 [GRCh38]
Chr19:36557321 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2575C>T (p.Gln859Ter) single nucleotide variant Inborn genetic diseases [RCV000623794] Chr19:36099453 [GRCh38]
Chr19:36590355 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.2600G>A (p.Arg867Gln) single nucleotide variant not provided [RCV000714193] Chr19:36099478 [GRCh38]
Chr19:36590380 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1462C>T (p.Pro488Ser) single nucleotide variant not provided [RCV000714189] Chr19:36083153 [GRCh38]
Chr19:36574055 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1958+6G>C single nucleotide variant not provided [RCV000714191] Chr19:36089312 [GRCh38]
Chr19:36580214 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3368A>C (p.Gln1123Pro) single nucleotide variant not provided [RCV000714195] Chr19:36102980 [GRCh38]
Chr19:36593882 [GRCh37]
Chr19:19q13.12
uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
NM_001083961.2(WDR62):c.4153+9A>G single nucleotide variant not provided [RCV000918572] Chr19:36103990 [GRCh38]
Chr19:36594892 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1129G>T (p.Val377Leu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125023]|not provided [RCV000762011] Chr19:36073427 [GRCh38]
Chr19:36564329 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1157G>A (p.Trp386Ter) single nucleotide variant not provided [RCV000760806] Chr19:36073455 [GRCh38]
Chr19:36564357 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.1838G>T (p.Gly613Val) single nucleotide variant not provided [RCV000996851] Chr19:36089186 [GRCh38]
Chr19:36580088 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3111G>A (p.Leu1037=) single nucleotide variant not provided [RCV000981480] Chr19:36102042 [GRCh38]
Chr19:36592944 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1062G>A (p.Lys354=) single nucleotide variant not provided [RCV000959546] Chr19:36073360 [GRCh38]
Chr19:36564262 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.4236T>G (p.Leu1412=) single nucleotide variant not provided [RCV000937504] Chr19:36104600 [GRCh38]
Chr19:36595502 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2868-5T>C single nucleotide variant not provided [RCV000904799] Chr19:36101209 [GRCh38]
Chr19:36592111 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.4358C>A (p.Thr1453Asn) single nucleotide variant not provided [RCV001038018] Chr19:36104814 [GRCh38]
Chr19:36595716 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.571G>T (p.Val191Leu) single nucleotide variant not provided [RCV001038019] Chr19:36067315 [GRCh38]
Chr19:36558217 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.836G>A (p.Cys279Tyr) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001072152] Chr19:36067964 [GRCh38]
Chr19:36558866 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.75dup (p.Pro26fs) duplication Primary autosomal recessive microcephaly 2 [RCV000778544] Chr19:36055044..36055045 [GRCh38]
Chr19:36545946..36545947 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3878C>A (p.Ala1293Asp) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000778911] Chr19:36103706 [GRCh38]
Chr19:36594608 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.57C>G (p.Pro19=) single nucleotide variant not provided [RCV000927999] Chr19:36055028 [GRCh38]
Chr19:36545930 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.4209G>A (p.Pro1403=) single nucleotide variant not provided [RCV000939271] Chr19:36104573 [GRCh38]
Chr19:36595475 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1233+10C>A single nucleotide variant not provided [RCV000907135] Chr19:36073541 [GRCh38]
Chr19:36564443 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2004C>T (p.Gly668=) single nucleotide variant not provided [RCV000917308] Chr19:36090490 [GRCh38]
Chr19:36581392 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3006C>T (p.Ser1002=) single nucleotide variant not provided [RCV000895037] Chr19:36101698 [GRCh38]
Chr19:36592600 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.138G>A (p.Thr46=) single nucleotide variant not provided [RCV000980997] Chr19:36055109 [GRCh38]
Chr19:36546011 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3083-5G>A single nucleotide variant not provided [RCV000919142] Chr19:36102009 [GRCh38]
Chr19:36592911 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.312G>C (p.Gln104His) single nucleotide variant not provided [RCV000899800] Chr19:36060010 [GRCh38]
Chr19:36550912 [GRCh37]
Chr19:19q13.12
likely benign
GRCh37/hg19 19q13.11-13.12(chr19:35111811-37744992) copy number loss Generalized epilepsy with febrile seizures plus, type 1 [RCV000767768] Chr19:35111811..37744992 [GRCh37]
Chr19:19q13.11-13.12
pathogenic
NM_001083961.2(WDR62):c.561+290T>C single nucleotide variant not provided [RCV000827951] Chr19:36066717 [GRCh38]
Chr19:36557619 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1371+92T>C single nucleotide variant not provided [RCV000831580] Chr19:36081662 [GRCh38]
Chr19:36572564 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2147-13G>A single nucleotide variant not provided [RCV000828250] Chr19:36091389 [GRCh38]
Chr19:36582291 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1959-84G>C single nucleotide variant not provided [RCV000831582] Chr19:36090361 [GRCh38]
Chr19:36581263 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2035-125C>T single nucleotide variant not provided [RCV000831583] Chr19:36091075 [GRCh38]
Chr19:36581977 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2971+133G>A single nucleotide variant not provided [RCV000835852] Chr19:36101450 [GRCh38]
Chr19:36592352 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1959-33C>T single nucleotide variant not provided [RCV000837740] Chr19:36090412 [GRCh38]
Chr19:36581314 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3435T>C (p.Thr1145=) single nucleotide variant not provided [RCV000960193] Chr19:36103047 [GRCh38]
Chr19:36593949 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2521-140C>T single nucleotide variant not provided [RCV000829429] Chr19:36099259 [GRCh38]
Chr19:36590161 [GRCh37]
Chr19:19q13.12
benign
NC_000019.10:g.36091368G>A single nucleotide variant not provided [RCV000829621] Chr19:36582270 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.883-4_890del deletion Primary autosomal recessive microcephaly 2 [RCV000786042] Chr19:36071548..36071559 [GRCh38]
Chr19:36562450..36562461 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.1233+220C>T single nucleotide variant not provided [RCV000830030] Chr19:36073751 [GRCh38]
Chr19:36564653 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2334-331C>T single nucleotide variant not provided [RCV000829007] Chr19:36093700 [GRCh38]
Chr19:36584602 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.177+177C>G single nucleotide variant not provided [RCV000829420] Chr19:36055325 [GRCh38]
Chr19:36546227 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.4153+153G>T single nucleotide variant not provided [RCV000829431] Chr19:36104134 [GRCh38]
Chr19:36595036 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2210+301C>G single nucleotide variant not provided [RCV000826359] Chr19:36091766 [GRCh38]
Chr19:36582668 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.1372-10C>T single nucleotide variant not provided [RCV000827133] Chr19:36083053 [GRCh38]
Chr19:36573955 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2467+219G>A single nucleotide variant not provided [RCV000831584] Chr19:36094383 [GRCh38]
Chr19:36585285 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2740-219G>C single nucleotide variant not provided [RCV000831586] Chr19:36100529 [GRCh38]
Chr19:36591431 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.4154-162G>C single nucleotide variant not provided [RCV000831587] Chr19:36104356 [GRCh38]
Chr19:36595258 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.1684C>G (p.His562Asp) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV000786041] Chr19:36086728 [GRCh38]
Chr19:36577630 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.2971+138C>T single nucleotide variant not provided [RCV000836450] Chr19:36101455 [GRCh38]
Chr19:36592357 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.562-335G>A single nucleotide variant not provided [RCV000826358] Chr19:36066971 [GRCh38]
Chr19:36557873 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2739+173G>A single nucleotide variant not provided [RCV000837020] Chr19:36099790 [GRCh38]
Chr19:36590692 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.1233+7C>A single nucleotide variant not provided [RCV000996850] Chr19:36073538 [GRCh38]
Chr19:36564440 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2035-115T>C single nucleotide variant not provided [RCV000829425] Chr19:36091085 [GRCh38]
Chr19:36581987 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2211-168del deletion not provided [RCV000829426] Chr19:36092521 [GRCh38]
Chr19:36583423 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.3082+76G>T single nucleotide variant not provided [RCV000829622] Chr19:36101850 [GRCh38]
Chr19:36592752 [GRCh37]
Chr19:19q13.12
benign
NC_000019.10:g.36086648G>A single nucleotide variant not provided [RCV000833253] Chr19:36577550 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2467+46_2467+47del deletion not provided [RCV000833254] Chr19:36094210..36094211 [GRCh38]
Chr19:36585112..36585113 [GRCh37]
Chr19:19q13.12
benign
NC_000019.10:g.36094002C>T single nucleotide variant not provided [RCV000833281] Chr19:36584904 [GRCh37]
Chr19:19q13.12
benign
NC_000019.10:g.36086840G>A single nucleotide variant not provided [RCV000829620] Chr19:36577742 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.1550+306G>A single nucleotide variant not provided [RCV000827952] Chr19:36083547 [GRCh38]
Chr19:36574449 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2210+280C>T single nucleotide variant not provided [RCV000830492] Chr19:36091745 [GRCh38]
Chr19:36582647 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.391-10C>T single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122246]|not provided [RCV000829200] Chr19:36066247 [GRCh38]
Chr19:36557149 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.883-166G>A single nucleotide variant not provided [RCV000829422] Chr19:36071390 [GRCh38]
Chr19:36562292 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.1550+218A>G single nucleotide variant not provided [RCV000829423] Chr19:36083459 [GRCh38]
Chr19:36574361 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2334-152G>A single nucleotide variant not provided [RCV000829427] Chr19:36093879 [GRCh38]
Chr19:36584781 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.562-324G>C single nucleotide variant not provided [RCV000830490] Chr19:36066982 [GRCh38]
Chr19:36557884 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2739+125A>G single nucleotide variant not provided [RCV000837330] Chr19:36099742 [GRCh38]
Chr19:36590644 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.562-95T>C single nucleotide variant not provided [RCV000829421] Chr19:36067211 [GRCh38]
Chr19:36558113 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.1768+220G>A single nucleotide variant not provided [RCV000829424] Chr19:36087032 [GRCh38]
Chr19:36577934 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2467+108G>A single nucleotide variant not provided [RCV000829428] Chr19:36094272 [GRCh38]
Chr19:36585174 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.2740-234A>G single nucleotide variant not provided [RCV000829430] Chr19:36100514 [GRCh38]
Chr19:36591416 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.1550+141C>A single nucleotide variant not provided [RCV000831581] Chr19:36083382 [GRCh38]
Chr19:36574284 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2521-133G>A single nucleotide variant not provided [RCV000831585] Chr19:36099266 [GRCh38]
Chr19:36590168 [GRCh37]
Chr19:19q13.12
benign
NC_000019.10:g.36103251G>A single nucleotide variant not provided [RCV000829623] Chr19:36594153 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.669del (p.Trp224fs) deletion Primary autosomal recessive microcephaly 2 [RCV001009331] Chr19:36067413 [GRCh38]
Chr19:36558315 [GRCh37]
Chr19:19q13.12
pathogenic
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3 copy number gain not provided [RCV000845733] Chr19:28271106..49213832 [GRCh37]
Chr19:19q11-13.33
pathogenic
NM_001083961.2(WDR62):c.4020C>T (p.His1340=) single nucleotide variant not provided [RCV000914090] Chr19:36103848 [GRCh38]
Chr19:36594750 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.4283T>C (p.Phe1428Ser) single nucleotide variant Microcephaly [RCV000850356]|Primary autosomal recessive microcephaly 2 [RCV001128276] Chr19:36104647 [GRCh38]
Chr19:36595549 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1212del (p.Ser405fs) deletion not provided [RCV001008494] Chr19:36073510 [GRCh38]
Chr19:36564412 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.4234dup (p.Leu1412fs) duplication not provided [RCV001009224] Chr19:36104594..36104595 [GRCh38]
Chr19:36595496..36595497 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.1031G>A (p.Gly344Asp) single nucleotide variant not provided [RCV001171704] Chr19:36071704 [GRCh38]
Chr19:36562606 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1821dup (p.Arg608fs) duplication Primary autosomal recessive microcephaly 2 [RCV001255785]|not provided [RCV001008125] Chr19:36089087..36089088 [GRCh38]
Chr19:36579989..36579990 [GRCh37]
Chr19:19q13.12
pathogenic
GRCh37/hg19 19q13.12(chr19:36570287-36655341)x3 copy number gain not provided [RCV000846132] Chr19:36570287..36655341 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.159G>A (p.Glu53=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128004] Chr19:36055130 [GRCh38]
Chr19:36546032 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.803G>C (p.Ser268Thr) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122249] Chr19:36067931 [GRCh38]
Chr19:36558833 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1709A>G (p.Tyr570Cys) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122352] Chr19:36086753 [GRCh38]
Chr19:36577655 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1837-12C>T single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122354] Chr19:36089173 [GRCh38]
Chr19:36580075 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2728C>A (p.Leu910Met) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001196088] Chr19:36099606 [GRCh38]
Chr19:36590508 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1218C>T (p.Tyr406=) single nucleotide variant not provided [RCV000967509] Chr19:36073516 [GRCh38]
Chr19:36564418 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3108G>A (p.Glu1036=) single nucleotide variant not provided [RCV000967510] Chr19:36102039 [GRCh38]
Chr19:36592941 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1695C>T (p.Asn565=) single nucleotide variant not provided [RCV000923750] Chr19:36086739 [GRCh38]
Chr19:36577641 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1768+9C>T single nucleotide variant not provided [RCV000902034] Chr19:36086821 [GRCh38]
Chr19:36577723 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.270-9T>C single nucleotide variant not provided [RCV000916451] Chr19:36059959 [GRCh38]
Chr19:36550861 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2624C>T (p.Thr875Ile) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126113] Chr19:36099502 [GRCh38]
Chr19:36590404 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2814T>C (p.Ser938=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126114] Chr19:36100822 [GRCh38]
Chr19:36591724 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.272G>A (p.Cys91Tyr) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128007] Chr19:36059970 [GRCh38]
Chr19:36550872 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3587C>T (p.Thr1196Met) single nucleotide variant not provided [RCV001227803] Chr19:36103415 [GRCh38]
Chr19:36594317 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.824C>T (p.Ser275Leu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125020] Chr19:36067952 [GRCh38]
Chr19:36558854 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3514C>T (p.Pro1172Ser) single nucleotide variant not provided [RCV000993554] Chr19:36103207 [GRCh38]
Chr19:36594109 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.303C>T (p.Asn101=) single nucleotide variant not provided [RCV000911420] Chr19:36060001 [GRCh38]
Chr19:36550903 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.2376G>C (p.Leu792=) single nucleotide variant not provided [RCV000889384] Chr19:36094073 [GRCh38]
Chr19:36584975 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.4012A>C (p.Arg1338=) single nucleotide variant not provided [RCV000911706] Chr19:36103840 [GRCh38]
Chr19:36594742 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3063G>A (p.Thr1021=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128203]|not provided [RCV000912973] Chr19:36101755 [GRCh38]
Chr19:36592657 [GRCh37]
Chr19:19q13.12
likely benign|uncertain significance
NM_001083961.2(WDR62):c.4033C>T (p.Arg1345Cys) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126222]|not provided [RCV000891068] Chr19:36103861 [GRCh38]
Chr19:36594763 [GRCh37]
Chr19:19q13.12
benign|likely benign|conflicting interpretations of pathogenicity
NM_001083961.2(WDR62):c.4402G>A (p.Ala1468Thr) single nucleotide variant Intellectual disability [RCV001263362] Chr19:36104858 [GRCh38]
Chr19:36595760 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4464_4471dup (p.Pro1491fs) duplication not provided [RCV001008995] Chr19:36104918..36104919 [GRCh38]
Chr19:36595820..36595821 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.2950A>G (p.Lys984Glu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128199] Chr19:36101296 [GRCh38]
Chr19:36592198 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.*57G>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125355] Chr19:36105085 [GRCh38]
Chr19:36595987 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.121T>A (p.Cys41Ser) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125901]|Seizures [RCV001255102] Chr19:36055092 [GRCh38]
Chr19:36545994 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1233+11C>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126006] Chr19:36073542 [GRCh38]
Chr19:36564444 [GRCh37]
Chr19:19q13.12
benign
NM_001083961.2(WDR62):c.3221-13G>T single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122468] Chr19:36102724 [GRCh38]
Chr19:36593626 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.546C>T (p.Asn182=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122247] Chr19:36066412 [GRCh38]
Chr19:36557314 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1836+15C>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122353] Chr19:36089120 [GRCh38]
Chr19:36580022 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3874G>A (p.Glu1292Lys) single nucleotide variant not provided [RCV001092331] Chr19:36103702 [GRCh38]
Chr19:36594604 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2520+5G>T single nucleotide variant Intellectual disability [RCV001291204]|not provided [RCV001235711] Chr19:36097084 [GRCh38]
Chr19:36587986 [GRCh37]
Chr19:19q13.12
pathogenic|likely pathogenic
NM_001083961.2(WDR62):c.390+1G>T single nucleotide variant not provided [RCV001235712] Chr19:36066016 [GRCh38]
Chr19:36556918 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.4345C>T (p.Gln1449Ter) single nucleotide variant not provided [RCV001171705] Chr19:36104801 [GRCh38]
Chr19:36595703 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.892T>C (p.Ser298Pro) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125021] Chr19:36071565 [GRCh38]
Chr19:36562467 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3221-15G>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122467] Chr19:36102722 [GRCh38]
Chr19:36593624 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.64A>C (p.Met22Leu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125900] Chr19:36055035 [GRCh38]
Chr19:36545937 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1233+15C>A single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126007] Chr19:36073546 [GRCh38]
Chr19:36564448 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.3857G>A (p.Arg1286His) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126220] Chr19:36103685 [GRCh38]
Chr19:36594587 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.3950C>T (p.Pro1317Leu) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001126221] Chr19:36103778 [GRCh38]
Chr19:36594680 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2788C>T (p.Gln930Ter) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001007663] Chr19:36100796 [GRCh38]
Chr19:36591698 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.241G>A (p.Gly81Ser) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128006] Chr19:36058843 [GRCh38]
Chr19:36549745 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.328G>A (p.Ala110Thr) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001128008] Chr19:36060026 [GRCh38]
Chr19:36550928 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.984C>T (p.Leu328=) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125022] Chr19:36071657 [GRCh38]
Chr19:36562559 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.1183G>A (p.Gly395Ser) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125024] Chr19:36073481 [GRCh38]
Chr19:36564383 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2334-13T>C single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001125143] Chr19:36094018 [GRCh38]
Chr19:36584920 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2000A>G (p.Lys667Arg) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001122355] Chr19:36090486 [GRCh38]
Chr19:36581388 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.4312-1G>C single nucleotide variant Intellectual disability [RCV001255365]|Primary autosomal recessive microcephaly 2 [RCV001262828] Chr19:36104767 [GRCh38]
Chr19:36595669 [GRCh37]
Chr19:19q13.12
pathogenic|uncertain significance
NM_001083961.2(WDR62):c.1576G>T (p.Glu526Ter) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001253709] Chr19:36084678 [GRCh38]
Chr19:36575580 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.118A>G (p.Ile40Val) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001255791] Chr19:36055089 [GRCh38]
Chr19:36545991 [GRCh37]
Chr19:19q13.12
likely benign
NM_001083961.2(WDR62):c.1963dup (p.Tyr655fs) duplication Primary autosomal recessive microcephaly 2 [RCV001255843] Chr19:36090448..36090449 [GRCh38]
Chr19:36581350..36581351 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.2588G>A (p.Arg863His) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001255756] Chr19:36099466 [GRCh38]
Chr19:36590368 [GRCh37]
Chr19:19q13.12
pathogenic
NM_001083961.2(WDR62):c.2765G>A (p.Arg922His) single nucleotide variant Global developmental delay [RCV001256136] Chr19:36100773 [GRCh38]
Chr19:36591675 [GRCh37]
Chr19:19q13.12
uncertain significance
NM_001083961.2(WDR62):c.2486C>T (p.Thr829Ile) single nucleotide variant Primary autosomal recessive microcephaly 2 [RCV001255769] Chr19:36097045 [GRCh38]
Chr19:36587947 [GRCh37]
Chr19:19q13.12
likely pathogenic
NM_001083961.2(WDR62):c.1973_1974del (p.Val658fs) microsatellite not provided [RCV001269841] Chr19:36090457..36090458 [GRCh38]
Chr19:36581359..36581360 [GRCh37]
Chr19:19q13.12
likely pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:24502 AgrOrtholog
COSMIC WDR62 COSMIC
Ensembl Genes ENSG00000075702 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000270301 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000384792 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000413475 UniProtKB/TrEMBL
  ENSP00000465525 UniProtKB/Swiss-Prot
  ENSP00000494253 UniProtKB/TrEMBL
  ENSP00000505158 ENTREZGENE
  ENSP00000505582 ENTREZGENE
  ENSP00000506226 ENTREZGENE
Ensembl Transcript ENST00000270301 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000401500 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000427823 UniProtKB/TrEMBL
  ENST00000587391 UniProtKB/Swiss-Prot
  ENST00000644764 UniProtKB/TrEMBL
  ENST00000679682 ENTREZGENE
  ENST00000679757 ENTREZGENE
  ENST00000680564 ENTREZGENE
Gene3D-CATH 2.130.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000075702 GTEx
HGNC ID HGNC:24502 ENTREZGENE
Human Proteome Map WDR62 Human Proteome Map
InterPro Apc4_WD40_dom UniProtKB/Swiss-Prot
  Quinoprotein_ADH-like_supfam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40/YVTN_repeat-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:284403 UniProtKB/Swiss-Prot
NCBI Gene 284403 ENTREZGENE
OMIM 604317 OMIM
  613583 OMIM
Pfam ANAPC4_WD40 UniProtKB/Swiss-Prot
  WD40 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134963627 PharmGKB
PROSITE WD_REPEATS_2 UniProtKB/Swiss-Prot
  WD_REPEATS_REGION UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART WD40 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50978 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF50998 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0S2SW22_HUMAN UniProtKB/TrEMBL
  A0A0S2Z5Z6_HUMAN UniProtKB/TrEMBL
  A0A0S2Z606_HUMAN UniProtKB/TrEMBL
  A0A0S2Z635_HUMAN UniProtKB/TrEMBL
  A0A2R8YD43_HUMAN UniProtKB/TrEMBL
  H7C3R4_HUMAN UniProtKB/TrEMBL
  O43379 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary Q63HP9 UniProtKB/Swiss-Prot
  Q659D7 UniProtKB/Swiss-Prot
  Q8NBF7 UniProtKB/Swiss-Prot
  Q96AD9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-22 WDR62  WD repeat domain 62  MCPH2  microcephaly, primary autosomal recessive 2  Data Merged 737654 PROVISIONAL
2011-08-17 WDR62  WD repeat domain 62  WDR62  WD repeat domain 62  Symbol and/or name change 5135510 APPROVED
2011-07-27 WDR62  WD repeat domain 62  WDR62  WD repeat domain 62  Symbol and/or name change 5135510 APPROVED