GPC6 (glypican 6) - Rat Genome Database

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Gene: GPC6 (glypican 6) Homo sapiens
Analyze
Symbol: GPC6
Name: glypican 6
RGD ID: 1352914
HGNC Page HGNC:4454
Description: Predicted to enable coreceptor activity. Involved in cell migration. Located in nucleus. Implicated in omodysplasia 1.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: glypican proteoglycan 6; glypican-6; MGC126288; OMIMD1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381393,216,529 - 94,408,020 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1393,226,807 - 94,408,020 (+)EnsemblGRCh38hg38GRCh38
GRCh371393,879,060 - 95,060,274 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361392,677,096 - 93,853,948 (+)NCBINCBI36Build 36hg18NCBI36
Build 341392,677,095 - 93,853,948NCBI
Celera1374,727,460 - 75,908,516 (+)NCBICelera
Cytogenetic Map13q31.3-q32.1NCBI
HuRef1374,476,112 - 75,657,237 (+)NCBIHuRef
CHM1_11393,848,682 - 95,029,827 (+)NCBICHM1_1
T2T-CHM13v2.01392,430,763 - 93,611,616 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(1->4)-beta-D-glucan  (ISO)
1,2-dichloroethane  (ISO)
17beta-estradiol  (EXP)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dibromophenyl 2,4,5-tribromophenyl ether  (ISO)
3,3',4,4',5-pentachlorobiphenyl  (EXP)
4,4'-sulfonyldiphenol  (EXP)
5-aza-2'-deoxycytidine  (EXP)
6-propyl-2-thiouracil  (ISO)
7,12-dimethyltetraphene  (ISO)
aflatoxin B1  (EXP)
Aflatoxin B2 alpha  (EXP)
all-trans-retinoic acid  (EXP)
aristolochic acid A  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
atrazine  (EXP,ISO)
belinostat  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
butanal  (EXP)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
calcitriol  (EXP)
cannabidiol  (ISO)
carbamazepine  (EXP)
CGP 52608  (EXP)
cisplatin  (EXP)
clothianidin  (EXP)
copper(II) chloride  (EXP)
Cuprizon  (ISO)
cyclosporin A  (EXP)
D-mannitol  (ISO)
dexamethasone  (EXP)
diarsenic trioxide  (EXP)
diethylstilbestrol  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
entinostat  (EXP)
ethanol  (ISO)
fulvestrant  (EXP)
gentamycin  (ISO)
Lasiocarpine  (EXP)
lead(0)  (EXP)
leflunomide  (EXP)
lipopolysaccharide  (EXP)
N,N-diethyl-m-toluamide  (ISO)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
O-methyleugenol  (EXP)
panobinostat  (EXP)
paracetamol  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
permethrin  (ISO)
phenobarbital  (ISO)
potassium chromate  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium arsenate  (ISO)
sodium arsenite  (EXP,ISO)
sodium fluoride  (ISO)
sunitinib  (EXP)
testosterone  (EXP)
tetrachloromethane  (ISO)
titanium dioxide  (ISO)
tributylstannane  (ISO)
trichostatin A  (EXP)
valproic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
6. Dally-like core protein and its mammalian homologues mediate stimulatory and inhibitory effects on Hedgehog signal response. Williams EH, etal., Proc Natl Acad Sci U S A. 2010 Mar 30;107(13):5869-74. Epub 2010 Mar 15.
Additional References at PubMed
PMID:7657705   PMID:10329016   PMID:10480909   PMID:12477932   PMID:12975309   PMID:15057823   PMID:15489334   PMID:16344560   PMID:17903302   PMID:18839057   PMID:19481194   PMID:19726429  
PMID:19834535   PMID:20379614   PMID:20634892   PMID:20692050   PMID:20889312   PMID:21630459   PMID:21871017   PMID:21873635   PMID:22044751   PMID:22589738   PMID:22747683   PMID:22993228  
PMID:23251661   PMID:23535033   PMID:24159190   PMID:24431302   PMID:24554482   PMID:24804215   PMID:25189868   PMID:25624497   PMID:26186194   PMID:26448945   PMID:27609421   PMID:28077445  
PMID:28514442   PMID:29162697   PMID:29180619   PMID:29509190   PMID:29845934   PMID:31111662   PMID:31199813   PMID:32478377   PMID:32707033   PMID:33094648   PMID:33187986   PMID:33762006  
PMID:33961781   PMID:35271311   PMID:36165234   PMID:36215168   PMID:37353964   PMID:38697112  


Genomics

Comparative Map Data
GPC6
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381393,216,529 - 94,408,020 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1393,226,807 - 94,408,020 (+)EnsemblGRCh38hg38GRCh38
GRCh371393,879,060 - 95,060,274 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361392,677,096 - 93,853,948 (+)NCBINCBI36Build 36hg18NCBI36
Build 341392,677,095 - 93,853,948NCBI
Celera1374,727,460 - 75,908,516 (+)NCBICelera
Cytogenetic Map13q31.3-q32.1NCBI
HuRef1374,476,112 - 75,657,237 (+)NCBIHuRef
CHM1_11393,848,682 - 95,029,827 (+)NCBICHM1_1
T2T-CHM13v2.01392,430,763 - 93,611,616 (+)NCBIT2T-CHM13v2.0
Gpc6
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3914117,162,332 - 118,216,941 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl14117,162,727 - 118,213,956 (+)EnsemblGRCm39 Ensembl
GRCm3814116,924,920 - 117,979,529 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl14116,925,315 - 117,976,544 (+)EnsemblGRCm38mm10GRCm38
MGSCv3714117,324,537 - 118,378,751 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3614115,808,387 - 116,859,339 (+)NCBIMGSCv36mm8
Celera14115,484,341 - 116,531,683 (+)NCBICelera
Cytogenetic Map14E4NCBI
cM Map1460.34NCBI
Gpc6
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr815100,437,415 - 101,435,038 (+)NCBIGRCr8
mRatBN7.21594,030,218 - 95,027,883 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1594,029,884 - 95,024,006 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.015102,164,091 - 103,174,721 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl15102,164,751 - 103,170,847 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.015105,607,785 - 106,611,654 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.415101,763,223 - 102,656,127 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1592,888,323 - 93,881,886 (+)NCBICelera
Cytogenetic Map15q24NCBI
Gpc6
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540415,433,962 - 16,504,351 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495540415,429,811 - 16,504,973 (-)NCBIChiLan1.0ChiLan1.0
GPC6
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21494,764,666 - 95,943,637 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11393,433,119 - 94,612,958 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01374,408,999 - 75,588,065 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11393,556,152 - 94,744,052 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1393,874,849 - 94,739,894 (+)Ensemblpanpan1.1panPan2
GPC6
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12244,154,690 - 45,237,398 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2244,154,944 - 45,233,549 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2244,008,265 - 45,024,162 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02244,583,937 - 45,667,974 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2244,584,263 - 45,667,325 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12244,239,373 - 45,321,705 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02244,280,456 - 45,362,460 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02244,290,207 - 45,372,251 (+)NCBIUU_Cfam_GSD_1.0
Gpc6
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404945179,774,517 - 180,818,680 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647215,137,770 - 16,176,943 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647215,136,656 - 16,177,597 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
GPC6
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1162,438,453 - 63,560,897 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11162,436,143 - 63,560,908 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
GPC6
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1372,075,622 - 73,242,678 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604628,496,652 - 29,624,562 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Gpc6
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462487997,257 - 1,192,604 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462487997,125 - 1,196,747 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in GPC6
332 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_005708.5(GPC6):c.778del (p.Leu260fs) deletion Autosomal recessive omodysplasia [RCV000005888] Chr13:94027795 [GRCh38]
Chr13:94680049 [GRCh37]
Chr13:13q31.3
pathogenic
NC_000013.11:g.93997007_94063501del66495insATAAATCACTTAGAGATGT indel Autosomal recessive omodysplasia [RCV000005889] Chr13:93997007..94063501 [GRCh38]
Chr13:94649261..94715755 [GRCh37]
Chr13:93447262..93513756 [NCBI36]
Chr13:13q31.3
pathogenic
NC_000013.11:g.94252984_94352299del99316insCTA indel Autosomal recessive omodysplasia [RCV000005890] Chr13:94252984..94352299 [GRCh38]
Chr13:94905238..95004553 [GRCh37]
Chr13:93703239..93802554 [NCBI36]
Chr13:13q31.3
pathogenic
NM_005708.3(GPC6):c.712_877dup duplication Autosomal recessive omodysplasia [RCV000005892] Chr13:94011504..94038749 [GRCh38]
Chr13:13q31.3
pathogenic
NM_005708.3(GPC6):c.320_711del deletion Autosomal recessive omodysplasia [RCV000005893] Chr13:93741318..93830948 [GRCh38]
Chr13:94393571..94483201 [GRCh37]
Chr13:13q32
pathogenic
NM_005708.3(GPC6):c.320_711del deletion Autosomal recessive omodysplasia [RCV000005894] Chr13:93603313..93860330 [GRCh38]
Chr13:94255566..94512583 [GRCh37]
Chr13:13q31.3
pathogenic
NM_005708.5(GPC6):c.700C>T (p.Arg234Ter) single nucleotide variant Autosomal recessive omodysplasia [RCV000005891] Chr13:93830534 [GRCh38]
Chr13:94482787 [GRCh37]
Chr13:13q31.3
pathogenic
NM_005708.3(GPC6):c.160+41083A>G single nucleotide variant Lung cancer [RCV000098467] Chr13:93268699 [GRCh38]
Chr13:93920952 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.160+110112T>A single nucleotide variant Lung cancer [RCV000098468] Chr13:93337728 [GRCh38]
Chr13:93989981 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.161-135739A>T single nucleotide variant Lung cancer [RCV000098469] Chr13:93409524 [GRCh38]
Chr13:94061777 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.319+84988A>T single nucleotide variant Lung cancer [RCV000098470] Chr13:93630409 [GRCh38]
Chr13:94282662 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.319+98048A>G single nucleotide variant Lung cancer [RCV000098471] Chr13:93643469 [GRCh38]
Chr13:94295722 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.320-130340G>C single nucleotide variant Lung cancer [RCV000098472] Chr13:93699814 [GRCh38]
Chr13:94352067 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.320-128094A>G single nucleotide variant Lung cancer [RCV000098473] Chr13:93702060 [GRCh38]
Chr13:94354313 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.320-71049A>T single nucleotide variant Lung cancer [RCV000098474] Chr13:93759105 [GRCh38]
Chr13:94411358 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.320-61489C>G single nucleotide variant Lung cancer [RCV000098475] Chr13:93768665 [GRCh38]
Chr13:94420918 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.878-88923C>A single nucleotide variant Lung cancer [RCV000098476] Chr13:94197426 [GRCh38]
Chr13:94849680 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.878-12747A>C single nucleotide variant Lung cancer [RCV000098477] Chr13:94273602 [GRCh38]
Chr13:94925856 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.1009-9467G>T single nucleotide variant Lung cancer [RCV000098478] Chr13:94296513 [GRCh38]
Chr13:94948767 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.3(GPC6):c.1153-36570T>A single nucleotide variant Lung cancer [RCV000098479] Chr13:94345844 [GRCh38]
Chr13:94998098 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh38/hg38 13q22.3-32.1(chr13:78349126-94701844)x1 copy number loss See cases [RCV000051379] Chr13:78349126..94701844 [GRCh38]
Chr13:78923261..95354098 [GRCh37]
Chr13:77821262..94152099 [NCBI36]
Chr13:13q22.3-32.1
pathogenic
GRCh38/hg38 13q31.1-32.1(chr13:83947821-95128969)x1 copy number loss See cases [RCV000051414] Chr13:83947821..95128969 [GRCh38]
Chr13:84521956..95781223 [GRCh37]
Chr13:83419957..94579224 [NCBI36]
Chr13:13q31.1-32.1
pathogenic
GRCh38/hg38 13q31.2-32.1(chr13:88260962-97285754)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051415]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051415]|See cases [RCV000051415] Chr13:88260962..97285754 [GRCh38]
Chr13:88913217..97938008 [GRCh37]
Chr13:87711218..96736009 [NCBI36]
Chr13:13q31.2-32.1
pathogenic
GRCh38/hg38 13q31.2-32.3(chr13:88323009-98888644)x1 copy number loss See cases [RCV000051416] Chr13:88323009..98888644 [GRCh38]
Chr13:88975264..99540898 [GRCh37]
Chr13:87773265..98338899 [NCBI36]
Chr13:13q31.2-32.3
pathogenic
GRCh38/hg38 13q31.3-32.1(chr13:89549510-96657834)x1 copy number loss See cases [RCV000051417] Chr13:89549510..96657834 [GRCh38]
Chr13:90201764..97310088 [GRCh37]
Chr13:88999765..96108089 [NCBI36]
Chr13:13q31.3-32.1
pathogenic
GRCh38/hg38 13q31.3-34(chr13:91366227-114327314)x1 copy number loss See cases [RCV000051418] Chr13:91366227..114327314 [GRCh38]
Chr13:92018481..115085141 [GRCh37]
Chr13:90816482..114110891 [NCBI36]
Chr13:13q31.3-34
pathogenic
GRCh38/hg38 13q31.3-32.1(chr13:93571649-97428965)x1 copy number loss See cases [RCV000051419] Chr13:93571649..97428965 [GRCh38]
Chr13:94223902..98081219 [GRCh37]
Chr13:93021903..96879220 [NCBI36]
Chr13:13q31.3-32.1
pathogenic
GRCh38/hg38 13q31.1-33.2(chr13:82032938-106082542)x3 copy number gain See cases [RCV000051179] Chr13:82032938..106082542 [GRCh38]
Chr13:82607073..106734891 [GRCh37]
Chr13:81505074..105532892 [NCBI36]
Chr13:13q31.1-33.2
pathogenic
GRCh38/hg38 13q31.3(chr13:93345058-93629454)x1 copy number loss See cases [RCV000051924] Chr13:93345058..93629454 [GRCh38]
Chr13:93997311..94281707 [GRCh37]
Chr13:92795312..93079708 [NCBI36]
Chr13:13q31.3
uncertain significance
GRCh38/hg38 13q31.1-34(chr13:82581008-114327173)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051380]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051380]|See cases [RCV000051380] Chr13:82581008..114327173 [GRCh38]
Chr13:83155143..115085141 [GRCh37]
Chr13:82053144..114110750 [NCBI36]
Chr13:13q31.1-34
pathogenic
GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3 copy number gain See cases [RCV000053731] Chr13:19837395..114327173 [GRCh38]
Chr13:20411535..115085141 [GRCh37]
Chr13:19309535..114110750 [NCBI36]
Chr13:13q12.11-34
pathogenic
GRCh38/hg38 13q11-34(chr13:18565048-114327173)x3 copy number gain See cases [RCV000053719] Chr13:18565048..114327173 [GRCh38]
Chr13:19139188..115085141 [GRCh37]
Chr13:18037188..114110750 [NCBI36]
Chr13:13q11-34
pathogenic
GRCh38/hg38 13q11-34(chr13:18850545-114327173)x3 copy number gain See cases [RCV000053723] Chr13:18850545..114327173 [GRCh38]
Chr13:19296527..115085141 [GRCh37]
Chr13:18194527..114110750 [NCBI36]
Chr13:13q11-34
pathogenic
GRCh38/hg38 13q12.11-34(chr13:18946182-114304628)x3 copy number gain See cases [RCV000053726] Chr13:18946182..114304628 [GRCh38]
Chr13:19520322..115070103 [GRCh37]
Chr13:18418322..114088205 [NCBI36]
Chr13:13q12.11-34
pathogenic
GRCh38/hg38 13q13.2-34(chr13:33528097-114327173)x3 copy number gain See cases [RCV000053759] Chr13:33528097..114327173 [GRCh38]
Chr13:34102234..115085141 [GRCh37]
Chr13:33000234..114110750 [NCBI36]
Chr13:13q13.2-34
pathogenic
GRCh38/hg38 13q31.3-33.1(chr13:93213623-101537104)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053790]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053790]|See cases [RCV000053790] Chr13:93213623..101537104 [GRCh38]
Chr13:93865876..102189455 [GRCh37]
Chr13:92663877..100987456 [NCBI36]
Chr13:13q31.3-33.1
pathogenic
GRCh38/hg38 13q14.11-34(chr13:43219125-114327314)x3 copy number gain See cases [RCV000053762] Chr13:43219125..114327314 [GRCh38]
Chr13:43793261..115085141 [GRCh37]
Chr13:42691261..114110891 [NCBI36]
Chr13:13q14.11-34
pathogenic
GRCh38/hg38 13q14.11-34(chr13:44164751-114327173)x3 copy number gain See cases [RCV000053764] Chr13:44164751..114327173 [GRCh38]
Chr13:44738887..115085141 [GRCh37]
Chr13:43636887..114110750 [NCBI36]
Chr13:13q14.11-34
pathogenic
GRCh38/hg38 13q14.12-34(chr13:44733046-114327173)x3 copy number gain See cases [RCV000053767] Chr13:44733046..114327173 [GRCh38]
Chr13:45307182..115085141 [GRCh37]
Chr13:44205182..114110750 [NCBI36]
Chr13:13q14.12-34
pathogenic
GRCh38/hg38 13q22.1-34(chr13:74345951-114327314)x3 copy number gain See cases [RCV000053770] Chr13:74345951..114327314 [GRCh38]
Chr13:74920088..115085141 [GRCh37]
Chr13:73818089..114110891 [NCBI36]
Chr13:13q22.1-34
pathogenic
GRCh38/hg38 13q31.1-34(chr13:80628584-114327173)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053772]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053772]|See cases [RCV000053772] Chr13:80628584..114327173 [GRCh38]
Chr13:81202719..115085141 [GRCh37]
Chr13:80100720..114110750 [NCBI36]
Chr13:13q31.1-34
pathogenic
GRCh38/hg38 13q12.11-34(chr13:19833130-114298614)x3 copy number gain See cases [RCV000134104] Chr13:19833130..114298614 [GRCh38]
Chr13:20407270..115064089 [GRCh37]
Chr13:19305270..114082191 [NCBI36]
Chr13:13q12.11-34
pathogenic
GRCh38/hg38 13q31.3-32.1(chr13:93908109-94449189)x3 copy number gain See cases [RCV000135798] Chr13:93908109..94449189 [GRCh38]
Chr13:94560362..95101443 [GRCh37]
Chr13:93358363..93899444 [NCBI36]
Chr13:13q31.3-32.1
uncertain significance
GRCh38/hg38 13q31.2-34(chr13:88937651-114327173)x3 copy number gain See cases [RCV000137102] Chr13:88937651..114327173 [GRCh38]
Chr13:89589905..115085141 [GRCh37]
Chr13:88387906..114110750 [NCBI36]
Chr13:13q31.2-34
pathogenic
GRCh38/hg38 13q31.3-33.3(chr13:93345058-109458154)x1 copy number loss See cases [RCV000136688] Chr13:93345058..109458154 [GRCh38]
Chr13:93997311..110110501 [GRCh37]
Chr13:92795312..108908502 [NCBI36]
Chr13:13q31.3-33.3
pathogenic
GRCh38/hg38 13q14.11-34(chr13:40942298-114340331)x1 copy number loss See cases [RCV000137893] Chr13:40942298..114340331 [GRCh38]
Chr13:41516434..115085141 [GRCh37]
Chr13:40414434..114123908 [NCBI36]
Chr13:13q14.11-34
pathogenic
GRCh38/hg38 13q31.3(chr13:92695363-93634680)x1 copy number loss See cases [RCV000137885] Chr13:92695363..93634680 [GRCh38]
Chr13:93347616..94286933 [GRCh37]
Chr13:92145617..93084934 [NCBI36]
Chr13:13q31.3
uncertain significance
GRCh38/hg38 13q31.1-34(chr13:78999318-114327106)x3 copy number gain See cases [RCV000138742] Chr13:78999318..114327106 [GRCh38]
Chr13:79573453..115085141 [GRCh37]
Chr13:78471454..114110683 [NCBI36]
Chr13:13q31.1-34
pathogenic
GRCh38/hg38 13q31.3(chr13:93383656-93538852)x1 copy number loss See cases [RCV000138761] Chr13:93383656..93538852 [GRCh38]
Chr13:94035909..94191105 [GRCh37]
Chr13:92833910..92989106 [NCBI36]
Chr13:13q31.3
likely benign
GRCh38/hg38 13q31.1-34(chr13:86788927-114340331)x1 copy number loss See cases [RCV000138340] Chr13:86788927..114340331 [GRCh38]
Chr13:87441182..115085141 [GRCh37]
Chr13:86239183..114123908 [NCBI36]
Chr13:13q31.1-34
pathogenic
GRCh38/hg38 13q12.11-34(chr13:19833130-114327106)x3 copy number gain See cases [RCV000139078] Chr13:19833130..114327106 [GRCh38]
Chr13:20407270..115085141 [GRCh37]
Chr13:19305270..114110683 [NCBI36]
Chr13:13q12.11-34
pathogenic
GRCh38/hg38 13q31.2-32.3(chr13:87944479-99866542)x1 copy number loss See cases [RCV000139047] Chr13:87944479..99866542 [GRCh38]
Chr13:88596734..100518796 [GRCh37]
Chr13:87394735..99316797 [NCBI36]
Chr13:13q31.2-32.3
pathogenic
GRCh38/hg38 13q31.3(chr13:93689856-93770897)x3 copy number gain See cases [RCV000139970] Chr13:93689856..93770897 [GRCh38]
Chr13:94342109..94423150 [GRCh37]
Chr13:93140110..93221151 [NCBI36]
Chr13:13q31.3
benign
GRCh38/hg38 13q11-34(chr13:18456040-114340285)x3 copy number gain See cases [RCV000140004] Chr13:18456040..114340285 [GRCh38]
Chr13:19030180..115105760 [GRCh37]
Chr13:17928180..114123862 [NCBI36]
Chr13:13q11-34
pathogenic
GRCh38/hg38 13q31.1-34(chr13:78964223-114340331)x3 copy number gain See cases [RCV000141248] Chr13:78964223..114340331 [GRCh38]
Chr13:79538358..115085141 [GRCh37]
Chr13:78436359..114123908 [NCBI36]
Chr13:13q31.1-34
pathogenic
GRCh38/hg38 13q31.3-32.1(chr13:93869283-94459255)x3 copy number gain See cases [RCV000141918] Chr13:93869283..94459255 [GRCh38]
Chr13:94521536..95111509 [GRCh37]
Chr13:93319537..93909510 [NCBI36]
Chr13:13q31.3-32.1
uncertain significance
GRCh38/hg38 13q31.3(chr13:93601411-93624805)x1 copy number loss See cases [RCV000141507] Chr13:93601411..93624805 [GRCh38]
Chr13:94253664..94277058 [GRCh37]
Chr13:93051665..93075059 [NCBI36]
Chr13:13q31.3
benign
GRCh38/hg38 13q31.1-34(chr13:83288131-114342258)x3 copy number gain See cases [RCV000141804] Chr13:83288131..114342258 [GRCh38]
Chr13:83862266..115107733 [GRCh37]
Chr13:82760267..114125835 [NCBI36]
Chr13:13q31.1-34
pathogenic
GRCh38/hg38 13q31.3-32.1(chr13:93869706-94449189)x3 copy number gain See cases [RCV000142990] Chr13:93869706..94449189 [GRCh38]
Chr13:94521959..95101443 [GRCh37]
Chr13:93319960..93899444 [NCBI36]
Chr13:13q31.3-32.1
uncertain significance
GRCh38/hg38 13q31.3(chr13:93707800-93770810)x1 copy number loss See cases [RCV000142996] Chr13:93707800..93770810 [GRCh38]
Chr13:94360053..94423063 [GRCh37]
Chr13:93158054..93221064 [NCBI36]
Chr13:13q31.3
likely benign
GRCh38/hg38 13q12.11-34(chr13:19671934-114340331)x3 copy number gain See cases [RCV000142924] Chr13:19671934..114340331 [GRCh38]
Chr13:20246074..115085141 [GRCh37]
Chr13:19144074..114123908 [NCBI36]
Chr13:13q12.11-34
pathogenic
GRCh38/hg38 13q11-34(chr13:18862146-114342258)x3 copy number gain See cases [RCV000143462] Chr13:18862146..114342258 [GRCh38]
Chr13:19436286..115107733 [GRCh37]
Chr13:18334286..114125835 [NCBI36]
Chr13:13q11-34
pathogenic
GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3 copy number gain See cases [RCV000148126] Chr13:19837395..114327173 [GRCh38]
Chr13:20411535..115085141 [GRCh37]
Chr13:19309535..114110750 [NCBI36]
Chr13:13q12.11-34
pathogenic
NM_005708.5(GPC6):c.1152+9T>A single nucleotide variant not provided [RCV000179453] Chr13:94306132 [GRCh38]
Chr13:94958386 [GRCh37]
Chr13:13q31.3
conflicting interpretations of pathogenicity|uncertain significance
GRCh37/hg19 13q31.2-34(chr13:89796110-115083342)x1 copy number loss See cases [RCV000240161] Chr13:89796110..115083342 [GRCh37]
Chr13:13q31.2-34
pathogenic
GRCh37/hg19 13q31.3(chr13:91209639-94704856)x3 copy number gain See cases [RCV000240035] Chr13:91209639..94704856 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*135T>C single nucleotide variant Autosomal recessive omodysplasia [RCV000300381] Chr13:94403352 [GRCh38]
Chr13:95055606 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1524G>A (p.Thr508=) single nucleotide variant Autosomal recessive omodysplasia [RCV000345866]|not provided [RCV002056391] Chr13:94403073 [GRCh38]
Chr13:95055327 [GRCh37]
Chr13:13q32.1
likely benign|uncertain significance
NM_005708.5(GPC6):c.991A>T (p.Met331Leu) single nucleotide variant Autosomal recessive omodysplasia [RCV000266598]|not provided [RCV000897478] Chr13:94286462 [GRCh38]
Chr13:94938716 [GRCh37]
Chr13:13q31.3
benign|uncertain significance
NM_005708.5(GPC6):c.*1675C>T single nucleotide variant Autosomal recessive omodysplasia [RCV000285471] Chr13:94404892 [GRCh38]
Chr13:95057146 [GRCh37]
Chr13:13q32.1
benign|uncertain significance
NM_005708.5(GPC6):c.*1665C>A single nucleotide variant Autosomal recessive omodysplasia [RCV000325009]|not provided [RCV004707106] Chr13:94404882 [GRCh38]
Chr13:95057136 [GRCh37]
Chr13:13q32.1
benign
NM_005708.5(GPC6):c.1601G>A (p.Arg534His) single nucleotide variant Autosomal recessive omodysplasia [RCV000306108]|Inborn genetic diseases [RCV003165839]|not provided [RCV001850653] Chr13:94403150 [GRCh38]
Chr13:95055404 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.49C>A (p.Leu17Ile) single nucleotide variant Autosomal recessive omodysplasia [RCV000270002]|Inborn genetic diseases [RCV002522295]|not provided [RCV001850652] Chr13:93227505 [GRCh38]
Chr13:93879758 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*1610A>C single nucleotide variant Autosomal recessive omodysplasia [RCV000272274] Chr13:94404827 [GRCh38]
Chr13:95057081 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1088G>A (p.Arg363His) single nucleotide variant Autosomal recessive omodysplasia [RCV000376855] Chr13:94306059 [GRCh38]
Chr13:94958313 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1234G>A (p.Val412Met) single nucleotide variant Autosomal recessive omodysplasia [RCV000989154]|not provided [RCV001513967] Chr13:94382495 [GRCh38]
Chr13:94382495..94382496 [GRCh38]
Chr13:95034749 [GRCh37]
Chr13:95034749..95034750 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.-69C>T single nucleotide variant Autosomal recessive omodysplasia [RCV000309853] Chr13:93227388 [GRCh38]
Chr13:93879641 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*255G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000355338]|not provided [RCV001636887] Chr13:94403472 [GRCh38]
Chr13:95055726 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.*694CT[1] microsatellite Omodysplasia [RCV000381448] Chr13:94403911..94403912 [GRCh38]
Chr13:95056165..95056166 [GRCh37]
Chr13:13q32.1
likely benign
NM_005708.5(GPC6):c.*1472G>C single nucleotide variant Autosomal recessive omodysplasia [RCV000273863] Chr13:94404689 [GRCh38]
Chr13:95056943 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.-320C>A single nucleotide variant Autosomal recessive omodysplasia [RCV000334792]|not provided [RCV001642970] Chr13:93227137 [GRCh38]
Chr13:93879390 [GRCh37]
Chr13:13q31.3
benign|likely benign
NM_005708.5(GPC6):c.1272C>T (p.Asn424=) single nucleotide variant Autosomal recessive omodysplasia [RCV000294323]|not provided [RCV000900887] Chr13:94382533 [GRCh38]
Chr13:95034787 [GRCh37]
Chr13:13q31.3
benign|likely benign
NM_005708.5(GPC6):c.*4656T>A single nucleotide variant Autosomal recessive omodysplasia [RCV000386197] Chr13:94407873 [GRCh38]
Chr13:95060127 [GRCh37]
Chr13:13q32.1
benign
NM_005708.5(GPC6):c.1129G>A (p.Ala377Thr) single nucleotide variant Autosomal recessive omodysplasia [RCV000263488]|not provided [RCV000321347] Chr13:94306100 [GRCh38]
Chr13:94958354 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*4236G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000315669] Chr13:94407453 [GRCh38]
Chr13:95059707 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1248G>A (p.Thr416=) single nucleotide variant Autosomal recessive omodysplasia [RCV000388270]|not provided [RCV001522921] Chr13:94382509 [GRCh38]
Chr13:95034763 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.*334dup duplication Omodysplasia [RCV000260493] Chr13:94403541..94403542 [GRCh38]
Chr13:95055795..95055796 [GRCh37]
Chr13:13q32.1
benign
NM_005708.5(GPC6):c.*338A>C single nucleotide variant Autosomal recessive omodysplasia [RCV000277816] Chr13:94403555 [GRCh38]
Chr13:95055809 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.*2031A>C single nucleotide variant Autosomal recessive omodysplasia [RCV000281189]|not provided [RCV004707107] Chr13:94405248 [GRCh38]
Chr13:95057502 [GRCh37]
Chr13:13q32.1
benign
NM_005708.5(GPC6):c.1216A>G (p.Ile406Val) single nucleotide variant Autosomal recessive omodysplasia [RCV000278627]|Inborn genetic diseases [RCV004975439] Chr13:94382477 [GRCh38]
Chr13:95034731 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*4182C>A single nucleotide variant Autosomal recessive omodysplasia [RCV000262808]|not provided [RCV004707111] Chr13:94407399 [GRCh38]
Chr13:95059653 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.*2407A>T single nucleotide variant Autosomal recessive omodysplasia [RCV000280032] Chr13:94405624 [GRCh38]
Chr13:95057878 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.*1261G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000300696]|not provided [RCV004705285] Chr13:94404478 [GRCh38]
Chr13:95056732 [GRCh37]
Chr13:13q32.1
likely benign|uncertain significance
NM_005708.5(GPC6):c.*134A>G single nucleotide variant Autosomal recessive omodysplasia [RCV000263992] Chr13:94403351 [GRCh38]
Chr13:95055605 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1026T>G single nucleotide variant Autosomal recessive omodysplasia [RCV000341839] Chr13:94404243 [GRCh38]
Chr13:95056497 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1094T>A single nucleotide variant Autosomal recessive omodysplasia [RCV000391299]|not provided [RCV004707104] Chr13:94404311 [GRCh38]
Chr13:95056565 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.320-6C>G single nucleotide variant not provided [RCV000339637] Chr13:93830148 [GRCh38]
Chr13:94482401 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*3716A>T single nucleotide variant Autosomal recessive omodysplasia [RCV000270775] Chr13:94406933 [GRCh38]
Chr13:95059187 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1033A>G (p.Lys345Glu) single nucleotide variant Autosomal recessive omodysplasia [RCV000322228] Chr13:94306004 [GRCh38]
Chr13:94958258 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*4066A>C single nucleotide variant Autosomal recessive omodysplasia [RCV000322525]|not provided [RCV004708342] Chr13:94407283 [GRCh38]
Chr13:95059537 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.*3723T>G single nucleotide variant Autosomal recessive omodysplasia [RCV000323683]|not provided [RCV004707110] Chr13:94406940 [GRCh38]
Chr13:95059194 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.*3020G>A single nucleotide variant Omodysplasia [RCV000368631] Chr13:94406237 [GRCh38]
Chr13:95058491 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1439T>C single nucleotide variant Autosomal recessive omodysplasia [RCV000370683] Chr13:94404656 [GRCh38]
Chr13:95056910 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1341C>T (p.Pro447=) single nucleotide variant Autosomal recessive omodysplasia [RCV000349287]|not provided [RCV001517555] Chr13:94398517 [GRCh38]
Chr13:95050771 [GRCh37]
Chr13:13q31.3
benign|likely benign|uncertain significance
NM_005708.5(GPC6):c.-133G>T single nucleotide variant Autosomal recessive omodysplasia [RCV000349470] Chr13:93227324 [GRCh38]
Chr13:93879577 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1162A>G (p.Ile388Val) single nucleotide variant Autosomal recessive omodysplasia [RCV000373241]|Inborn genetic diseases [RCV004021576] Chr13:94382423 [GRCh38]
Chr13:95034677 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*4169A>C single nucleotide variant Autosomal recessive omodysplasia [RCV000373791] Chr13:94407386 [GRCh38]
Chr13:95059640 [GRCh37]
Chr13:13q32.1
likely benign|uncertain significance
NM_005708.5(GPC6):c.*333_*334dup duplication Omodysplasia [RCV000315766]|not provided [RCV004693162] Chr13:94403541..94403542 [GRCh38]
Chr13:95055795..95055796 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*672A>G single nucleotide variant Autosomal recessive omodysplasia [RCV000329094] Chr13:94403889 [GRCh38]
Chr13:95056143 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.*2605C>A single nucleotide variant Autosomal recessive omodysplasia [RCV000351183]|not provided [RCV004707108] Chr13:94405822 [GRCh38]
Chr13:95058076 [GRCh37]
Chr13:13q32.1
benign|uncertain significance
NM_005708.5(GPC6):c.-623G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000374269]|not provided [RCV001690035] Chr13:93226834 [GRCh38]
Chr13:93879087 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.*385G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000330464] Chr13:94403602 [GRCh38]
Chr13:95055856 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.*4547G>T single nucleotide variant Autosomal recessive omodysplasia [RCV000352659] Chr13:94407764 [GRCh38]
Chr13:95060018 [GRCh37]
Chr13:13q32.1
benign|uncertain significance
NM_005708.5(GPC6):c.*1983T>G single nucleotide variant Autosomal recessive omodysplasia [RCV000376364] Chr13:94405200 [GRCh38]
Chr13:95057454 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1297C>T single nucleotide variant Autosomal recessive omodysplasia [RCV000402889]|not provided [RCV004707105] Chr13:94404514 [GRCh38]
Chr13:95056768 [GRCh37]
Chr13:13q32.1
benign
NM_005708.5(GPC6):c.1496G>A (p.Ser499Asn) single nucleotide variant Autosomal recessive omodysplasia [RCV000309442]|Inborn genetic diseases [RCV004021577]|not provided [RCV001342728] Chr13:94403045 [GRCh38]
Chr13:95055299 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1297C>G single nucleotide variant Autosomal recessive omodysplasia [RCV000353193] Chr13:94404514 [GRCh38]
Chr13:95056768 [GRCh37]
Chr13:13q32.1
benign|likely benign
NM_005708.5(GPC6):c.-100G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000402433] Chr13:93227357 [GRCh38]
Chr13:93879610 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1570C>T (p.Arg524Trp) single nucleotide variant Autosomal recessive omodysplasia [RCV000403703]|Inborn genetic diseases [RCV002520889]|not provided [RCV001295229] Chr13:94403119 [GRCh38]
Chr13:95055373 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*3693A>G single nucleotide variant Autosomal recessive omodysplasia [RCV000310678]|not provided [RCV004707109] Chr13:94406910 [GRCh38]
Chr13:95059164 [GRCh37]
Chr13:13q32.1
benign
NM_005708.5(GPC6):c.-307T>A single nucleotide variant Autosomal recessive omodysplasia [RCV000404766] Chr13:93227150 [GRCh38]
Chr13:93879403 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*3869A>G single nucleotide variant Autosomal recessive omodysplasia [RCV000265098] Chr13:94407086 [GRCh38]
Chr13:95059340 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.-137C>T single nucleotide variant Autosomal recessive omodysplasia [RCV000313712] Chr13:93227320 [GRCh38]
Chr13:93879573 [GRCh37]
Chr13:13q31.3
benign|uncertain significance
NM_005708.5(GPC6):c.*1419C>T single nucleotide variant Autosomal recessive omodysplasia [RCV000313785] Chr13:94404636 [GRCh38]
Chr13:95056890 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1485A>T (p.Ser495=) single nucleotide variant Autosomal recessive omodysplasia [RCV000408163]|not provided [RCV000902112] Chr13:94403034 [GRCh38]
Chr13:95055288 [GRCh37]
Chr13:13q32.1
benign|uncertain significance
NM_005708.5(GPC6):c.*2240G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000338601] Chr13:94405457 [GRCh38]
Chr13:95057711 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*126G>C single nucleotide variant Autosomal recessive omodysplasia [RCV000360887] Chr13:94403343 [GRCh38]
Chr13:95055597 [GRCh37]
Chr13:13q32.1
likely benign|uncertain significance
NM_005708.5(GPC6):c.585C>T (p.Asp195=) single nucleotide variant Autosomal recessive omodysplasia [RCV000361177] Chr13:93830419 [GRCh38]
Chr13:94482672 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*3833G>C single nucleotide variant Autosomal recessive omodysplasia [RCV000362102]|not provided [RCV004708341] Chr13:94407050 [GRCh38]
Chr13:95059304 [GRCh37]
Chr13:13q32.1
benign
NM_005708.5(GPC6):c.*422A>G single nucleotide variant Autosomal recessive omodysplasia [RCV000387276] Chr13:94403639 [GRCh38]
Chr13:95055893 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1188T>C single nucleotide variant Autosomal recessive omodysplasia [RCV000340539] Chr13:94404405 [GRCh38]
Chr13:95056659 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.-442C>T single nucleotide variant Autosomal recessive omodysplasia [RCV000279772] Chr13:93227015 [GRCh38]
Chr13:93879268 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1137A>C (p.Thr379=) single nucleotide variant Autosomal recessive omodysplasia [RCV000318691] Chr13:94306108 [GRCh38]
Chr13:94958362 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.-23G>T single nucleotide variant Autosomal recessive omodysplasia [RCV000364515] Chr13:93227434 [GRCh38]
Chr13:93879687 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*1474A>G single nucleotide variant Autosomal recessive omodysplasia [RCV000364441] Chr13:94404691 [GRCh38]
Chr13:95056945 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.10T>A (p.Trp4Arg) single nucleotide variant Autosomal recessive omodysplasia [RCV001113912]|GPC6-related disorder [RCV003920044]|not provided [RCV000894368]|not specified [RCV000267947] Chr13:93227466 [GRCh38]
Chr13:93879719 [GRCh37]
Chr13:13q31.3
benign|likely benign
NM_005708.5(GPC6):c.*1473T>C single nucleotide variant Autosomal recessive omodysplasia [RCV000330815] Chr13:94404690 [GRCh38]
Chr13:95056944 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*3701G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000363013] Chr13:94406918 [GRCh38]
Chr13:95059172 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1669T>G single nucleotide variant Omodysplasia [RCV000382007] Chr13:94404886 [GRCh38]
Chr13:95057140 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1169T>C single nucleotide variant Autosomal recessive omodysplasia [RCV000283405] Chr13:94404386 [GRCh38]
Chr13:95056640 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*3439T>C single nucleotide variant Autosomal recessive omodysplasia [RCV000405123] Chr13:94406656 [GRCh38]
Chr13:95058910 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*4476A>G single nucleotide variant Autosomal recessive omodysplasia [RCV000295507] Chr13:94407693 [GRCh38]
Chr13:95059947 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.161-4G>T single nucleotide variant Autosomal recessive omodysplasia [RCV000306438] Chr13:93545259 [GRCh38]
Chr13:94197512 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*1225C>G single nucleotide variant Autosomal recessive omodysplasia [RCV000405823] Chr13:94404442 [GRCh38]
Chr13:95056696 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*334del deletion Omodysplasia [RCV000389016] Chr13:94403542 [GRCh38]
Chr13:95055796 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1800T>G single nucleotide variant Autosomal recessive omodysplasia [RCV000324105] Chr13:94405017 [GRCh38]
Chr13:95057271 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*4239A>G single nucleotide variant Autosomal recessive omodysplasia [RCV000372684] Chr13:94407456 [GRCh38]
Chr13:95059710 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2799G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000391714] Chr13:94406016 [GRCh38]
Chr13:95058270 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2299A>G single nucleotide variant Autosomal recessive omodysplasia [RCV000391722] Chr13:94405516 [GRCh38]
Chr13:95057770 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2852C>G single nucleotide variant Autosomal recessive omodysplasia [RCV000311565] Chr13:94406069 [GRCh38]
Chr13:95058323 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*854A>T single nucleotide variant Omodysplasia [RCV000289242] Chr13:94404071 [GRCh38]
Chr13:95056325 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*522G>A single nucleotide variant Autosomal recessive omodysplasia [RCV000290660] Chr13:94403739 [GRCh38]
Chr13:95055993 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.256C>T (p.Leu86Phe) single nucleotide variant Autosomal recessive omodysplasia [RCV001113915]|not provided [RCV000954976]|not specified [RCV000731241] Chr13:93545358 [GRCh38]
Chr13:94197611 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.930G>A (p.Ser310=) single nucleotide variant not provided [RCV000733955] Chr13:94286401 [GRCh38]
Chr13:94938655 [GRCh37]
Chr13:13q31.3
conflicting interpretations of pathogenicity|uncertain significance
GRCh37/hg19 13q14.3-33.3(chr13:53551300-109850651)x1 copy number loss See cases [RCV000449272] Chr13:53551300..109850651 [GRCh37]
Chr13:13q14.3-33.3
pathogenic
GRCh37/hg19 13q21.2-34(chr13:61424168-115107733)x3 copy number gain See cases [RCV000449118] Chr13:61424168..115107733 [GRCh37]
Chr13:13q21.2-34
pathogenic
GRCh37/hg19 13q12.11-34(chr13:19571503-115092510) copy number gain See cases [RCV000449142] Chr13:19571503..115092510 [GRCh37]
Chr13:13q12.11-34
pathogenic
GRCh37/hg19 13q31.3-34(chr13:94269729-115107733)x3 copy number gain See cases [RCV000447545] Chr13:94269729..115107733 [GRCh37]
Chr13:13q31.3-34
pathogenic
GRCh37/hg19 13q31.1-34(chr13:82221361-115092569)x3 copy number gain See cases [RCV000447429] Chr13:82221361..115092569 [GRCh37]
Chr13:13q31.1-34
pathogenic
GRCh37/hg19 13q21.1-34(chr13:56431743-115107733) copy number gain See cases [RCV000510722] Chr13:56431743..115107733 [GRCh37]
Chr13:13q21.1-34
pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3 copy number gain See cases [RCV000445886] Chr13:19436286..115107733 [GRCh37]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q31.3(chr13:93103385-94100309)x3 copy number gain See cases [RCV000445914] Chr13:93103385..94100309 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q31.1-33.1(chr13:81851091-102864674)x1 copy number loss See cases [RCV000448988] Chr13:81851091..102864674 [GRCh37]
Chr13:13q31.1-33.1
pathogenic
GRCh37/hg19 13q31.2-34(chr13:88073140-115107733)x1 copy number loss See cases [RCV000448405] Chr13:88073140..115107733 [GRCh37]
Chr13:13q31.2-34
pathogenic
GRCh37/hg19 13q31.3(chr13:94069660-94324629)x1 copy number loss See cases [RCV000510507] Chr13:94069660..94324629 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q31.3-34(chr13:94474530-115107733)x1 copy number loss See cases [RCV000510535] Chr13:94474530..115107733 [GRCh37]
Chr13:13q31.3-34
pathogenic
GRCh37/hg19 13q21.33-34(chr13:71871468-115107733)x4 copy number gain See cases [RCV000510281] Chr13:71871468..115107733 [GRCh37]
Chr13:13q21.33-34
pathogenic
GRCh37/hg19 13q31.1-34(chr13:80058840-115107733)x3 copy number gain See cases [RCV000510566] Chr13:80058840..115107733 [GRCh37]
Chr13:13q31.1-34
pathogenic
GRCh37/hg19 13q31.3-32.1(chr13:94521536-95111513)x3 copy number gain See cases [RCV000511830] Chr13:94521536..95111513 [GRCh37]
Chr13:13q31.3-32.1
uncertain significance
GRCh37/hg19 13q11-34(chr13:19436287-115107733)x3 copy number gain See cases [RCV000511880] Chr13:19436287..115107733 [GRCh37]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q31.3-32.1(chr13:94522837-95111524)x3 copy number gain See cases [RCV000511062] Chr13:94522837..95111524 [GRCh37]
Chr13:13q31.3-32.1
uncertain significance
GRCh37/hg19 13q31.1-33.3(chr13:80572498-108719528)x1 copy number loss See cases [RCV000510890] Chr13:80572498..108719528 [GRCh37]
Chr13:13q31.1-33.3
pathogenic
GRCh37/hg19 13q31.1-34(chr13:83435292-115107733)x3 copy number gain See cases [RCV000512605] Chr13:83435292..115107733 [GRCh37]
Chr13:13q31.1-34
pathogenic
GRCh37/hg19 13q14.3-32.1(chr13:53932358-96586363)x3 copy number gain See cases [RCV000512571] Chr13:53932358..96586363 [GRCh37]
Chr13:13q14.3-32.1
pathogenic
GRCh37/hg19 13q31.1-34(chr13:85176519-115107733)x3 copy number gain See cases [RCV000512242] Chr13:85176519..115107733 [GRCh37]
Chr13:13q31.1-34
pathogenic
Single allele duplication not provided [RCV000678035] Chr13:91209639..94704856 [GRCh37]
Chr13:13q31.3
likely pathogenic
Single allele duplication not provided [RCV000677953] Chr13:93281466..94095389 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q31.3-33.3(chr13:94703767-109731879)x1 copy number loss not provided [RCV000683570] Chr13:94703767..109731879 [GRCh37]
Chr13:13q31.3-33.3
pathogenic
GRCh37/hg19 13q31.3(chr13:94925496-94988058)x1 copy number loss not provided [RCV000683483] Chr13:94925496..94988058 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q31.3(chr13:94034139-94204243)x1 copy number loss not provided [RCV000683496] Chr13:94034139..94204243 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q31.3-32.1(chr13:94857382-96639428)x3 copy number gain not provided [RCV000683550] Chr13:94857382..96639428 [GRCh37]
Chr13:13q31.3-32.1
uncertain significance
GRCh37/hg19 13q31.3-32.1(chr13:93348248-96975820)x3 copy number gain not provided [RCV000683560] Chr13:93348248..96975820 [GRCh37]
Chr13:13q31.3-32.1
uncertain significance
GRCh37/hg19 13q22.3-34(chr13:78590089-115107733)x3 copy number gain not provided [RCV000683571] Chr13:78590089..115107733 [GRCh37]
Chr13:13q22.3-34
pathogenic
GRCh37/hg19 13q31.3(chr13:92072601-94181118)x3 copy number gain not provided [RCV000683553] Chr13:92072601..94181118 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q11-34(chr13:19058717-115103529)x3 copy number gain not provided [RCV000738115] Chr13:19058717..115103529 [GRCh37]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q31.3(chr13:93935502-93947476)x1 copy number loss not provided [RCV000738327] Chr13:93935502..93947476 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94167648-94174180)x3 copy number gain not provided [RCV000738328] Chr13:94167648..94174180 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94167933-94174671)x3 copy number gain not provided [RCV000738329] Chr13:94167933..94174671 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94193124-94196853)x1 copy number loss not provided [RCV000738330] Chr13:94193124..94196853 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94194866-94195192)x3 copy number gain not provided [RCV000738331] Chr13:94194866..94195192 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94233129-94729994)x1 copy number loss not provided [RCV000738332] Chr13:94233129..94729994 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94243975-94247411)x3 copy number gain not provided [RCV000738333] Chr13:94243975..94247411 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94393854-94453765)x1 copy number loss not provided [RCV000738334] Chr13:94393854..94453765 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94456159-94467985)x1 copy number loss not provided [RCV000738335] Chr13:94456159..94467985 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94515699-94543161)x1 copy number loss not provided [RCV000738336] Chr13:94515699..94543161 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94565251-94732738)x1 copy number loss not provided [RCV000738337] Chr13:94565251..94732738 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q21.1-31.3(chr13:57058434-94684615)x1 copy number loss not provided [RCV000750731] Chr13:57058434..94684615 [GRCh37]
Chr13:13q21.1-31.3
pathogenic
GRCh37/hg19 13q31.3(chr13:94641368-94646941)x1 copy number loss not provided [RCV000750854] Chr13:94641368..94646941 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3(chr13:94686454-94703305)x1 copy number loss not provided [RCV000750855] Chr13:94686454..94703305 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3-32.1(chr13:94794736-95024454)x3 copy number gain not provided [RCV000750856] Chr13:94794736..95024454 [GRCh37]
Chr13:13q31.3-32.1
benign
NM_005708.5(GPC6):c.510A>G (p.Glu170=) single nucleotide variant not provided [RCV000915726] Chr13:93830344 [GRCh38]
Chr13:94482597 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1008+52A>G single nucleotide variant not provided [RCV001609857] Chr13:94286531 [GRCh38]
Chr13:94938785 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.161-300G>A single nucleotide variant not provided [RCV001709436] Chr13:93544963 [GRCh38]
Chr13:94197216 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.711+93dup duplication not provided [RCV001692677] Chr13:93830612..93830613 [GRCh38]
Chr13:94482865..94482866 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1289+106G>T single nucleotide variant not provided [RCV001708907] Chr13:94382656 [GRCh38]
Chr13:95034910 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1289+233T>A single nucleotide variant not provided [RCV001678720] Chr13:94382783 [GRCh38]
Chr13:95035037 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.141C>T (p.Ile47=) single nucleotide variant Autosomal recessive omodysplasia [RCV001113914] Chr13:93227597 [GRCh38]
Chr13:93879850 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.576A>G (p.Lys192=) single nucleotide variant not provided [RCV000904966] Chr13:93830410 [GRCh38]
Chr13:94482663 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.712-5T>C single nucleotide variant not provided [RCV000973731] Chr13:94027724 [GRCh38]
Chr13:94679978 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.78G>A (p.Lys26=) single nucleotide variant not provided [RCV000925513] Chr13:93227534 [GRCh38]
Chr13:93879787 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.93A>G (p.Gly31=) single nucleotide variant not provided [RCV000979153] Chr13:93227549 [GRCh38]
Chr13:93879802 [GRCh37]
Chr13:13q31.3
likely benign
GRCh37/hg19 13q14.3-34(chr13:53262013-115107733)x1 copy number loss not provided [RCV001006567] Chr13:53262013..115107733 [GRCh37]
Chr13:13q14.3-34
pathogenic
NM_005708.5(GPC6):c.*1897G>C single nucleotide variant Autosomal recessive omodysplasia [RCV001114106] Chr13:94405114 [GRCh38]
Chr13:95057368 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1693C>A single nucleotide variant Autosomal recessive omodysplasia [RCV001114104] Chr13:94404910 [GRCh38]
Chr13:95057164 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*271T>A single nucleotide variant Autosomal recessive omodysplasia [RCV001114016]|not provided [RCV004707547] Chr13:94403488 [GRCh38]
Chr13:95055742 [GRCh37]
Chr13:13q32.1
benign
GRCh37/hg19 13q21.2-34(chr13:61775567-115107733)x3 copy number gain not provided [RCV000848025] Chr13:61775567..115107733 [GRCh37]
Chr13:13q21.2-34
pathogenic
GRCh37/hg19 13q31.3-34(chr13:94849303-115107733)x3 copy number gain not provided [RCV000847710] Chr13:94849303..115107733 [GRCh37]
Chr13:13q31.3-34
uncertain significance
NM_005708.5(GPC6):c.-248G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001112572] Chr13:93227209 [GRCh38]
Chr13:93879462 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.-113G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001112573] Chr13:93227344 [GRCh38]
Chr13:93879597 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*1528G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001112754] Chr13:94404745 [GRCh38]
Chr13:95056999 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*3497G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001112827] Chr13:94406714 [GRCh38]
Chr13:95058968 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*3639G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001112830] Chr13:94406856 [GRCh38]
Chr13:95059110 [GRCh37]
Chr13:13q32.1
uncertain significance
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3 copy number gain not provided [RCV000849129] Chr13:19436286..115107733 [GRCh37]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q31.3(chr13:94097218-94204671)x1 copy number loss not provided [RCV000845797] Chr13:94097218..94204671 [GRCh37]
Chr13:13q31.3
pathogenic
NM_005708.5(GPC6):c.1289+13C>T single nucleotide variant Autosomal recessive omodysplasia [RCV001110677] Chr13:94382563 [GRCh38]
Chr13:95034817 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1436A>G (p.Asn479Ser) single nucleotide variant Autosomal recessive omodysplasia [RCV001110678] Chr13:94398612 [GRCh38]
Chr13:95050866 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*3031G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001110841] Chr13:94406248 [GRCh38]
Chr13:95058502 [GRCh37]
Chr13:13q32.1
uncertain significance
GRCh37/hg19 13q31.3(chr13:94627872-94683687)x1 copy number loss not provided [RCV001006587] Chr13:94627872..94683687 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*1035C>T single nucleotide variant Autosomal recessive omodysplasia [RCV001109979] Chr13:94404252 [GRCh38]
Chr13:95056506 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2212T>C single nucleotide variant Autosomal recessive omodysplasia [RCV001110068] Chr13:94405429 [GRCh38]
Chr13:95057683 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2305C>T single nucleotide variant Autosomal recessive omodysplasia [RCV001110070] Chr13:94405522 [GRCh38]
Chr13:95057776 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2455C>T single nucleotide variant Autosomal recessive omodysplasia [RCV001110071] Chr13:94405672 [GRCh38]
Chr13:95057926 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1255G>A (p.Glu419Lys) single nucleotide variant not provided [RCV003106544] Chr13:94382516 [GRCh38]
Chr13:95034770 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1153-128T>C single nucleotide variant not provided [RCV001652908] Chr13:94382286 [GRCh38]
Chr13:95034540 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.711+86A>C single nucleotide variant not provided [RCV001713810] Chr13:93830631 [GRCh38]
Chr13:94482884 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1289+113G>A single nucleotide variant not provided [RCV001638342] Chr13:94382663 [GRCh38]
Chr13:95034917 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.319+86545G>T single nucleotide variant not provided [RCV001638378] Chr13:93631966 [GRCh38]
Chr13:94284219 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.319+86315C>G single nucleotide variant not provided [RCV001656025] Chr13:93631736 [GRCh38]
Chr13:94283989 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1009-134T>A single nucleotide variant not provided [RCV001639918] Chr13:94305846 [GRCh38]
Chr13:94958100 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1153-313C>G single nucleotide variant not provided [RCV001541169] Chr13:94382101 [GRCh38]
Chr13:95034355 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.64G>A (p.Gly22Arg) single nucleotide variant Autosomal recessive omodysplasia [RCV001113913]|not provided [RCV000888774] Chr13:93227520 [GRCh38]
Chr13:93879773 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1338T>C (p.Asn446=) single nucleotide variant not provided [RCV000910073] Chr13:94398514 [GRCh38]
Chr13:95050768 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.984A>G (p.Glu328=) single nucleotide variant not provided [RCV000925992] Chr13:94286455 [GRCh38]
Chr13:94938709 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.195A>G (p.Thr65=) single nucleotide variant not provided [RCV000916605] Chr13:93545297 [GRCh38]
Chr13:94197550 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.189A>G (p.Glu63=) single nucleotide variant GPC6-related disorder [RCV003975670]|not provided [RCV000895516] Chr13:93545291 [GRCh38]
Chr13:94197544 [GRCh37]
Chr13:13q31.3
benign|likely benign
NM_005708.5(GPC6):c.284G>A (p.Arg95His) single nucleotide variant Autosomal recessive omodysplasia [RCV001113916]|GPC6-related disorder [RCV004731092] Chr13:93545386 [GRCh38]
Chr13:94197639 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*38A>T single nucleotide variant Autosomal recessive omodysplasia [RCV001114014] Chr13:94403255 [GRCh38]
Chr13:95055509 [GRCh37]
Chr13:13q32.1
likely benign
NM_005708.5(GPC6):c.1512C>T (p.Asp504=) single nucleotide variant Autosomal recessive omodysplasia [RCV001112655]|not provided [RCV002069815] Chr13:94403061 [GRCh38]
Chr13:95055315 [GRCh37]
Chr13:13q32.1
likely benign|uncertain significance
NM_005708.5(GPC6):c.1566C>T (p.Pro522=) single nucleotide variant Autosomal recessive omodysplasia [RCV001112656] Chr13:94403115 [GRCh38]
Chr13:95055369 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*3623G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001112829] Chr13:94406840 [GRCh38]
Chr13:95059094 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1228G>A (p.Glu410Lys) single nucleotide variant Autosomal recessive omodysplasia [RCV002470462] Chr13:94382489 [GRCh38]
Chr13:95034743 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.711+92_711+93dup duplication not provided [RCV001595314] Chr13:93830612..93830613 [GRCh38]
Chr13:94482865..94482866 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.711+92_711+93del deletion not provided [RCV001720674] Chr13:93830613..93830614 [GRCh38]
Chr13:94482866..94482867 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.711+93del deletion not provided [RCV001639346] Chr13:93830613 [GRCh38]
Chr13:94482866 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1289+327A>T single nucleotide variant not provided [RCV001657547] Chr13:94382877 [GRCh38]
Chr13:95035131 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.711+7G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001109891] Chr13:93830552 [GRCh38]
Chr13:94482805 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*1032C>T single nucleotide variant Autosomal recessive omodysplasia [RCV001109978] Chr13:94404249 [GRCh38]
Chr13:95056503 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2269G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001110069] Chr13:94405486 [GRCh38]
Chr13:95057740 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*3234A>G single nucleotide variant Autosomal recessive omodysplasia [RCV001112825] Chr13:94406451 [GRCh38]
Chr13:95058705 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1037C>T (p.Pro346Leu) single nucleotide variant Autosomal recessive omodysplasia [RCV001109892] Chr13:94306008 [GRCh38]
Chr13:94958262 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*734C>A single nucleotide variant Autosomal recessive omodysplasia [RCV001109977] Chr13:94403951 [GRCh38]
Chr13:95056205 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2465A>G single nucleotide variant Autosomal recessive omodysplasia [RCV001110072] Chr13:94405682 [GRCh38]
Chr13:95057936 [GRCh37]
Chr13:13q32.1
benign
NM_005708.5(GPC6):c.*4424T>G single nucleotide variant Autosomal recessive omodysplasia [RCV001110151] Chr13:94407641 [GRCh38]
Chr13:95059895 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.-478C>G single nucleotide variant Autosomal recessive omodysplasia [RCV001110588] Chr13:93226979 [GRCh38]
Chr13:93879232 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.*1375C>T single nucleotide variant Autosomal recessive omodysplasia [RCV001110765] Chr13:94404592 [GRCh38]
Chr13:95056846 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2582C>G single nucleotide variant Autosomal recessive omodysplasia [RCV001110838] Chr13:94405799 [GRCh38]
Chr13:95058053 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2646T>G single nucleotide variant Autosomal recessive omodysplasia [RCV001110839] Chr13:94405863 [GRCh38]
Chr13:95058117 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*2791G>T single nucleotide variant Autosomal recessive omodysplasia [RCV001110840] Chr13:94406008 [GRCh38]
Chr13:95058262 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*3118A>G single nucleotide variant Autosomal recessive omodysplasia [RCV001110842] Chr13:94406335 [GRCh38]
Chr13:95058589 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.319+86317G>A single nucleotide variant not provided [RCV001694306] Chr13:93631738 [GRCh38]
Chr13:94283991 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1466-133A>C single nucleotide variant not provided [RCV001616695] Chr13:94402882 [GRCh38]
Chr13:95055136 [GRCh37]
Chr13:13q32.1
benign
NM_005708.5(GPC6):c.319+111352A>G single nucleotide variant not provided [RCV001680377] Chr13:93656773 [GRCh38]
Chr13:94309026 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.710A>G (p.Lys237Arg) single nucleotide variant not provided [RCV001572983] Chr13:93830544 [GRCh38]
Chr13:94482797 [GRCh37]
Chr13:13q31.3
likely benign|uncertain significance
NC_000013.11:g.93226778A>G single nucleotide variant not provided [RCV001668764] Chr13:93226778 [GRCh38]
Chr13:93879031 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.320-183A>G single nucleotide variant not provided [RCV001679463] Chr13:93829971 [GRCh38]
Chr13:94482224 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13q31.3-32.1(chr13:94896219-96993668)x3 copy number gain not provided [RCV001006588] Chr13:94896219..96993668 [GRCh37]
Chr13:13q31.3-32.1
uncertain significance
NM_005708.5(GPC6):c.*3308G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001112826] Chr13:94406525 [GRCh38]
Chr13:95058779 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*3571T>C single nucleotide variant Autosomal recessive omodysplasia [RCV001112828] Chr13:94406788 [GRCh38]
Chr13:95059042 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*254C>T single nucleotide variant Autosomal recessive omodysplasia [RCV001114015] Chr13:94403471 [GRCh38]
Chr13:95055725 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1792G>A single nucleotide variant Autosomal recessive omodysplasia [RCV001114105] Chr13:94405009 [GRCh38]
Chr13:95057263 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1567G>A (p.Asp523Asn) single nucleotide variant Inborn genetic diseases [RCV004031129]|not provided [RCV001040143] Chr13:94403116 [GRCh38]
Chr13:95055370 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*22A>G single nucleotide variant Autosomal recessive omodysplasia [RCV001112657] Chr13:94403239 [GRCh38]
Chr13:95055493 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.*1457C>G single nucleotide variant Autosomal recessive omodysplasia [RCV001112753] Chr13:94404674 [GRCh38]
Chr13:95056928 [GRCh37]
Chr13:13q32.1
uncertain significance
GRCh37/hg19 13q31.3(chr13:94754706-94888187)x1 copy number loss not provided [RCV001259164] Chr13:94754706..94888187 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.578A>T (p.Tyr193Phe) single nucleotide variant Inborn genetic diseases [RCV004042154]|not provided [RCV001964448] Chr13:93830412 [GRCh38]
Chr13:94482665 [GRCh37]
Chr13:13q31.3
uncertain significance
NC_000013.10:g.(?_94938593)_(95102698_?)dup duplication not provided [RCV001374140] Chr13:94938593..95102698 [GRCh37]
Chr13:13q31.3-32.1
uncertain significance
GRCh37/hg19 13q11-34(chr13:19053605-115108528)x3 copy number gain See cases [RCV001353184] Chr13:19053605..115108528 [GRCh37]
Chr13:13q11-34
pathogenic
Single allele deletion Distal monosomy 13q [RCV001391677] Chr13:94679977..111536145 [GRCh37]
Chr13:13q31.3-34
pathogenic
NM_005708.5(GPC6):c.1424A>G (p.Lys475Arg) single nucleotide variant not provided [RCV001325623] Chr13:94398600 [GRCh38]
Chr13:95050854 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.14_15inv (p.Ile5Arg) inversion not provided [RCV001326341] Chr13:93227470..93227471 [GRCh38]
Chr13:93879723..93879724 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.452C>A (p.Thr151Asn) single nucleotide variant not provided [RCV001321381] Chr13:93830286 [GRCh38]
Chr13:94482539 [GRCh37]
Chr13:13q31.3
uncertain significance
NC_000013.10:g.(?_92002837)_(103343314_?)del deletion Holoprosencephaly 5 [RCV001388033] Chr13:92002837..103343314 [GRCh37]
Chr13:13q31.3-33.1
pathogenic
NC_000013.10:g.(?_94482407)_(94482798_?)del deletion not provided [RCV001384896] Chr13:94482407..94482798 [GRCh37]
Chr13:13q31.3
pathogenic
NM_005708.5(GPC6):c.132G>C (p.Leu44=) single nucleotide variant not provided [RCV001400410] Chr13:93227588 [GRCh38]
Chr13:93879841 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.433_451del (p.Glu145fs) deletion not provided [RCV001389748] Chr13:93830264..93830282 [GRCh38]
Chr13:94482517..94482535 [GRCh37]
Chr13:13q31.3
pathogenic
NM_005708.5(GPC6):c.942G>A (p.Pro314=) single nucleotide variant not provided [RCV001439723] Chr13:94286413 [GRCh38]
Chr13:94938667 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.319+86342A>G single nucleotide variant not provided [RCV001645132] Chr13:93631763 [GRCh38]
Chr13:94284016 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.909G>A (p.Glu303=) single nucleotide variant not provided [RCV001486007] Chr13:94286380 [GRCh38]
Chr13:94938634 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.319+61454A>G single nucleotide variant not provided [RCV001643481] Chr13:93606875 [GRCh38]
Chr13:94259128 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1290-232A>G single nucleotide variant not provided [RCV001684657] Chr13:94398234 [GRCh38]
Chr13:95050488 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.877+144A>T single nucleotide variant not provided [RCV001654835] Chr13:94028038 [GRCh38]
Chr13:94680292 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.711+226T>C single nucleotide variant not provided [RCV001687428] Chr13:93830771 [GRCh38]
Chr13:94483024 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.474G>A (p.Glu158=) single nucleotide variant not provided [RCV001398589] Chr13:93830308 [GRCh38]
Chr13:94482561 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.319+177del deletion not provided [RCV001538777] Chr13:93545586 [GRCh38]
Chr13:94197839 [GRCh37]
Chr13:13q31.3
benign
GRCh37/hg19 13p13-q34(chr13:1-115169878)x3 copy number gain See cases [RCV001780076] Chr13:1..115169878 [GRCh37]
Chr13:13p13-q34
pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-115107733) copy number gain not specified [RCV002053036] Chr13:19436286..115107733 [GRCh37]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q22.3-34(chr13:78514567-115107733) copy number gain not specified [RCV002053071] Chr13:78514567..115107733 [GRCh37]
Chr13:13q22.3-34
pathogenic
GRCh37/hg19 13q31.1-34(chr13:85037147-115107733) copy number gain not specified [RCV002053073] Chr13:85037147..115107733 [GRCh37]
Chr13:13q31.1-34
pathogenic
NM_005708.5(GPC6):c.1619C>T (p.Ser540Phe) single nucleotide variant not provided [RCV001926574] Chr13:94403168 [GRCh38]
Chr13:95055422 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.485A>G (p.Asn162Ser) single nucleotide variant Autosomal recessive omodysplasia [RCV003453909]|Inborn genetic diseases [RCV004631886]|not provided [RCV002005424] Chr13:93830319 [GRCh38]
Chr13:94482572 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q21.2-34(chr13:61424168-115107733) copy number gain not specified [RCV002053063] Chr13:61424168..115107733 [GRCh37]
Chr13:13q21.2-34
pathogenic
NM_005708.5(GPC6):c.613C>T (p.Arg205Trp) single nucleotide variant not provided [RCV001966925] Chr13:93830447 [GRCh38]
Chr13:94482700 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1435A>G (p.Asn479Asp) single nucleotide variant Inborn genetic diseases [RCV002551145]|not provided [RCV001872881] Chr13:94398611 [GRCh38]
Chr13:95050865 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3 copy number gain not provided [RCV001834436] Chr13:19436286..115107733 [GRCh37]
Chr13:13q11-34
pathogenic
NM_005708.5(GPC6):c.376C>T (p.Arg126Trp) single nucleotide variant not provided [RCV001947232] Chr13:93830210 [GRCh38]
Chr13:94482463 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.83G>C (p.Arg28Pro) single nucleotide variant not provided [RCV001985420] Chr13:93227539 [GRCh38]
Chr13:93879792 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q11-34(chr13:19436286-114981726) copy number gain not specified [RCV002053035] Chr13:19436286..114981726 [GRCh37]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q31.1-34(chr13:79370012-115107733) copy number loss not specified [RCV002053072] Chr13:79370012..115107733 [GRCh37]
Chr13:13q31.1-34
pathogenic
GRCh37/hg19 13q14.11-33.3(chr13:42504540-108206269)x3 copy number gain not provided [RCV001829235] Chr13:42504540..108206269 [GRCh37]
Chr13:13q14.11-33.3
pathogenic
NM_005708.5(GPC6):c.1254C>A (p.Asn418Lys) single nucleotide variant not provided [RCV001891248] Chr13:94382515 [GRCh38]
Chr13:95034769 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q31.2-34(chr13:88073140-115107733) copy number loss not specified [RCV002053074] Chr13:88073140..115107733 [GRCh37]
Chr13:13q31.2-34
pathogenic
NM_005708.5(GPC6):c.512G>A (p.Arg171Gln) single nucleotide variant not provided [RCV002021237] Chr13:93830346 [GRCh38]
Chr13:94482599 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1663A>G (p.Arg555Gly) single nucleotide variant Inborn genetic diseases [RCV002579538]|not provided [RCV002000370] Chr13:94403212 [GRCh38]
Chr13:95055466 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.511C>T (p.Arg171Trp) single nucleotide variant not provided [RCV001880415] Chr13:93830345 [GRCh38]
Chr13:94482598 [GRCh37]
Chr13:13q31.3
pathogenic
NM_005708.5(GPC6):c.1523C>T (p.Thr508Met) single nucleotide variant not provided [RCV002050585] Chr13:94403072 [GRCh38]
Chr13:95055326 [GRCh37]
Chr13:13q32.1
uncertain significance
NC_000013.10:g.(?_95034648)_(96443284_?)dup duplication not provided [RCV001920618] Chr13:95034648..96443284 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1148G>A (p.Arg383Gln) single nucleotide variant Inborn genetic diseases [RCV002571324]|not provided [RCV001975809] Chr13:94306119 [GRCh38]
Chr13:94958373 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.319G>A (p.Glu107Lys) single nucleotide variant not provided [RCV001903530] Chr13:93545421 [GRCh38]
Chr13:94197674 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1121C>A (p.Thr374Lys) single nucleotide variant not provided [RCV001916518] Chr13:94306092 [GRCh38]
Chr13:94958346 [GRCh37]
Chr13:13q31.3
uncertain significance
NC_000013.10:g.(?_93879710)_(93879889_?)dup duplication not provided [RCV001997255] Chr13:93879710..93879889 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.453T>G (p.Thr151=) single nucleotide variant not provided [RCV001960569] Chr13:93830287 [GRCh38]
Chr13:94482540 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1555G>A (p.Ala519Thr) single nucleotide variant Inborn genetic diseases [RCV003264295]|not provided [RCV001982153] Chr13:94403104 [GRCh38]
Chr13:95055358 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.867T>G (p.Asn289Lys) single nucleotide variant Inborn genetic diseases [RCV004975979]|not provided [RCV001979841] Chr13:94027884 [GRCh38]
Chr13:94680138 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.203C>G (p.Thr68Ser) single nucleotide variant not provided [RCV001926184] Chr13:93545305 [GRCh38]
Chr13:94197558 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.548G>T (p.Ser183Ile) single nucleotide variant not provided [RCV001957549] Chr13:93830382 [GRCh38]
Chr13:94482635 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1464A>G (p.Thr488=) single nucleotide variant not provided [RCV001940219] Chr13:94398640 [GRCh38]
Chr13:95050894 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.853G>A (p.Asp285Asn) single nucleotide variant not provided [RCV001937206] Chr13:94027870 [GRCh38]
Chr13:94680124 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1631C>G (p.Thr544Ser) single nucleotide variant not provided [RCV001903490] Chr13:94403180 [GRCh38]
Chr13:95055434 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.712-11T>C single nucleotide variant not provided [RCV002110114] Chr13:94027718 [GRCh38]
Chr13:94679972 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.192T>C (p.Tyr64=) single nucleotide variant GPC6-related disorder [RCV003941264]|not provided [RCV002087189] Chr13:93545294 [GRCh38]
Chr13:94197547 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.712-16T>C single nucleotide variant not provided [RCV002146418] Chr13:94027713 [GRCh38]
Chr13:94679967 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1289+14G>A single nucleotide variant not provided [RCV002208880] Chr13:94382564 [GRCh38]
Chr13:95034818 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1289+15A>G single nucleotide variant not provided [RCV002127319] Chr13:94382565 [GRCh38]
Chr13:95034819 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.1428C>T (p.Asn476=) single nucleotide variant not provided [RCV002167369] Chr13:94398604 [GRCh38]
Chr13:95050858 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.43C>T (p.Leu15=) single nucleotide variant not provided [RCV002125740] Chr13:93227499 [GRCh38]
Chr13:93879752 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.160+11G>A single nucleotide variant not provided [RCV002134563] Chr13:93227627 [GRCh38]
Chr13:93879880 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1554C>T (p.Pro518=) single nucleotide variant not provided [RCV002206633] Chr13:94403103 [GRCh38]
Chr13:95055357 [GRCh37]
Chr13:13q32.1
likely benign
NM_005708.5(GPC6):c.1465+11C>A single nucleotide variant not provided [RCV002159672] Chr13:94398652 [GRCh38]
Chr13:95050906 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.878-12G>C single nucleotide variant not provided [RCV002138265] Chr13:94286337 [GRCh38]
Chr13:94938591 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.96G>C (p.Glu32Asp) single nucleotide variant Inborn genetic diseases [RCV003006975]|not provided [RCV002217561] Chr13:93227552 [GRCh38]
Chr13:93879805 [GRCh37]
Chr13:13q31.3
benign|uncertain significance
NC_000013.10:g.(?_93879710)_(95248390_?)del deletion not provided [RCV003116416] Chr13:93879710..95248390 [GRCh37]
Chr13:13q31.3-32.1
pathogenic
NC_000013.10:g.(?_93879710)_(94482818_?)del deletion not provided [RCV003116417] Chr13:93879710..94482818 [GRCh37]
Chr13:13q31.3
pathogenic
NC_000013.10:g.(?_93879710)_(96443284_?)dup duplication not provided [RCV003116418] Chr13:93879710..96443284 [GRCh37]
Chr13:13q31.3-32.1
uncertain significance
GRCh37/hg19 13q31.2-34(chr13:89490345-115062235)x3 copy number gain See cases [RCV002286354] Chr13:89490345..115062235 [GRCh37]
Chr13:13q31.2-34
pathogenic
GRCh37/hg19 13p13-q34(chr13:1-115169878) copy number gain Complete trisomy 13 syndrome [RCV002280659] Chr13:1..115169878 [GRCh37]
Chr13:13p13-q34
pathogenic
GRCh37/hg19 13q11-34(chr13:19253848-115108937)x3 copy number gain not provided [RCV002291540] Chr13:19253848..115108937 [GRCh37]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q31.3-32.1(chr13:94738479-95001858)x3 copy number gain not provided [RCV002473901] Chr13:94738479..95001858 [GRCh37]
Chr13:13q31.3-32.1
uncertain significance
GRCh37/hg19 13q31.3(chr13:92072602-94178694)x3 copy number gain not provided [RCV002474659] Chr13:92072602..94178694 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh37/hg19 13q31.3-33.2(chr13:93535335-105788229)x1 copy number loss not provided [RCV002473593] Chr13:93535335..105788229 [GRCh37]
Chr13:13q31.3-33.2
pathogenic
GRCh37/hg19 13q22.1-34(chr13:75268539-115107733)x3 copy number gain not provided [RCV002472537] Chr13:75268539..115107733 [GRCh37]
Chr13:13q22.1-34
pathogenic
NM_005708.5(GPC6):c.1228G>C (p.Glu410Gln) single nucleotide variant Inborn genetic diseases [RCV002946591] Chr13:94382489 [GRCh38]
Chr13:95034743 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.877+15_877+16insTGTGATTCTTAAACACCTTCATCATGGAACTCTCAGAGTGGGGTCCGTTTTGGTTTCCTGGTGGTGGGTTTTNNNNNNNNNNAAAAAAAAAAAAAAAAAAAAAAGAAGTGTTTAA microsatellite not provided [RCV002862129] Chr13:94027896..94027897 [GRCh38]
Chr13:94680150..94680151 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1613T>G (p.Leu538Arg) single nucleotide variant not provided [RCV002618064] Chr13:94403162 [GRCh38]
Chr13:95055416 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.923T>A (p.Ile308Asn) single nucleotide variant Inborn genetic diseases [RCV002841055] Chr13:94286394 [GRCh38]
Chr13:94938648 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1227C>T (p.Asp409=) single nucleotide variant not provided [RCV003099002] Chr13:94382488 [GRCh38]
Chr13:95034742 [GRCh37]
Chr13:13q31.3
likely benign
GRCh37/hg19 13q31.3(chr13:93784678-94407889)x3 copy number gain not provided [RCV002475613] Chr13:93784678..94407889 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.816C>T (p.Asn272=) single nucleotide variant not provided [RCV002591445] Chr13:94027833 [GRCh38]
Chr13:94680087 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.320-4G>T single nucleotide variant not provided [RCV002928161] Chr13:93830150 [GRCh38]
Chr13:94482403 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.435G>A (p.Glu145=) single nucleotide variant not provided [RCV003055739] Chr13:93830269 [GRCh38]
Chr13:94482522 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1217T>C (p.Ile406Thr) single nucleotide variant Inborn genetic diseases [RCV002637912]|not provided [RCV002637911] Chr13:94382478 [GRCh38]
Chr13:95034732 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1480G>A (p.Gly494Ser) single nucleotide variant Inborn genetic diseases [RCV002707501] Chr13:94403029 [GRCh38]
Chr13:95055283 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.329G>A (p.Arg110Gln) single nucleotide variant Inborn genetic diseases [RCV004632077]|not provided [RCV002795675] Chr13:93830163 [GRCh38]
Chr13:94482416 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1564C>T (p.Pro522Ser) single nucleotide variant not provided [RCV002570061] Chr13:94403113 [GRCh38]
Chr13:95055367 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.997G>A (p.Val333Met) single nucleotide variant Inborn genetic diseases [RCV002692392] Chr13:94286468 [GRCh38]
Chr13:94938722 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1466-6C>T single nucleotide variant Inborn genetic diseases [RCV002707035] Chr13:94403009 [GRCh38]
Chr13:95055263 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1510G>T (p.Asp504Tyr) single nucleotide variant not provided [RCV002796190] Chr13:94403059 [GRCh38]
Chr13:95055313 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1605C>T (p.Gly535=) single nucleotide variant not provided [RCV003008361] Chr13:94403154 [GRCh38]
Chr13:95055408 [GRCh37]
Chr13:13q32.1
likely benign
NM_005708.5(GPC6):c.283C>T (p.Arg95Cys) single nucleotide variant not provided [RCV002766862] Chr13:93545385 [GRCh38]
Chr13:94197638 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.301A>G (p.Arg101Gly) single nucleotide variant Inborn genetic diseases [RCV002830758] Chr13:93545403 [GRCh38]
Chr13:94197656 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.877+13T>C single nucleotide variant not provided [RCV002627077] Chr13:94027907 [GRCh38]
Chr13:94680161 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.285C>A (p.Arg95=) single nucleotide variant not provided [RCV002575094] Chr13:93545387 [GRCh38]
Chr13:94197640 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.455G>C (p.Gly152Ala) single nucleotide variant not provided [RCV002741696] Chr13:93830289 [GRCh38]
Chr13:94482542 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.606C>T (p.Asp202=) single nucleotide variant not provided [RCV002805624] Chr13:93830440 [GRCh38]
Chr13:94482693 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.634A>T (p.Thr212Ser) single nucleotide variant Inborn genetic diseases [RCV002697654] Chr13:93830468 [GRCh38]
Chr13:94482721 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1465+14T>A single nucleotide variant not provided [RCV002872401] Chr13:94398655 [GRCh38]
Chr13:95050909 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.500G>A (p.Arg167Gln) single nucleotide variant not provided [RCV002766927] Chr13:93830334 [GRCh38]
Chr13:94482587 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1466-17C>T single nucleotide variant not provided [RCV002593490] Chr13:94402998 [GRCh38]
Chr13:95055252 [GRCh37]
Chr13:13q32.1
likely benign
NM_005708.5(GPC6):c.1179G>A (p.Lys393=) single nucleotide variant not provided [RCV002721273] Chr13:94382440 [GRCh38]
Chr13:95034694 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.852C>T (p.Leu284=) single nucleotide variant not provided [RCV002628050] Chr13:94027869 [GRCh38]
Chr13:94680123 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1513G>A (p.Val505Met) single nucleotide variant Inborn genetic diseases [RCV002960987] Chr13:94403062 [GRCh38]
Chr13:95055316 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1556C>T (p.Ala519Val) single nucleotide variant Inborn genetic diseases [RCV002717585] Chr13:94403105 [GRCh38]
Chr13:95055359 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.639C>T (p.Arg213=) single nucleotide variant not provided [RCV003060564] Chr13:93830473 [GRCh38]
Chr13:94482726 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.331G>A (p.Glu111Lys) single nucleotide variant Inborn genetic diseases [RCV002934802] Chr13:93830165 [GRCh38]
Chr13:94482418 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1310A>G (p.Asn437Ser) single nucleotide variant Inborn genetic diseases [RCV002897479] Chr13:94398486 [GRCh38]
Chr13:95050740 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1403G>A (p.Arg468His) single nucleotide variant not provided [RCV003064828] Chr13:94398579 [GRCh38]
Chr13:95050833 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.64G>C (p.Gly22Arg) single nucleotide variant not provided [RCV002602263] Chr13:93227520 [GRCh38]
Chr13:93879773 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1239A>G (p.Thr413=) single nucleotide variant not provided [RCV002898891] Chr13:94382500 [GRCh38]
Chr13:95034754 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1241C>T (p.Ala414Val) single nucleotide variant not provided [RCV003086078] Chr13:94382502 [GRCh38]
Chr13:95034756 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.950T>C (p.Val317Ala) single nucleotide variant not provided [RCV002584466] Chr13:94286421 [GRCh38]
Chr13:94938675 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1643T>C (p.Leu548Pro) single nucleotide variant Inborn genetic diseases [RCV004066821]|not provided [RCV002654305] Chr13:94403192 [GRCh38]
Chr13:95055446 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.113G>C (p.Gly38Ala) single nucleotide variant not provided [RCV002604394] Chr13:93227569 [GRCh38]
Chr13:93879822 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1254C>T (p.Asn418=) single nucleotide variant not provided [RCV002943790] Chr13:94382515 [GRCh38]
Chr13:95034769 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.269C>T (p.Thr90Ile) single nucleotide variant Inborn genetic diseases [RCV002678937] Chr13:93545371 [GRCh38]
Chr13:94197624 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1290-12T>C single nucleotide variant not provided [RCV002586301] Chr13:94398454 [GRCh38]
Chr13:95050708 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1466-10T>C single nucleotide variant not provided [RCV002606179] Chr13:94403005 [GRCh38]
Chr13:95055259 [GRCh37]
Chr13:13q32.1
likely benign
NM_005708.5(GPC6):c.421G>C (p.Asp141His) single nucleotide variant not provided [RCV002654134] Chr13:93830255 [GRCh38]
Chr13:94482508 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1184C>A (p.Ser395Tyr) single nucleotide variant not provided [RCV002814458] Chr13:94382445 [GRCh38]
Chr13:95034699 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.694G>A (p.Ala232Thr) single nucleotide variant not provided [RCV003052749] Chr13:93830528 [GRCh38]
Chr13:94482781 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.646A>G (p.Ile216Val) single nucleotide variant Inborn genetic diseases [RCV004632008]|not provided [RCV002584041] Chr13:93830480 [GRCh38]
Chr13:94482733 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.814A>C (p.Asn272His) single nucleotide variant Inborn genetic diseases [RCV003215558] Chr13:94027831 [GRCh38]
Chr13:94680085 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1244G>A (p.Gly415Asp) single nucleotide variant Inborn genetic diseases [RCV003260895] Chr13:94382505 [GRCh38]
Chr13:95034759 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1466G>C (p.Ser489Thr) single nucleotide variant Inborn genetic diseases [RCV003373612] Chr13:94403015 [GRCh38]
Chr13:95055269 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.776G>A (p.Gly259Glu) single nucleotide variant Inborn genetic diseases [RCV003373904] Chr13:94027793 [GRCh38]
Chr13:94680047 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1083T>C (p.Asn361=) single nucleotide variant not provided [RCV003873922] Chr13:94306054 [GRCh38]
Chr13:94958308 [GRCh37]
Chr13:13q31.3
likely benign
GRCh37/hg19 13q21.33-33.1(chr13:73132193-104595598)x1 copy number loss not provided [RCV003483190] Chr13:73132193..104595598 [GRCh37]
Chr13:13q21.33-33.1
pathogenic
GRCh37/hg19 13q31.2-33.2(chr13:89012420-106371634)x1 copy number loss not provided [RCV003483195] Chr13:89012420..106371634 [GRCh37]
Chr13:13q31.2-33.2
pathogenic
GRCh37/hg19 13q21.2-34(chr13:61534068-115107733)x3 copy number gain not provided [RCV003484899] Chr13:61534068..115107733 [GRCh37]
Chr13:13q21.2-34
pathogenic
GRCh37/hg19 13q31.1-34(chr13:82131211-115107733)x1 copy number loss not provided [RCV003483192] Chr13:82131211..115107733 [GRCh37]
Chr13:13q31.1-34
pathogenic
GRCh37/hg19 13q22.1-34(chr13:73488238-115107733)x3 copy number gain not provided [RCV003484901] Chr13:73488238..115107733 [GRCh37]
Chr13:13q22.1-34
pathogenic
GRCh37/hg19 13q31.3-32.1(chr13:94064930-95288392)x3 copy number gain not provided [RCV003484903] Chr13:94064930..95288392 [GRCh37]
Chr13:13q31.3-32.1
uncertain significance
NM_005708.5(GPC6):c.594G>A (p.Lys198=) single nucleotide variant not provided [RCV003545908] Chr13:93830428 [GRCh38]
Chr13:94482681 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.24G>C (p.Val8=) single nucleotide variant not provided [RCV003665375] Chr13:93227480 [GRCh38]
Chr13:93879733 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1245C>T (p.Gly415=) single nucleotide variant not provided [RCV003852156] Chr13:94382506 [GRCh38]
Chr13:95034760 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.877+8G>T single nucleotide variant not provided [RCV003698524] Chr13:94027902 [GRCh38]
Chr13:94680156 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.161-7A>G single nucleotide variant not provided [RCV003817203] Chr13:93545256 [GRCh38]
Chr13:94197509 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1133G>A (p.Gly378Asp) single nucleotide variant not provided [RCV003854969] Chr13:94306104 [GRCh38]
Chr13:94958358 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1320C>T (p.Leu440=) single nucleotide variant not provided [RCV003848373] Chr13:94398496 [GRCh38]
Chr13:95050750 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.60C>T (p.Pro20=) single nucleotide variant not provided [RCV003866911] Chr13:93227516 [GRCh38]
Chr13:93879769 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.130C>T (p.Leu44=) single nucleotide variant not provided [RCV003684759] Chr13:93227586 [GRCh38]
Chr13:93879839 [GRCh37]
Chr13:13q31.3
likely benign
GRCh37/hg19 13q31.1-34(chr13:84669397-115107733)x1 copy number loss not specified [RCV003987038] Chr13:84669397..115107733 [GRCh37]
Chr13:13q31.1-34
pathogenic
GRCh37/hg19 13q31.1-34(chr13:82876219-115107733)x3 copy number gain not specified [RCV003987023] Chr13:82876219..115107733 [GRCh37]
Chr13:13q31.1-34
pathogenic
NM_005708.5(GPC6):c.729G>A (p.Gly243=) single nucleotide variant not provided [RCV003853963] Chr13:94027746 [GRCh38]
Chr13:94680000 [GRCh37]
Chr13:13q31.3
likely benign
GRCh37/hg19 13q14.2-32.2(chr13:49547974-98214905)x1 copy number loss not specified [RCV003987008] Chr13:49547974..98214905 [GRCh37]
Chr13:13q14.2-32.2
pathogenic
GRCh37/hg19 13q21.31-33.1(chr13:64825656-103641349)x1 copy number loss not specified [RCV003987009] Chr13:64825656..103641349 [GRCh37]
Chr13:13q21.31-33.1
pathogenic
NM_005708.5(GPC6):c.672G>A (p.Gly224=) single nucleotide variant not provided [RCV003708394] Chr13:93830506 [GRCh38]
Chr13:94482759 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1233C>T (p.Ser411=) single nucleotide variant not provided [RCV003733970] Chr13:94382494 [GRCh38]
Chr13:95034748 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1290-8C>T single nucleotide variant not provided [RCV003704269] Chr13:94398458 [GRCh38]
Chr13:95050712 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.387C>T (p.Gly129=) single nucleotide variant GPC6-related disorder [RCV003924680] Chr13:93830221 [GRCh38]
Chr13:94482474 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.714C>G (p.Val238=) single nucleotide variant GPC6-related disorder [RCV003919756] Chr13:94027731 [GRCh38]
Chr13:94679985 [GRCh37]
Chr13:13q31.3
likely benign
NM_005708.5(GPC6):c.1324A>C (p.Asn442His) single nucleotide variant Inborn genetic diseases [RCV004388120] Chr13:94398500 [GRCh38]
Chr13:95050754 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1580T>C (p.Val527Ala) single nucleotide variant Inborn genetic diseases [RCV004388121] Chr13:94403129 [GRCh38]
Chr13:95055383 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.334C>T (p.Leu112Phe) single nucleotide variant Inborn genetic diseases [RCV004388122] Chr13:93830168 [GRCh38]
Chr13:94482421 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.775G>C (p.Gly259Arg) single nucleotide variant Inborn genetic diseases [RCV004388123] Chr13:94027792 [GRCh38]
Chr13:94680046 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1076A>G (p.Asn359Ser) single nucleotide variant Inborn genetic diseases [RCV004632266] Chr13:94306047 [GRCh38]
Chr13:94958301 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1213A>G (p.Thr405Ala) single nucleotide variant Inborn genetic diseases [RCV004632268] Chr13:94382474 [GRCh38]
Chr13:95034728 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1009G>T (p.Val337Phe) single nucleotide variant Inborn genetic diseases [RCV004632269] Chr13:94305980 [GRCh38]
Chr13:94958234 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.817G>C (p.Val273Leu) single nucleotide variant Inborn genetic diseases [RCV004632270] Chr13:94027834 [GRCh38]
Chr13:94680088 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1273G>A (p.Gly425Arg) single nucleotide variant Inborn genetic diseases [RCV004632271] Chr13:94382534 [GRCh38]
Chr13:95034788 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.718C>A (p.Pro240Thr) single nucleotide variant Inborn genetic diseases [RCV004632272] Chr13:94027735 [GRCh38]
Chr13:94679989 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1481G>C (p.Gly494Ala) single nucleotide variant Inborn genetic diseases [RCV004982718] Chr13:94403030 [GRCh38]
Chr13:95055284 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.1562A>T (p.Asp521Val) single nucleotide variant Inborn genetic diseases [RCV004983765] Chr13:94403111 [GRCh38]
Chr13:95055365 [GRCh37]
Chr13:13q32.1
uncertain significance
NM_005708.5(GPC6):c.763C>T (p.Pro255Ser) single nucleotide variant Inborn genetic diseases [RCV004982720] Chr13:94027780 [GRCh38]
Chr13:94680034 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1196G>C (p.Trp399Ser) single nucleotide variant Inborn genetic diseases [RCV004982722] Chr13:94382457 [GRCh38]
Chr13:95034711 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.683G>A (p.Gly228Asp) single nucleotide variant Inborn genetic diseases [RCV004982721] Chr13:93830517 [GRCh38]
Chr13:94482770 [GRCh37]
Chr13:13q31.3
uncertain significance
GRCh38/hg38 13q11-34(chr13:18445862-114327173)x1 copy number loss See cases [RCV000135610] Chr13:18445862..114327173 [GRCh38]
Chr13:19020001..115085141 [GRCh37]
Chr13:10098739..114110750 [NCBI36]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3 copy number gain See cases [RCV000240150] Chr13:19571503..115092569 [GRCh37]
Chr13:13q12.11-34
pathogenic
GRCh37/hg19 13q11-34(chr13:19436287-115107733) copy number gain See cases [RCV000510405] Chr13:19436287..115107733 [GRCh37]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q11-34(chr13:19031237-115107157)x3 copy number gain not provided [RCV000750643] Chr13:19031237..115107157 [GRCh37]
Chr13:13q11-34
pathogenic
GRCh37/hg19 13q31.3(chr13:94120662-94430587)x1 copy number loss not provided [RCV000847887] Chr13:94120662..94430587 [GRCh37]
Chr13:13q31.3
pathogenic
NM_005708.5(GPC6):c.711+91_711+93del deletion not provided [RCV001675333] Chr13:93830613..93830615 [GRCh38]
Chr13:94482866..94482868 [GRCh37]
Chr13:13q31.3
benign
NM_005708.5(GPC6):c.20C>A (p.Ala7Asp) single nucleotide variant not provided [RCV001904271] Chr13:93227476 [GRCh38]
Chr13:93879729 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1466-18T>G single nucleotide variant not provided [RCV002663588] Chr13:94402997 [GRCh38]
Chr13:95055251 [GRCh37]
Chr13:13q32.1
likely benign
NM_005708.5(GPC6):c.881C>G (p.Ala294Gly) single nucleotide variant Inborn genetic diseases [RCV003356544] Chr13:94286352 [GRCh38]
Chr13:94938606 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.49C>T (p.Leu17Phe) single nucleotide variant Autosomal recessive omodysplasia [RCV003990677] Chr13:93227505 [GRCh38]
Chr13:93879758 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1193T>G (p.Val398Gly) single nucleotide variant Autosomal recessive omodysplasia [RCV003990767] Chr13:94382454 [GRCh38]
Chr13:95034708 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.866A>G (p.Asn289Ser) single nucleotide variant Inborn genetic diseases [RCV004388124] Chr13:94027883 [GRCh38]
Chr13:94680137 [GRCh37]
Chr13:13q31.3
uncertain significance
NM_005708.5(GPC6):c.1054T>A (p.Ser352Thr) single nucleotide variant Inborn genetic diseases [RCV004982719] Chr13:94306025 [GRCh38]
Chr13:94958279 [GRCh37]
Chr13:13q31.3
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1278
Count of miRNA genes:687
Interacting mature miRNAs:798
Transcripts:ENST00000377047
Prediction methods:Microtar, Miranda, 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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
596974357GWAS1093876_Hmajor depressive disorder QTL GWAS1093876 (human)4e-09major depressive disorder139335705993357060Human
597075479GWAS1171553_Hheel bone mineral density QTL GWAS1171553 (human)6e-09heel bone mineral densitybone mineral density (CMO:0001226)139324644493246445Human
407022401GWAS671377_Hmental or behavioural disorder QTL GWAS671377 (human)0.000009mental or behavioural disorder139368884393688844Human
597173406GWAS1269480_Heducational attainment QTL GWAS1269480 (human)1e-08educational attainment139328645393286454Human
597252767GWAS1348841_Hinsomnia, total blood protein measurement QTL GWAS1348841 (human)5e-09insomnia, total blood protein measurementblood protein measurement (CMO:0000028)139405612994056130Human
597173407GWAS1269481_Heducational attainment QTL GWAS1269481 (human)2e-09educational attainment139346113693461137Human
597601428GWAS1658288_Hcreatinine measurement QTL GWAS1658288 (human)7e-08creatinine measurementblood creatinine measurement (CMO:0000767)139437350194373502Human
597027737GWAS1123811_Hwaist-hip ratio QTL GWAS1123811 (human)2e-09waist-hip ratiowaist to hip ratio (WHR) (CMO:0000020)139324468293244683Human
406942797GWAS591773_Hheel bone mineral density QTL GWAS591773 (human)8e-31heel bone mineral densitybone mineral density (CMO:0001226)139341469993414700Human
597603219GWAS1660079_Htype 2 diabetes mellitus QTL GWAS1660079 (human)3e-10type 2 diabetes mellitus139400831594008316Human
597296660GWAS1392734_Hblood chromium measurement QTL GWAS1392734 (human)0.000002blood chromium measurement139373491093734911Human
406942798GWAS591774_Hheel bone mineral density QTL GWAS591774 (human)9e-22heel bone mineral densitybone mineral density (CMO:0001226)139372788393727884Human
597313162GWAS1409236_Hvaginal microbiome measurement QTL GWAS1409236 (human)0.000004vaginal microbiome measurement139347457293474573Human
597433740GWAS1529814_Hprotein measurement QTL GWAS1529814 (human)3e-28protein measurement139438539294385393Human
597601550GWAS1658410_Hcitrate measurement QTL GWAS1658410 (human)0.000002citrate measurement139438722894387229Human
596970247GWAS1089766_Hlate-onset Alzheimers disease QTL GWAS1089766 (human)0.0000006late-onset Alzheimers disease139350754793507548Human
597193738GWAS1289812_Hmemory performance QTL GWAS1289812 (human)0.000004memory performance139437919494379195Human
597148302GWAS1244376_Hsmoking initiation QTL GWAS1244376 (human)3e-22smoking initiation139326347793263478Human
597164675GWAS1260749_Hlipid measurement QTL GWAS1260749 (human)0.000009lipid measurementblood lipid measurement (CMO:0000050)139359282093592821Human
407124955GWAS773931_HAlzheimer disease QTL GWAS773931 (human)7e-08Alzheimer disease139329360593293606Human
597204923GWAS1300997_Hwellbeing measurement QTL GWAS1300997 (human)6e-10wellness/fitness trait (VT:1000152)139338878293388783Human
597226174GWAS1322248_Hchronotype measurement QTL GWAS1322248 (human)6e-14chronotype measurement139340984293409843Human
597204017GWAS1300091_Hwellbeing measurement QTL GWAS1300091 (human)5e-10wellness/fitness trait (VT:1000152)139338878293388783Human
597056703GWAS1152777_Hmetabolic syndrome QTL GWAS1152777 (human)2e-10metabolic syndrome139345794593457946Human
597090111GWAS1186185_Hnon-alcoholic fatty liver disease QTL GWAS1186185 (human)0.000001non-alcoholic fatty liver disease139436738494367385Human
407020136GWAS669112_Hneurotic disorder, age at assessment QTL GWAS669112 (human)0.0000001neurotic disorder, age at assessment139335891693358917Human
597137341GWAS1233415_Hdiastolic blood pressure, systolic blood pressure QTL GWAS1233415 (human)6e-08diastolic blood pressure, systolic blood pressuresystolic blood pressure (CMO:0000004)139376374893763749Human
597219250GWAS1315324_Hbody height QTL GWAS1315324 (human)6e-21body height (VT:0001253)body height (CMO:0000106)139393610593936106Human
407099240GWAS748216_Hunipolar depression QTL GWAS748216 (human)4e-09unipolar depression139335705993357060Human
597288242GWAS1384316_Hbody weight QTL GWAS1384316 (human)2e-08body mass (VT:0001259)body weight (CMO:0000012)139344982193449822Human
407080300GWAS729276_Hwaist-hip ratio QTL GWAS729276 (human)5e-08waist-hip ratiowaist to hip ratio (WHR) (CMO:0000020)139326073793260738Human
2289426BW213_HBody weight QTL 213 (human)2.780.0002Body weightBMI1384267977110267977Human
597334057GWAS1430131_HS-warfarin to R-warfarin ratio measurement QTL GWAS1430131 (human)0.000009S-warfarin to R-warfarin ratio measurement139329328493293285Human
407023095GWAS672071_Hrenal sinus adipose tissue measurement QTL GWAS672071 (human)0.000006renal sinus adipose tissue measurement139421851194218512Human
597229359GWAS1325433_Hheel bone mineral density QTL GWAS1325433 (human)4e-21heel bone mineral densitybone mineral density (CMO:0001226)139324644493246445Human
597173408GWAS1269482_Heducational attainment QTL GWAS1269482 (human)0.000001educational attainment139415198994151990Human
406968569GWAS617545_Hsleep quality QTL GWAS617545 (human)0.000007sleep quality139428805594288056Human
2289433BW340_HBody weight QTL 340 (human)3.11Body morphometrywaist circumference1384267977110267977Human
597616674GWAS1673534_HLower limb asymmetry QTL GWAS1673534 (human)4e-11Lower limb asymmetry139329140693291407Human
407028735GWAS677711_Hlumbar disc degeneration QTL GWAS677711 (human)0.0000009lumbar disc degeneration139430057894300579Human
597447459GWAS1543533_Hcarotid artery intima media thickness QTL GWAS1543533 (human)0.000001carotid artery intima media thickness139417436694174367Human
597319898GWAS1415972_Hsmoking initiation QTL GWAS1415972 (human)6e-22smoking initiation139323357793233578Human
407046019GWAS694995_Hbody composition measurement QTL GWAS694995 (human)0.0000007body composition measurement139358087693580877Human
597211864GWAS1307938_Harterial stiffness measurement QTL GWAS1307938 (human)0.000001arterial stiffness measurementpulse wave velocity (CMO:0003717)139435123294351233Human
597319899GWAS1415973_Hsmoking initiation QTL GWAS1415973 (human)1e-10smoking initiation139345368493453685Human
597187930GWAS1284004_Hmajor depressive disorder QTL GWAS1284004 (human)4e-09major depressive disorder139335705993357060Human
597045973GWAS1142047_HAbnormality of refraction QTL GWAS1142047 (human)4e-23Abnormality of refraction139326053293260533Human
597183196GWAS1279270_Hbody mass index QTL GWAS1279270 (human)5e-09body mass indexbody mass index (BMI) (CMO:0000105)139347190093471901Human
407027462GWAS676438_Hbody composition measurement QTL GWAS676438 (human)0.0000004body composition measurement139358087693580877Human
596961490GWAS1081009_Hmetabolic syndrome QTL GWAS1081009 (human)2e-10metabolic syndrome139345794593457946Human
597051985GWAS1148059_Hchronotype measurement QTL GWAS1148059 (human)8e-09chronotype measurement139344696493446965Human
597102939GWAS1199013_Hmitochondrial DNA measurement QTL GWAS1199013 (human)0.0000009mitochondrial DNA measurement139332339093323391Human
597119835GWAS1215909_HAlzheimer disease QTL GWAS1215909 (human)0.0000004Alzheimer disease139350754793507548Human
597160539GWAS1256613_Hlipid measurement QTL GWAS1256613 (human)0.000004lipid measurementblood lipid measurement (CMO:0000050)139360621793606218Human
597331926GWAS1428000_Hcolorectal cancer QTL GWAS1428000 (human)0.0000005colorectal cancer139426628194266282Human
597536848GWAS1632922_Hbody height QTL GWAS1632922 (human)2e-25body height (VT:0001253)body height (CMO:0000106)139322486493224865Human
597119066GWAS1215140_Hbiological sex QTL GWAS1215140 (human)2e-08biological sex139395873393958734Human
597093570GWAS1189644_Hschizophrenia QTL GWAS1189644 (human)0.0000003schizophrenia139377410093774101Human
596966209GWAS1085728_Hlate-onset Alzheimers disease QTL GWAS1085728 (human)0.000003late-onset Alzheimers disease139350754793507548Human
597318733GWAS1414807_Hdiastolic blood pressure, systolic blood pressure QTL GWAS1414807 (human)2e-08diastolic blood pressure, systolic blood pressuresystolic blood pressure (CMO:0000004)139376374893763749Human
597134400GWAS1230474_Hfat body mass QTL GWAS1230474 (human)2e-08body fat mass (VT:0010482)total body fat mass (CMO:0000305)139415369794153698Human
597225536GWAS1321610_Hheel bone mineral density QTL GWAS1321610 (human)2e-12heel bone mineral densitybone mineral density (CMO:0001226)139332644493326445Human
597433413GWAS1529487_Hprotein measurement QTL GWAS1529487 (human)2e-15protein measurement139323496493234965Human
597225537GWAS1321611_Hheel bone mineral density QTL GWAS1321611 (human)3e-18heel bone mineral densitybone mineral density (CMO:0001226)139336355293363553Human
597225538GWAS1321612_Hheel bone mineral density QTL GWAS1321612 (human)4e-28heel bone mineral densitybone mineral density (CMO:0001226)139341469993414700Human
407028638GWAS677614_Hvisceral adipose tissue measurement QTL GWAS677614 (human)0.000004visceral adipose tissue measurementabdominal fat morphological measurement (CMO:0000311)139328645393286454Human
597200068GWAS1296142_Hlate-onset Alzheimers disease QTL GWAS1296142 (human)0.0000006late-onset Alzheimers disease139350754793507548Human
597208262GWAS1304336_Hwellbeing measurement QTL GWAS1304336 (human)5e-09wellness/fitness trait (VT:1000152)139340183793401838Human
597277948GWAS1374022_Hinsomnia QTL GWAS1374022 (human)3e-09insomnia139341293393412934Human
597380339GWAS1476413_Hresponse to reverse transcriptase inhibitor, HIV-1 infection, peripheral neuropathy QTL GWAS1476413 (human)0.0000002response to viral infection trait (VT:0010439)139322677893226779Human
597207409GWAS1303483_Hneuroticism measurement QTL GWAS1303483 (human)4e-10depressive symptom measurement139338878293388783Human
407041961GWAS690937_Hserum dimethylarginine measurement QTL GWAS690937 (human)0.000007serum dimethylarginine measurement139355639693556397Human
597071866GWAS1167940_Hfacial height measurement QTL GWAS1167940 (human)0.0000001facial morphology trait (VT:0003743)139433119194331192Human
407078830GWAS727806_HBMI-adjusted waist-hip ratio QTL GWAS727806 (human)3e-08body size trait (VT:0100005)139326073793260738Human
407024815GWAS673791_Hattention deficit hyperactivity disorder QTL GWAS673791 (human)1e-08attention deficit hyperactivity disorder139375625393756254Human
597323882GWAS1419956_Hinsomnia QTL GWAS1419956 (human)8e-11insomnia139333840193338402Human
597034726GWAS1130800_Hheel bone mineral density QTL GWAS1130800 (human)2e-22heel bone mineral densitybone mineral density (CMO:0001226)139372788393727884Human
597323883GWAS1419957_Hinsomnia QTL GWAS1419957 (human)4e-10insomnia139340007093400071Human
407060018GWAS708994_Hchronotype measurement QTL GWAS708994 (human)1e-09chronotype measurement139345959093459591Human
597199849GWAS1295923_Hlate-onset Alzheimers disease QTL GWAS1295923 (human)0.000003late-onset Alzheimers disease139350754793507548Human
597034724GWAS1130798_Hheel bone mineral density QTL GWAS1130798 (human)8e-35heel bone mineral densitybone mineral density (CMO:0001226)139341469993414700Human
597034725GWAS1130799_Hheel bone mineral density QTL GWAS1130799 (human)6e-10heel bone mineral densitybone mineral density (CMO:0001226)139343192893431929Human
597034722GWAS1130796_Hheel bone mineral density QTL GWAS1130796 (human)8e-16heel bone mineral densitybone mineral density (CMO:0001226)139335984793359848Human
597034723GWAS1130797_Hheel bone mineral density QTL GWAS1130797 (human)2e-14heel bone mineral densitybone mineral density (CMO:0001226)139336522393365224Human
597330415GWAS1426489_Hsleep duration QTL GWAS1426489 (human)0.000005sleep duration139418554494185545Human
597044449GWAS1140523_Hrefractive error QTL GWAS1140523 (human)7e-09refractive error139337564093375641Human
597129710GWAS1225784_Hpulse pressure measurement QTL GWAS1225784 (human)7e-09pulse pressure measurementpulse pressure (CMO:0000292)139376562093765621Human
597178724GWAS1274798_Hglypican-6 measurement QTL GWAS1274798 (human)8e-14glypican-6 measurement139323143493231435Human
597338596GWAS1434670_Hage at diagnosis, osteonecrosis QTL GWAS1434670 (human)0.000002age at diagnosis, osteonecrosis139355132193551322Human
597178726GWAS1274800_Hglypican-6 measurement QTL GWAS1274800 (human)2e-12glypican-6 measurement139438249594382496Human
597615969GWAS1672829_Hglomerulonephritis QTL GWAS1672829 (human)2e-11glomerulonephritis139425208694252087Human

Markers in Region
D13S71  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,978,440 - 94,978,512UniSTSGRCh37
Build 361393,776,441 - 93,776,513RGDNCBI36
Celera1375,826,819 - 75,826,891RGD
Cytogenetic Map13q32UniSTS
HuRef1375,575,535 - 75,575,613UniSTS
Marshfield Genetic Map1373.04UniSTS
Marshfield Genetic Map1373.04RGD
deCODE Assembly Map1385.75UniSTS
D13S775  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,763,693 - 94,763,866UniSTSGRCh37
Build 361393,561,694 - 93,561,867RGDNCBI36
Celera1375,612,079 - 75,612,246RGD
Cytogenetic Map13q32UniSTS
HuRef1375,360,706 - 75,360,873UniSTS
Marshfield Genetic Map1373.04RGD
Marshfield Genetic Map1373.04UniSTS
deCODE Assembly Map1385.0UniSTS
Whitehead-YAC Contig Map13 UniSTS
D13S167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,676,235 - 94,676,420UniSTSGRCh37
Build 361393,474,236 - 93,474,421RGDNCBI36
Celera1375,524,646 - 75,524,831RGD
Cytogenetic Map13q32UniSTS
HuRef1375,273,274 - 75,273,459UniSTS
Marshfield Genetic Map1373.04UniSTS
Marshfield Genetic Map1373.04RGD
Genethon Genetic Map1375.8UniSTS
GeneMap99-GB4 RH Map13264.2UniSTS
Whitehead-RH Map13245.2UniSTS
Whitehead-YAC Contig Map13 UniSTS
NCBI RH Map13677.3UniSTS
D13S281  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,563,571 - 94,563,812UniSTSGRCh37
GRCh371394,563,610 - 94,563,783UniSTSGRCh37
Build 361393,361,611 - 93,361,784RGDNCBI36
Celera1375,412,028 - 75,412,201RGD
Celera1375,411,989 - 75,412,230UniSTS
Cytogenetic Map13q32UniSTS
HuRef1375,160,842 - 75,161,083UniSTS
HuRef1375,160,881 - 75,161,054UniSTS
Marshfield Genetic Map1373.04UniSTS
Marshfield Genetic Map1373.04RGD
Genethon Genetic Map1374.3UniSTS
TNG Radiation Hybrid Map1333714.0UniSTS
deCODE Assembly Map1384.68UniSTS
Stanford-G3 RH Map132677.0UniSTS
GeneMap99-GB4 RH Map13262.29UniSTS
Whitehead-RH Map13248.2UniSTS
Whitehead-YAC Contig Map13 UniSTS
NCBI RH Map13826.1UniSTS
GeneMap99-G3 RH Map132976.0UniSTS
RH65457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,000,897 - 95,001,069UniSTSGRCh37
Build 361393,798,898 - 93,799,070RGDNCBI36
Celera1375,849,278 - 75,849,450RGD
Cytogenetic Map13q32UniSTS
HuRef1375,598,001 - 75,598,173UniSTS
GeneMap99-GB4 RH Map13262.29UniSTS
D13S762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,435,592 - 94,435,908UniSTSGRCh37
Build 361393,233,593 - 93,233,909RGDNCBI36
Celera1375,284,040 - 75,284,356RGD
Cytogenetic Map13q32UniSTS
Whitehead-RH Map13245.2UniSTS
Whitehead-YAC Contig Map13 UniSTS
NCBI RH Map13677.3UniSTS
D13S1193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,039,847 - 94,040,047UniSTSGRCh37
Build 361392,837,848 - 92,838,048RGDNCBI36
Celera1374,888,253 - 74,888,453RGD
Cytogenetic Map13q32UniSTS
HuRef1374,636,836 - 74,637,036UniSTS
Whitehead-YAC Contig Map13 UniSTS
WI-18121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,541,121 - 94,541,260UniSTSGRCh37
Build 361393,339,122 - 93,339,261RGDNCBI36
Celera1375,389,540 - 75,389,679RGD
Cytogenetic Map13q32UniSTS
HuRef1375,138,415 - 75,138,554UniSTS
GeneMap99-GB4 RH Map13262.29UniSTS
Whitehead-RH Map13248.2UniSTS
D13S184E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,252,095 - 94,252,300UniSTSGRCh37
GRCh371394,252,047 - 94,252,129UniSTSGRCh37
Build 361393,050,096 - 93,050,301RGDNCBI36
Celera1375,100,484 - 75,100,689RGD
Celera1375,100,436 - 75,100,518UniSTS
HuRef1374,848,926 - 74,849,008UniSTS
HuRef1374,848,974 - 74,849,179UniSTS
RH98501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,101,001 - 94,101,091UniSTSGRCh37
Build 361392,899,002 - 92,899,092RGDNCBI36
Celera1374,949,399 - 74,949,489RGD
Cytogenetic Map13q32UniSTS
HuRef1374,698,006 - 74,698,096UniSTS
RH99121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,055,322 - 95,055,466UniSTSGRCh37
Build 361393,853,323 - 93,853,467RGDNCBI36
Celera1375,903,563 - 75,903,707RGD
Cytogenetic Map13q32UniSTS
HuRef1375,652,284 - 75,652,428UniSTS
GeneMap99-GB4 RH Map13262.29UniSTS
SHGC-58551  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,055,609 - 95,055,863UniSTSGRCh37
Build 361393,853,610 - 93,853,864RGDNCBI36
Celera1375,903,850 - 75,904,105RGD
Cytogenetic Map13q32UniSTS
HuRef1375,652,571 - 75,652,826UniSTS
TNG Radiation Hybrid Map1334013.0UniSTS
SHGC-79124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,825,723 - 94,826,028UniSTSGRCh37
Build 361393,623,724 - 93,624,029RGDNCBI36
Celera1375,674,094 - 75,674,399RGD
Cytogenetic Map13q32UniSTS
HuRef1375,422,716 - 75,423,021UniSTS
TNG Radiation Hybrid Map1333853.0UniSTS
SHGC-83667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,431,512 - 94,431,850UniSTSGRCh37
Build 361393,229,513 - 93,229,851RGDNCBI36
Celera1375,279,960 - 75,280,298RGD
Cytogenetic Map13q32UniSTS
HuRef1375,028,712 - 75,029,050UniSTS
TNG Radiation Hybrid Map1333623.0UniSTS
SHGC-78776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,245,555 - 94,245,883UniSTSGRCh37
Build 361393,043,556 - 93,043,884RGDNCBI36
Celera1375,093,945 - 75,094,273RGD
Cytogenetic Map13q32UniSTS
HuRef1374,842,437 - 74,842,765UniSTS
TNG Radiation Hybrid Map1334190.0UniSTS
SHGC-84554  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,012,451 - 94,012,750UniSTSGRCh37
Build 361392,810,452 - 92,810,751RGDNCBI36
Celera1374,860,858 - 74,861,157RGD
Cytogenetic Map13q32UniSTS
HuRef1374,609,571 - 74,609,870UniSTS
G49558  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,157,956 - 94,158,071UniSTSGRCh37
Build 361392,955,957 - 92,956,072RGDNCBI36
Celera1375,006,356 - 75,006,471RGD
Cytogenetic Map13q32UniSTS
HuRef1374,754,543 - 74,754,658UniSTS
TNG Radiation Hybrid Map1334267.0UniSTS
G49559  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,315,494 - 94,315,590UniSTSGRCh37
Build 361393,113,495 - 93,113,591RGDNCBI36
Celera1375,163,886 - 75,163,982RGD
Cytogenetic Map13q32UniSTS
HuRef1374,912,327 - 74,912,423UniSTS
TNG Radiation Hybrid Map1334125.0UniSTS
G60425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,676,241 - 94,676,468UniSTSGRCh37
Build 361393,474,242 - 93,474,469RGDNCBI36
Celera1375,524,652 - 75,524,879RGD
Cytogenetic Map13q32UniSTS
HuRef1375,273,280 - 75,273,507UniSTS
TNG Radiation Hybrid Map1333791.0UniSTS
TNG Radiation Hybrid Map4110044.0UniSTS
RH118850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,151,444 - 94,151,722UniSTSGRCh37
Build 361392,949,445 - 92,949,723RGDNCBI36
Celera1374,999,845 - 75,000,123RGD
Cytogenetic Map13q32UniSTS
HuRef1374,748,030 - 74,748,308UniSTS
G62575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,461,664 - 94,461,977UniSTSGRCh37
Build 361393,259,665 - 93,259,978RGDNCBI36
Celera1375,310,094 - 75,310,407RGD
Cytogenetic Map13q32UniSTS
HuRef1375,058,866 - 75,059,179UniSTS
TNG Radiation Hybrid Map1333628.0UniSTS
G62678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,501,786 - 94,502,130UniSTSGRCh37
Build 361393,299,787 - 93,300,131RGDNCBI36
Celera1375,350,205 - 75,350,549RGD
Cytogenetic Map13q32UniSTS
HuRef1375,099,088 - 75,099,432UniSTS
G63691  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,975,855 - 94,976,165UniSTSGRCh37
Build 361393,773,856 - 93,774,166RGDNCBI36
Celera1375,824,234 - 75,824,544RGD
Cytogenetic Map13q32UniSTS
HuRef1375,572,950 - 75,573,260UniSTS
TNG Radiation Hybrid Map1333941.0UniSTS
D13S125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,391,137 - 94,391,285UniSTSGRCh37
Build 361393,189,138 - 93,189,286RGDNCBI36
Celera1375,239,517 - 75,239,663RGD
Cytogenetic Map13q32UniSTS
HuRef1374,987,925 - 74,988,071UniSTS
D13S197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,923,561 - 94,923,685UniSTSGRCh37
Build 361393,721,562 - 93,721,686RGDNCBI36
Celera1375,771,940 - 75,772,064RGD
Cytogenetic Map13q32UniSTS
HuRef1375,520,491 - 75,520,613UniSTS
D13S1093E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,013,593 - 94,013,741UniSTSGRCh37
Build 361392,811,594 - 92,811,742RGDNCBI36
Celera1374,862,000 - 74,862,148RGD
Cytogenetic Map13q32UniSTS
HuRef1374,610,713 - 74,610,861UniSTS
SHGC-105244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,920,127 - 94,920,438UniSTSGRCh37
Build 361393,718,128 - 93,718,439RGDNCBI36
Celera1375,768,506 - 75,768,817RGD
Cytogenetic Map13q32UniSTS
HuRef1375,517,057 - 75,517,368UniSTS
TNG Radiation Hybrid Map1333897.0UniSTS
D13S129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,264,413 - 94,264,826UniSTSGRCh37
Build 361393,062,414 - 93,062,827RGDNCBI36
Celera1375,112,802 - 75,113,219RGD
Cytogenetic Map13q32UniSTS
HuRef1374,861,284 - 74,861,705UniSTS
Whitehead-YAC Contig Map13 UniSTS
A008V26  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,947,138 - 93,947,358UniSTSGRCh37
Build 361392,745,139 - 92,745,359RGDNCBI36
Celera1374,795,545 - 74,795,765RGD
Cytogenetic Map13q32UniSTS
HuRef1374,544,203 - 74,544,423UniSTS
GeneMap99-GB4 RH Map13264.31UniSTS
NCBI RH Map13806.7UniSTS
SHGC-106184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,005,079 - 95,005,359UniSTSGRCh37
Build 361393,803,080 - 93,803,360RGDNCBI36
Celera1375,853,460 - 75,853,740RGD
Cytogenetic Map13q32UniSTS
HuRef1375,602,183 - 75,602,463UniSTS
TNG Radiation Hybrid Map1333949.0UniSTS
SHGC-106880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,058,349 - 95,058,639UniSTSGRCh37
Build 361393,856,350 - 93,856,640RGDNCBI36
Celera1375,906,591 - 75,906,881RGD
Cytogenetic Map13q32UniSTS
HuRef1375,655,312 - 75,655,602UniSTS
TNG Radiation Hybrid Map1333995.0UniSTS
SHGC-155183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,287,235 - 94,287,581UniSTSGRCh37
Build 361393,085,236 - 93,085,582RGDNCBI36
Celera1375,135,632 - 75,135,978RGD
Cytogenetic Map13q32UniSTS
HuRef1374,884,114 - 74,884,460UniSTS
TNG Radiation Hybrid Map1334161.0UniSTS
SHGC-81838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,502,108 - 94,502,414UniSTSGRCh37
Build 361393,300,109 - 93,300,415RGDNCBI36
Celera1375,350,527 - 75,350,833RGD
Cytogenetic Map13q32UniSTS
HuRef1375,099,410 - 75,099,716UniSTS
TNG Radiation Hybrid Map1333642.0UniSTS
D13S1206  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,742,806 - 94,742,962UniSTSGRCh37
Build 361393,540,807 - 93,540,963RGDNCBI36
Celera1375,591,215 - 75,591,368RGD
Cytogenetic Map13q32UniSTS
HuRef1375,339,840 - 75,339,993UniSTS
Whitehead-RH Map13242.1UniSTS
Whitehead-YAC Contig Map13 UniSTS
NCBI RH Map13676.3UniSTS
D13S1665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,059,326 - 95,059,465UniSTSGRCh37
GRCh371395,059,457 - 95,059,603UniSTSGRCh37
Build 361393,857,458 - 93,857,604RGDNCBI36
Celera1375,907,699 - 75,907,845RGD
Celera1375,907,568 - 75,907,707UniSTS
Cytogenetic Map13q32UniSTS
HuRef1375,656,420 - 75,656,566UniSTS
HuRef1375,656,289 - 75,656,428UniSTS
TNG Radiation Hybrid Map1333995.0UniSTS
Stanford-G3 RH Map132684.0UniSTS
NCBI RH Map13874.2UniSTS
GeneMap99-G3 RH Map132983.0UniSTS
WI-17041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,840,613 - 94,840,762UniSTSGRCh37
Build 361393,638,614 - 93,638,763RGDNCBI36
Celera1375,688,994 - 75,689,143RGD
Cytogenetic Map13q32UniSTS
HuRef1375,437,623 - 75,437,772UniSTS
GeneMap99-GB4 RH Map13264.51UniSTS
Whitehead-RH Map13245.2UniSTS
NCBI RH Map13676.8UniSTS
GPC6__6647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,055,329 - 95,056,040UniSTSGRCh37
Build 361393,853,330 - 93,854,041RGDNCBI36
Celera1375,903,570 - 75,904,282RGD
HuRef1375,652,291 - 75,653,003UniSTS
D13S1635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,935,730 - 93,935,888UniSTSGRCh37
Build 361392,733,731 - 92,733,889RGDNCBI36
Celera1374,784,122 - 74,784,280RGD
HuRef1374,532,780 - 74,532,938UniSTS
D13S1636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,992,365 - 94,992,556UniSTSGRCh37
Build 361393,790,366 - 93,790,557RGDNCBI36
Celera1375,840,745 - 75,840,936RGD
HuRef1375,589,467 - 75,589,658UniSTS
RH44943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,288,215 - 94,288,332UniSTSGRCh37
Build 361393,086,216 - 93,086,333RGDNCBI36
Celera1375,136,612 - 75,136,729RGD
Cytogenetic Map13q32UniSTS
HuRef1374,885,094 - 74,885,211UniSTS
GeneMap99-GB4 RH Map13262.19UniSTS
NCBI RH Map13826.1UniSTS
RH44781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,059,394 - 95,059,569UniSTSGRCh37
Build 361393,857,395 - 93,857,570RGDNCBI36
Celera1375,907,636 - 75,907,811RGD
Cytogenetic Map13q32UniSTS
HuRef1375,656,357 - 75,656,532UniSTS
GeneMap99-GB4 RH Map13265.85UniSTS
D12S1283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,763,691 - 94,763,834UniSTSGRCh37
Build 361393,561,692 - 93,561,835RGDNCBI36
Celera1375,612,077 - 75,612,214RGD
Cytogenetic Map13q32UniSTS
HuRef1375,360,704 - 75,360,841UniSTS
RH68496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,057,038 - 95,057,159UniSTSGRCh37
Build 361393,855,039 - 93,855,160RGDNCBI36
Celera1375,905,280 - 75,905,401RGD
Cytogenetic Map13q32UniSTS
HuRef1375,654,001 - 75,654,122UniSTS
GeneMap99-GB4 RH Map13262.29UniSTS
RH44643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,947,103 - 93,947,224UniSTSGRCh37
Build 361392,745,104 - 92,745,225RGDNCBI36
Celera1374,795,510 - 74,795,631RGD
Cytogenetic Map13q32UniSTS
HuRef1374,544,168 - 74,544,289UniSTS
GeneMap99-GB4 RH Map13262.29UniSTS
ATC-P10376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,076,838 - 94,076,937UniSTSGRCh37
Build 361392,874,839 - 92,874,938RGDNCBI36
Celera1374,925,234 - 74,925,333RGD
Cytogenetic Map13q32UniSTS
HuRef1374,673,821 - 74,673,929UniSTS
Whitehead-YAC Contig Map13 UniSTS
STS-AA007180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,012,743 - 94,012,915UniSTSGRCh37
Build 361392,810,744 - 92,810,916RGDNCBI36
Celera1374,861,150 - 74,861,322RGD
Cytogenetic Map13q32UniSTS
HuRef1374,609,863 - 74,610,035UniSTS
GeneMap99-GB4 RH Map13264.51UniSTS
RH45636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,421,952 - 94,422,115UniSTSGRCh37
Build 361393,219,953 - 93,220,116RGDNCBI36
Celera1375,270,401 - 75,270,564RGD
Cytogenetic Map13q32UniSTS
HuRef1375,019,153 - 75,019,316UniSTS
GeneMap99-GB4 RH Map13262.29UniSTS
WI-18223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,115,379 - 94,115,516UniSTSGRCh37
Build 361392,913,380 - 92,913,517RGDNCBI36
Celera1374,963,777 - 74,963,914RGD
Cytogenetic Map13q32UniSTS
HuRef1374,712,036 - 74,712,173UniSTS
GeneMap99-GB4 RH Map13262.19UniSTS
Whitehead-RH Map13248.2UniSTS
NCBI RH Map13826.1UniSTS
D13S1451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,462,575 - 94,462,752UniSTSGRCh37
Build 361393,260,576 - 93,260,753RGDNCBI36
Celera1375,311,005 - 75,311,182RGD
Cytogenetic Map13q32UniSTS
HuRef1375,059,777 - 75,059,954UniSTS
Whitehead-RH Map13248.2UniSTS
Whitehead-YAC Contig Map13 UniSTS
NCBI RH Map13826.1UniSTS
WI-20311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371395,059,344 - 95,059,602UniSTSGRCh37
Build 361393,857,345 - 93,857,603RGDNCBI36
Celera1375,907,586 - 75,907,844RGD
Cytogenetic Map13q32UniSTS
HuRef1375,656,307 - 75,656,565UniSTS
GeneMap99-GB4 RH Map13264.24UniSTS
Whitehead-RH Map13249.8UniSTS
SHGC-58318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371394,707,177 - 94,707,448UniSTSGRCh37
Build 361393,505,178 - 93,505,449RGDNCBI36
Celera1375,555,592 - 75,555,863RGD
Cytogenetic Map13q32UniSTS
HuRef1375,304,226 - 75,304,497UniSTS
TNG Radiation Hybrid Map1333803.0UniSTS
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
GPC6  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,879,722 - 93,879,836UniSTSGRCh37
Celera1374,728,104 - 74,728,218UniSTS
HuRef1374,476,756 - 74,476,870UniSTS
D13S184E  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map13q32UniSTS
D13S184E  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map13q32UniSTS
D13S1665  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map13q32UniSTS
TNG Radiation Hybrid Map1333995.0UniSTS
GeneMap99-G3 RH Map132990.0UniSTS
D13S281  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map13q32UniSTS
TNG Radiation Hybrid Map1333714.0UniSTS
Stanford-G3 RH Map132677.0UniSTS
NCBI RH Map13867.7UniSTS
GeneMap99-G3 RH Map132976.0UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2346 2788 2228 4960 1724 2319 3 623 1276 463 2262 6571 5805 46 3729 1 844 1704 1586 170 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_011880 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521044 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017020298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017020299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017020300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017020301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017020302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047429990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054373972 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF105267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF111178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304338 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL137144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL138700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL139798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL160036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL160159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL161426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL162455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL354762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL354811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL356598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL357275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL450425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL606810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY358462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC106947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ009005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ182216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX640888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA267422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000377047   ⟹   ENSP00000366246
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1393,226,807 - 94,408,020 (+)Ensembl
Ensembl Acc Id: ENST00000617456   ⟹   ENSP00000477667
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1394,286,348 - 94,403,217 (+)Ensembl
RefSeq Acc Id: NM_005708   ⟹   NP_005699
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381393,226,807 - 94,408,020 (+)NCBI
GRCh371393,879,078 - 95,060,274 (+)RGD
GRCh371393,879,078 - 95,060,274 (+)NCBI
Build 361392,677,096 - 93,853,948 (+)NCBI Archive
Celera1374,727,460 - 75,908,516 (+)RGD
HuRef1374,476,112 - 75,657,237 (+)ENTREZGENE
CHM1_11393,848,682 - 95,029,827 (+)NCBI
T2T-CHM13v2.01392,430,763 - 93,611,616 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017020300   ⟹   XP_016875789
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381393,507,724 - 94,408,020 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017020302   ⟹   XP_016875791
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381394,114,123 - 94,408,020 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047429990   ⟹   XP_047285946
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381393,216,529 - 94,408,020 (+)NCBI
RefSeq Acc Id: XM_054373972   ⟹   XP_054229947
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01393,317,851 - 93,611,616 (+)NCBI
RefSeq Acc Id: NP_005699   ⟸   NM_005708
- Peptide Label: precursor
- UniProtKB: Q96SG8 (UniProtKB/Swiss-Prot),   Q96SG5 (UniProtKB/Swiss-Prot),   A8K279 (UniProtKB/Swiss-Prot),   Q9H1P4 (UniProtKB/Swiss-Prot),   Q9Y625 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016875789   ⟸   XM_017020300
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016875791   ⟸   XM_017020302
- Peptide Label: isoform X2
- Sequence:
Ensembl Acc Id: ENSP00000366246   ⟸   ENST00000377047
Ensembl Acc Id: ENSP00000477667   ⟸   ENST00000617456
RefSeq Acc Id: XP_047285946   ⟸   XM_047429990
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054229947   ⟸   XM_054373972
- Peptide Label: isoform X2

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y625-F1-model_v2 AlphaFold Q9Y625 1-555 view protein structure

Promoters
RGD ID:7226645
Promoter ID:EPDNEW_H19068
Type:initiation region
Name:GPC6_3
Description:glypican 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19069  EPDNEW_H19070  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381393,226,511 - 93,226,571EPDNEW
RGD ID:7226647
Promoter ID:EPDNEW_H19069
Type:initiation region
Name:GPC6_1
Description:glypican 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19068  EPDNEW_H19070  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381393,226,808 - 93,226,868EPDNEW
RGD ID:7226649
Promoter ID:EPDNEW_H19070
Type:initiation region
Name:GPC6_2
Description:glypican 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19068  EPDNEW_H19069  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381393,227,331 - 93,227,391EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:4454 AgrOrtholog
COSMIC GPC6 COSMIC
Ensembl Genes ENSG00000183098 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000377047 ENTREZGENE
  ENST00000377047.9 UniProtKB/Swiss-Prot
GTEx ENSG00000183098 GTEx
HGNC ID HGNC:4454 ENTREZGENE
Human Proteome Map GPC6 Human Proteome Map
InterPro Glypican UniProtKB/Swiss-Prot
  Glypican_CS UniProtKB/Swiss-Prot
KEGG Report hsa:10082 UniProtKB/Swiss-Prot
NCBI Gene 10082 ENTREZGENE
OMIM 604404 OMIM
PANTHER PTHR10822 UniProtKB/Swiss-Prot
  PTHR10822:SF31 UniProtKB/Swiss-Prot
Pfam Glypican UniProtKB/Swiss-Prot
PharmGKB PA28835 PharmGKB
PROSITE GLYPICAN UniProtKB/Swiss-Prot
UniProt A8K279 ENTREZGENE
  GPC6_HUMAN UniProtKB/Swiss-Prot
  Q96SG5 ENTREZGENE
  Q96SG8 ENTREZGENE
  Q9H1P4 ENTREZGENE
  Q9Y625 ENTREZGENE
UniProt Secondary A8K279 UniProtKB/Swiss-Prot
  Q96SG5 UniProtKB/Swiss-Prot
  Q96SG8 UniProtKB/Swiss-Prot
  Q9H1P4 UniProtKB/Swiss-Prot