GPC5 (glypican 5) - Rat Genome Database

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Gene: GPC5 (glypican 5) Homo sapiens
Analyze
Symbol: GPC5
Name: glypican 5
RGD ID: 1318835
HGNC Page HGNC:4453
Description: Predicted to be involved in cell migration; positive regulation of canonical Wnt signaling pathway; and regulation of protein localization to membrane. Predicted to be located in several cellular components, including Golgi lumen; extracellular region; and lysosomal lumen. Predicted to be active in cell surface.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: bA93M14.1; glypican proteoglycan 5; glypican-5
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Black 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
GRCh381391,398,621 - 92,867,237 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1391,398,621 - 92,873,682 (+)Ensemblhg38GRCh38
GRCh371392,050,875 - 93,519,490 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361390,848,930 - 92,317,491 (+)NCBIBuild 36Build 36hg18NCBI36
Build 341390,848,887 - 92,317,486NCBI
Celera1372,897,866 - 74,366,737 (+)NCBICelera
Cytogenetic Map13q31.3NCBI
HuRef1372,646,702 - 74,116,008 (+)NCBIHuRef
CHM1_11392,019,541 - 93,489,120 (+)NCBICHM1_1
T2T-CHM13v2.01390,601,154 - 92,070,908 (+)NCBIT2T-CHM13v2.0
JBrowse:




Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. 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:9070915   PMID:9331333   PMID:11292377   PMID:11566272   PMID:12477932   PMID:12721791   PMID:15057823   PMID:15489334   PMID:16344560   PMID:17846126   PMID:18195134  
PMID:19010793   PMID:19022413   PMID:19043545   PMID:19174780   PMID:19422935   PMID:19556317   PMID:19590514   PMID:19834535   PMID:19865102   PMID:20189936   PMID:20205591   PMID:20304703  
PMID:20360068   PMID:20360844   PMID:20379614   PMID:20688270   PMID:20692050   PMID:20881960   PMID:20886065   PMID:20944657   PMID:20966902   PMID:21339334   PMID:21441931   PMID:21873635  
PMID:21988832   PMID:22236185   PMID:23223018   PMID:23251661   PMID:23297363   PMID:23648065   PMID:23867465   PMID:23962560   PMID:24130709   PMID:24135429   PMID:24456789   PMID:24682381  
PMID:24943672   PMID:25189868   PMID:25429064   PMID:25818666   PMID:25999661   PMID:26631038   PMID:27157618   PMID:27465491   PMID:27554041   PMID:27806326   PMID:28893348   PMID:29407175  
PMID:30282023   PMID:30557546   PMID:30951720   PMID:32814053   PMID:33512817   PMID:33606708   PMID:33961781   PMID:34079082   PMID:35512704   PMID:39499777  


Genomics

Comparative Map Data
GPC5
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381391,398,621 - 92,867,237 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1391,398,621 - 92,873,682 (+)Ensemblhg38GRCh38
GRCh371392,050,875 - 93,519,490 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361390,848,930 - 92,317,491 (+)NCBIBuild 36Build 36hg18NCBI36
Build 341390,848,887 - 92,317,486NCBI
Celera1372,897,866 - 74,366,737 (+)NCBICelera
Cytogenetic Map13q31.3NCBI
HuRef1372,646,702 - 74,116,008 (+)NCBIHuRef
CHM1_11392,019,541 - 93,489,120 (+)NCBICHM1_1
T2T-CHM13v2.01390,601,154 - 92,070,908 (+)NCBIT2T-CHM13v2.0
Gpc5
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3914115,329,640 - 116,762,604 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl14115,329,647 - 116,762,591 (+)EnsemblGRCm39 EnsemblGRCm39
GRCm3814115,092,201 - 116,525,192 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl14115,092,215 - 116,525,179 (+)Ensemblmm10GRCm38
MGSCv3714115,491,437 - 116,924,414 (+)NCBIMGSCv37MGSCv37mm9NCBIm37
MGSCv3614113,974,089 - 115,406,638 (+)NCBIMGSCv36mm8
Celera14113,683,044 - 115,103,380 (+)NCBICelera
Cytogenetic Map14E4NCBI
cM Map1459.43NCBI
Gpc5
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81598,614,499 - 100,051,285 (+)NCBIGRCr8GRCr8GRCr8
GRCr8 Ensembl1598,646,340 - 100,051,514 (+)EnsemblGRCr8
mRatBN7.21592,207,275 - 93,644,054 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1592,239,176 - 93,643,282 (+)EnsemblmRatBN7.2
UTH_Rnor_SHR_Utx1596,146,021 - 97,550,277 (+)NCBIUTH_Rnor_SHR_UtxUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01597,278,871 - 98,683,154 (+)NCBIUTH_Rnor_SHRSP_BbbUtx_1.0UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01594,186,346 - 95,610,977 (+)NCBIUTH_Rnor_WKY_Bbb_1.0UTH_Rnor_WKY_Bbb_1.0
Rnor_6.015100,283,131 - 101,776,838 (+)NCBIRnor_6.0Rnor_6.0rn6Rnor6.0
Rnor_5.015103,739,948 - 104,456,749 (+)NCBIRnor_5.0Rnor_5.0rn5
Rnor_5.015105,221,065 - 105,224,752 (+)NCBIRnor_5.0Rnor_5.0rn5
RGSC_v3.41599,917,274 - 101,353,034 (+)NCBIRGSC_v3.4RGSC_v3.4rn4
Celera1591,103,971 - 92,504,072 (+)NCBICelera
RGSC_v3.11599,932,834 - 100,716,974 (+)NCBI
Cytogenetic Map15q23-q24NCBI
Gpc5
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540416,827,833 - 18,091,256 (-)Ensembl
ChiLan1.0NW_00495540416,824,366 - 18,091,464 (-)NCBIChiLan1.0ChiLan1.0
GPC5
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21492,946,967 - 94,407,470 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11391,613,624 - 92,365,064 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01372,588,968 - 74,051,961 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11391,755,264 - 93,206,407 (+)NCBIPanPan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1391,755,623 - 93,205,610 (+)EnsemblpanPan2panpan1.1
GPC5
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12242,526,426 - 43,873,992 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2242,526,054 - 43,870,405 (+)EnsemblcanFam3CanFam3.1
Dog10K_Boxer_Tasha2242,382,134 - 43,727,661 (+)NCBIDog10K_Boxer_TashaDog10K_Boxer_Tasha
ROS_Cfam_1.02242,927,701 - 44,302,647 (+)NCBIROS_Cfam_1.0ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2242,927,696 - 44,299,055 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12242,610,360 - 43,958,749 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02242,664,714 - 43,999,944 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02242,665,638 - 44,009,293 (+)NCBIUU_Cfam_GSD_1.0UU_Cfam_GSD_1.0
Gpc5
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404945178,229,811 - 178,459,961 (+)NCBIHiC_Itri_2
SpeTri2.0NW_00493647217,492,183 - 17,708,067 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
GPC5
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1160,791,363 - 62,147,239 (+)EnsemblsusScr11Sscrofa11.1
Sscrofa11.11160,791,000 - 62,149,911 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21166,666,602 - 67,323,189 (+)NCBISscrofa10.2Sscrofa10.2susScr3
GPC5
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1370,294,405 - 71,729,729 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604626,678,549 - 28,148,799 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Gpc5
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624779982,179 - 1,659,418 (-)EnsemblHetGla_female_1.0 EnsemblhetGla2HetGla_female_1.0 Ensembl
HetGla 1.0NW_004624779982,178 - 1,712,772 (-)NCBIHetGla 1.0HetGla 1.0hetGla2
Gpc5
(Rattus rattus - black rat)
Black Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rrattus_CSIRO_v11210,263,357 - 10,728,375 (-)NCBIRrattus_CSIRO_v1

Variants

.
Variants in GPC5
191 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_004466.5(GPC5):c.325+33247G>A single nucleotide variant Lung cancer [RCV000098418] Chr13:91482169 [GRCh38]
Chr13:92134423 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.325+45030C>A single nucleotide variant Lung cancer [RCV000098419] Chr13:91493952 [GRCh38]
Chr13:92146206 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.325+64107G>A single nucleotide variant Lung cancer [RCV000098420] Chr13:91513029 [GRCh38]
Chr13:92165283 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.325+84728A>T single nucleotide variant Lung cancer [RCV000098421] Chr13:91533650 [GRCh38]
Chr13:92185904 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.325+110538A>G single nucleotide variant Lung cancer [RCV000098422] Chr13:91559460 [GRCh38]
Chr13:92211714 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.326-40943C>A single nucleotide variant Lung cancer [RCV000098423] Chr13:91652244 [GRCh38]
Chr13:92304498 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.326-29501A>T single nucleotide variant Lung cancer [RCV000098424] Chr13:91663686 [GRCh38]
Chr13:92315940 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.326-25432A>G single nucleotide variant Lung cancer [RCV000098425] Chr13:91667755 [GRCh38]
Chr13:92320009 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.326-16040T>C single nucleotide variant Lung cancer [RCV000098426] Chr13:91677147 [GRCh38]
Chr13:92329401 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.326-12595T>C single nucleotide variant Lung cancer [RCV000098427] Chr13:91680592 [GRCh38]
Chr13:92332846 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1021-4944C>T single nucleotide variant Lung cancer [RCV000098428] Chr13:91723588 [GRCh38]
Chr13:92375842 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1155-7627T>A single nucleotide variant Lung cancer [RCV000098429] Chr13:91748668 [GRCh38]
Chr13:92400922 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1280+2661T>C single nucleotide variant Lung cancer [RCV000098430] Chr13:91759081 [GRCh38]
Chr13:92411335 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1280+7993C>A single nucleotide variant Lung cancer [RCV000098431] Chr13:91764413 [GRCh38]
Chr13:92416667 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1280+16190A>C single nucleotide variant Lung cancer [RCV000098432] Chr13:91772610 [GRCh38]
Chr13:92424864 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1280+22246C>A single nucleotide variant Lung cancer [RCV000098433] Chr13:91778666 [GRCh38]
Chr13:92430920 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1280+23974T>A single nucleotide variant Lung cancer [RCV000098434] Chr13:91780394 [GRCh38]
Chr13:92432648 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1281-19364G>T single nucleotide variant Lung cancer [RCV000098435] Chr13:91888573 [GRCh38]
Chr13:92540827 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1401+6932T>C single nucleotide variant Lung cancer [RCV000098436] Chr13:91914989 [GRCh38]
Chr13:92567243 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1401+97963C>G single nucleotide variant Lung cancer [RCV000098437] Chr13:92006021 [GRCh38]
Chr13:92658274 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1402-92806C>A single nucleotide variant Lung cancer [RCV000098438] Chr13:92052024 [GRCh38]
Chr13:92704277 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1402-65867G>T single nucleotide variant Lung cancer [RCV000098439] Chr13:92078963 [GRCh38]
Chr13:92731216 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1402-41618G>A single nucleotide variant Lung cancer [RCV000098440] Chr13:92103212 [GRCh38]
Chr13:92755465 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1402-2422G>C single nucleotide variant Lung cancer [RCV000098441] Chr13:92142408 [GRCh38]
Chr13:92794661 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+7157C>A single nucleotide variant Lung cancer [RCV000098442] Chr13:92152146 [GRCh38]
Chr13:92804399 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+25336A>G single nucleotide variant Lung cancer [RCV000098443] Chr13:92170325 [GRCh38]
Chr13:92822578 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+127097G>T single nucleotide variant Lung cancer [RCV000098444] Chr13:92272086 [GRCh38]
Chr13:92924339 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+140012T>A single nucleotide variant Lung cancer [RCV000098445] Chr13:92285001 [GRCh38]
Chr13:92937254 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+151505A>T single nucleotide variant Lung cancer [RCV000098446] Chr13:92296494 [GRCh38]
Chr13:92948747 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+180965T>A single nucleotide variant Lung cancer [RCV000098447] Chr13:92325954 [GRCh38]
Chr13:92978207 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+265246C>T single nucleotide variant Lung cancer [RCV000098448] Chr13:92410235 [GRCh38]
Chr13:93062488 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+271552C>A single nucleotide variant Lung cancer [RCV000098449] Chr13:92416541 [GRCh38]
Chr13:93068794 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+301052C>A single nucleotide variant Lung cancer [RCV000098450] Chr13:92446041 [GRCh38]
Chr13:93098294 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1561+339362A>C single nucleotide variant Lung cancer [RCV000098451] Chr13:92484351 [GRCh38]
Chr13:93136604 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1562-185694G>A single nucleotide variant Lung cancer [RCV000098452] Chr13:92680588 [GRCh38]
Chr13:93332841 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1562-95744T>A single nucleotide variant Lung cancer [RCV000098453] Chr13:92770538 [GRCh38]
Chr13:93422791 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1562-8084G>T single nucleotide variant Lung cancer [RCV000098454] Chr13:92858198 [GRCh38]
Chr13:93510451 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.5(GPC5):c.1562-2496C>T single nucleotide variant Lung cancer [RCV000098455] Chr13:92863786 [GRCh38]
Chr13:93516039 [GRCh37]
Chr13:13q31.3		 uncertain significance
GRCh38/hg38 13q14.12-31.3(chr13:44967523-92738168)x1 copy number loss See cases [RCV000050891] Chr13:44967523..92738168 [GRCh38]
Chr13:45541658..93390421 [GRCh37]
Chr13:44439658..92188422 [NCBI36]
Chr13:13q14.12-31.3		 pathogenic
GRCh38/hg38 13q31.3(chr13:91615056-91879009)x1 copy number loss See cases [RCV000050633] Chr13:91615056..91879009 [GRCh38]
Chr13:92267310..92531263 [GRCh37]
Chr13:91065311..91329264 [NCBI36]
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 13q31.1-34(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 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 13q31.1-33.2(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(chr13:90973752-93097331)x1 copy number loss See cases [RCV000051922] Chr13:90973752..93097331 [GRCh38]
Chr13:91626006..93749584 [GRCh37]
Chr13:90424007..92547585 [NCBI36]
Chr13:13q31.3		 uncertain significance
GRCh38/hg38 13q31.3(chr13:91431897-91628212)x1 copy number loss See cases [RCV000051923] Chr13:91431897..91628212 [GRCh38]
Chr13:92084151..92280466 [GRCh37]
Chr13:90882152..91078467 [NCBI36]
Chr13:13q31.3		 uncertain significance
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 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
NM_004466.5(GPC5):c.1710G>A (p.Gly570=) single nucleotide variant Malignant melanoma [RCV000070408] Chr13:92866430 [GRCh38]
Chr13:93518683 [GRCh37]
Chr13:92316684 [NCBI36]
Chr13:13q31.3		 not provided
NM_004466.5(GPC5):c.598G>A (p.Asp200Asn) single nucleotide variant Malignant melanoma [RCV000062699] Chr13:91693459 [GRCh38]
Chr13:92345713 [GRCh37]
Chr13:91143714 [NCBI36]
Chr13:13q31.3		 not provided
NM_004466.5(GPC5):c.1325G>A (p.Gly442Glu) single nucleotide variant Malignant melanoma [RCV000062700] Chr13:91907981 [GRCh38]
Chr13:92560235 [GRCh37]
Chr13:91358236 [NCBI36]
Chr13:13q31.3		 not provided
GRCh37/hg19 13q31.3(chr13:90644219-92557099)x1 copy number loss See cases [RCV000234861] Chr13:90644219..92557099 [GRCh37]
Chr13:13q31.3		 pathogenic
GRCh38/hg38 13q31.3(chr13:91521052-91597567)x1 copy number loss See cases [RCV000134626] Chr13:91521052..91597567 [GRCh38]
Chr13:92173306..92249821 [GRCh37]
Chr13:90971307..91047822 [NCBI36]
Chr13:13q31.3		 benign|likely benign|conflicting data from submitters
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 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
GRCh38/hg38 13q31.3(chr13:91413206-91615256)x1 copy number loss See cases [RCV000135429] Chr13:91413206..91615256 [GRCh38]
Chr13:92065460..92267510 [GRCh37]
Chr13:90863461..91065511 [NCBI36]
Chr13:13q31.3		 benign
GRCh38/hg38 13q22.3-31.3(chr13:77061780-92460406)x1 copy number loss See cases [RCV000136886] Chr13:77061780..92460406 [GRCh38]
Chr13:77635915..93112659 [GRCh37]
Chr13:76533916..91910660 [NCBI36]
Chr13:13q22.3-31.3		 pathogenic
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 13q31.1-31.3(chr13:84005264-92784013)x1 copy number loss See cases [RCV000137272] Chr13:84005264..92784013 [GRCh38]
Chr13:84579399..93436266 [GRCh37]
Chr13:83477400..92234267 [NCBI36]
Chr13:13q31.1-31.3		 likely 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 13q31.1-34(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 13q31.3(chr13:91896856-91922860)x1 copy number loss See cases [RCV000139292] Chr13:91896856..91922860 [GRCh38]
Chr13:92549110..92575114 [GRCh37]
Chr13:91347111..91373115 [NCBI36]
Chr13:13q31.3		 likely benign
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(chr13:92270151-92288777)x1 copy number loss See cases [RCV000139153] Chr13:92270151..92288777 [GRCh38]
Chr13:92922404..92941030 [GRCh37]
Chr13:91720405..91739031 [NCBI36]
Chr13:13q31.3		 likely benign
GRCh38/hg38 13q31.3(chr13:91413406-91625217)x1 copy number loss See cases [RCV000140000] Chr13:91413406..91625217 [GRCh38]
Chr13:92065660..92277471 [GRCh37]
Chr13:90863661..91075472 [NCBI36]
Chr13:13q31.3		 likely 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 13q31.3(chr13:91441741-91625217)x1 copy number loss See cases [RCV000141160] Chr13:91441741..91625217 [GRCh38]
Chr13:92093995..92277471 [GRCh37]
Chr13:90891996..91075472 [NCBI36]
Chr13:13q31.3		 likely benign
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 13q31.1-31.3(chr13:84052824-91838339)x3 copy number gain See cases [RCV000141994] Chr13:84052824..91838339 [GRCh38]
Chr13:84626959..92490593 [GRCh37]
Chr13:83524960..91288594 [NCBI36]
Chr13:13q31.1-31.3		 uncertain significance
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 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 13q31.3(chr13:91413406-91615115)x1 copy number loss See cases [RCV000142566] Chr13:91413406..91615115 [GRCh38]
Chr13:92065660..92267369 [GRCh37]
Chr13:90863661..91065370 [NCBI36]
Chr13:13q31.3		 uncertain significance|conflicting data from submitters
GRCh38/hg38 13q31.3(chr13:91799693-92057976)x1 copy number loss See cases [RCV000143545] Chr13:91799693..92057976 [GRCh38]
Chr13:92451947..92710229 [GRCh37]
Chr13:91249948..91508230 [NCBI36]
Chr13:13q31.3		 uncertain significance
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
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 13q12.11-34(chr13:19571503-115092569)x3 copy number gain See cases [RCV000240150] Chr13:19571503..115092569 [GRCh37]
Chr13:13q12.11-34		 pathogenic
GRCh37/hg19 13q31.3(chr13:92520462-92715040)x1 copy number loss See cases [RCV000207443] Chr13:92520462..92715040 [GRCh37]
Chr13:13q31.3		 likely benign
GRCh37/hg19 13q31.3(chr13:91209639-94704856)x3 copy number gain See cases [RCV000240035] Chr13:91209639..94704856 [GRCh37]
Chr13:13q31.3		 uncertain significance
GRCh37/hg19 13q31.3(chr13:93377562-93606814)x1 copy number loss VATER association [RCV000523902] Chr13:93377562..93606814 [GRCh37]
Chr13:13q31.3		 likely benign
GRCh37/hg19 13q22.1-31.3(chr13:74459395-93481294)x1 copy number loss See cases [RCV000598789] Chr13:74459395..93481294 [GRCh37]
Chr13:13q22.1-31.3		 pathogenic
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 13q31.3(chr13:92065660-92299019)x1 copy number loss not specified [RCV000452885] Chr13:92065660..92299019 [GRCh37]
Chr13:13q31.3		 uncertain significance
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(chr13:92062055-92303438)x1 copy number loss See cases [RCV000446126] Chr13:92062055..92303438 [GRCh37]
Chr13:13q31.3		 uncertain significance
GRCh37/hg19 13q31.3(chr13:92719735-92817257)x1 copy number loss See cases [RCV000447240] Chr13:92719735..92817257 [GRCh37]
Chr13:13q31.3		 likely benign
GRCh37/hg19 13q31.1-31.3(chr13:86963003-93390362)x3 copy number gain See cases [RCV000446248] Chr13:86963003..93390362 [GRCh37]
Chr13:13q31.1-31.3		 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 13q31.3(chr13:92979291-93049171) copy number gain Abnormal esophagus morphology [RCV000416646] Chr13:92979291..93049171 [GRCh37]
Chr13:13q31.3		 likely benign
GRCh37/hg19 13q31.3(chr13:92958981-93035128) copy number gain Abnormal esophagus morphology [RCV000416836] Chr13:92958981..93035128 [GRCh37]
Chr13:13q31.3		 likely benign
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 13q11-34(chr13:19436287-115107733) copy number gain See cases [RCV000510405] Chr13:19436287..115107733 [GRCh37]
Chr13:13q11-34		 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(chr13:92062055-92303438)x1 copy number loss See cases [RCV000510610] Chr13:92062055..92303438 [GRCh37]
Chr13:13q31.3		 conflicting data from submitters
GRCh37/hg19 13q31.3(chr13:92788368-92846125)x1 copy number loss See cases [RCV000511636] Chr13:92788368..92846125 [GRCh37]
Chr13:13q31.3		 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 13q31.1-33.3(chr13:80572498-108719528)x1 copy number loss See cases [RCV000510890] Chr13:80572498..108719528 [GRCh37]
Chr13:13q31.1-33.3		 pathogenic
NM_004466.6(GPC5):c.881C>T (p.Ala294Val) single nucleotide variant not specified [RCV004307037] Chr13:91693742 [GRCh38]
Chr13:92345996 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.239C>T (p.Ala80Val) single nucleotide variant not specified [RCV004289869] Chr13:91448836 [GRCh38]
Chr13:92101090 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.994C>G (p.Leu332Val) single nucleotide variant not specified [RCV004282270] Chr13:91693855 [GRCh38]
Chr13:92346109 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.20C>G (p.Pro7Arg) single nucleotide variant not specified [RCV004311347] Chr13:91399066 [GRCh38]
Chr13:92051320 [GRCh37]
Chr13:13q31.3		 likely benign
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 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(chr13:92432522-92646309)x1 copy number loss not provided [RCV000683501] Chr13:92432522..92646309 [GRCh37]
Chr13:13q31.3		 uncertain significance
GRCh37/hg19 13q31.3(chr13:92148518-93073022)x3 copy number gain not provided [RCV000683539] Chr13:92148518..93073022 [GRCh37]
Chr13:13q31.3		 likely benign
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 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 13q31.1-31.3(chr13:85005334-92461147)x1 copy number loss not provided [RCV000738268] Chr13:85005334..92461147 [GRCh37]
Chr13:13q31.1-31.3		 pathogenic
GRCh37/hg19 13q31.3(chr13:92209916-92255167)x3 copy number gain not provided [RCV000738286] Chr13:92209916..92255167 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92297112-92335293)x1 copy number loss not provided [RCV000738287] Chr13:92297112..92335293 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92302631-92303608)x4 copy number gain not provided [RCV000738288] Chr13:92302631..92303608 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92338197-92343219)x4 copy number gain not provided [RCV000738289] Chr13:92338197..92343219 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92880932-92921577)x3 copy number gain not provided [RCV000738290] Chr13:92880932..92921577 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92903538-92921577)x3 copy number gain not provided [RCV000738291] Chr13:92903538..92921577 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92904552-92921577)x4 copy number gain not provided [RCV000738292] Chr13:92904552..92921577 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92939212-92942044)x3 copy number gain not provided [RCV000738293] Chr13:92939212..92942044 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93009305-93018797)x1 copy number loss not provided [RCV000738294] Chr13:93009305..93018797 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93009537-93018797)x1 copy number loss not provided [RCV000738295] Chr13:93009537..93018797 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93009537-93020885)x1 copy number loss not provided [RCV000738296] Chr13:93009537..93020885 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93009816-93018797)x0 copy number loss not provided [RCV000738297] Chr13:93009816..93018797 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93009816-93018949)x1 copy number loss not provided [RCV000738298] Chr13:93009816..93018949 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93010082-93018797)x1 copy number loss not provided [RCV000738299] Chr13:93010082..93018797 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93011530-93015480)x1 copy number loss not provided [RCV000738300] Chr13:93011530..93015480 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93011563-93018797)x1 copy number loss not provided [RCV000738301] Chr13:93011563..93018797 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93013540-93015480)x1 copy number loss not provided [RCV000738302] Chr13:93013540..93015480 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93094243-93390360)x3 copy number gain not provided [RCV000738303] Chr13:93094243..93390360 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93175462-93289419)x3 copy number gain not provided [RCV000738304] Chr13:93175462..93289419 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93175462-93324938)x3 copy number gain not provided [RCV000738305] Chr13:93175462..93324938 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93283410-93289419)x3 copy number gain not provided [RCV000738306] Chr13:93283410..93289419 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93283410-93337765)x3 copy number gain not provided [RCV000738307] Chr13:93283410..93337765 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93284288-93327850)x3 copy number gain not provided [RCV000738308] Chr13:93284288..93327850 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93284647-93323495)x3 copy number gain not provided [RCV000738309] Chr13:93284647..93323495 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296244-93318965)x3 copy number gain not provided [RCV000738310] Chr13:93296244..93318965 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296337-93303777)x3 copy number gain not provided [RCV000738311] Chr13:93296337..93303777 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296337-93318965)x3 copy number gain not provided [RCV000738312] Chr13:93296337..93318965 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296337-93319209)x3 copy number gain not provided [RCV000738313] Chr13:93296337..93319209 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296337-93319383)x3 copy number gain not provided [RCV000738314] Chr13:93296337..93319383 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296337-93324938)x3 copy number gain not provided [RCV000738315] Chr13:93296337..93324938 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296337-93327734)x3 copy number gain not provided [RCV000738316] Chr13:93296337..93327734 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296337-93344385)x3 copy number gain not provided [RCV000738317] Chr13:93296337..93344385 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296337-93858612)x3 copy number gain not provided [RCV000738318] Chr13:93296337..93858612 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296384-93324938)x3 copy number gain not provided [RCV000738319] Chr13:93296384..93324938 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93297295-93319383)x3 copy number gain not provided [RCV000738320] Chr13:93297295..93319383 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93297295-93321101)x3 copy number gain not provided [RCV000738321] Chr13:93297295..93321101 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93351223-93412846)x3 copy number gain not provided [RCV000738322] Chr13:93351223..93412846 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93352874-93390360)x3 copy number gain not provided [RCV000738323] Chr13:93352874..93390360 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93352874-93415471)x3 copy number gain not provided [RCV000738324] Chr13:93352874..93415471 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93354092-93389909)x3 copy number gain not provided [RCV000738325] Chr13:93354092..93389909 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q11-34(chr13:19031237-115107157)x3 copy number gain not provided [RCV000750643] Chr13:19031237..115107157 [GRCh37]
Chr13:13q11-34		 pathogenic
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(chr13:92383193-92392002)x1 copy number loss not provided [RCV000750806] Chr13:92383193..92392002 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92387661-92392002)x1 copy number loss not provided [RCV000750807] Chr13:92387661..92392002 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92419769-92501699)x1 copy number loss not provided [RCV000750808] Chr13:92419769..92501699 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92432843-92815210)x3 copy number gain not provided [RCV000750809] Chr13:92432843..92815210 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92451453-92481564)x3 copy number gain not provided [RCV000750810] Chr13:92451453..92481564 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92451821-92921577)x3 copy number gain not provided [RCV000750811] Chr13:92451821..92921577 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92457521-92481564)x3 copy number gain not provided [RCV000750812] Chr13:92457521..92481564 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92458434-92481564)x3 copy number gain not provided [RCV000750813] Chr13:92458434..92481564 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92493999-92500759)x1 copy number loss not provided [RCV000750814] Chr13:92493999..92500759 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92564510-92619739)x3 copy number gain not provided [RCV000750815] Chr13:92564510..92619739 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92628841-92703934)x3 copy number gain not provided [RCV000750816] Chr13:92628841..92703934 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92718251-92723647)x4 copy number gain not provided [RCV000750817] Chr13:92718251..92723647 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92718700-92723725)x3 copy number gain not provided [RCV000750818] Chr13:92718700..92723725 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92834615-92840904)x3 copy number gain not provided [RCV000750819] Chr13:92834615..92840904 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92877891-92921577)x3 copy number gain not provided [RCV000750820] Chr13:92877891..92921577 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92880289-92921577)x3 copy number gain not provided [RCV000750821] Chr13:92880289..92921577 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93175462-93390360)x3 copy number gain not provided [RCV000750822] Chr13:93175462..93390360 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93175898-93390360)x3 copy number gain not provided [RCV000750823] Chr13:93175898..93390360 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93178967-93344385)x3 copy number gain not provided [RCV000750824] Chr13:93178967..93344385 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93200803-93390360)x3 copy number gain not provided [RCV000750825] Chr13:93200803..93390360 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93204608-93240822)x3 copy number gain not provided [RCV000750826] Chr13:93204608..93240822 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93208593-93241744)x3 copy number gain not provided [RCV000750827] Chr13:93208593..93241744 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93208593-93243648)x3 copy number gain not provided [RCV000750828] Chr13:93208593..93243648 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93232301-93240822)x4 copy number gain not provided [RCV000750829] Chr13:93232301..93240822 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93235051-93243648)x3 copy number gain not provided [RCV000750830] Chr13:93235051..93243648 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93244597-93245898)x0 copy number loss not provided [RCV000750831] Chr13:93244597..93245898 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93244802-93246790)x0 copy number loss not provided [RCV000750832] Chr13:93244802..93246790 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93244802-93269486)x0 copy number loss not provided [RCV000750833] Chr13:93244802..93269486 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93259449-93324938)x3 copy number gain not provided [RCV000750834] Chr13:93259449..93324938 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93262473-93390360)x3 copy number gain not provided [RCV000750835] Chr13:93262473..93390360 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93263813-93344385)x3 copy number gain not provided [RCV000750836] Chr13:93263813..93344385 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93282229-93337765)x3 copy number gain not provided [RCV000750837] Chr13:93282229..93337765 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93297295-93324938)x3 copy number gain not provided [RCV000750838] Chr13:93297295..93324938 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93298000-93302967)x4 copy number gain not provided [RCV000750839] Chr13:93298000..93302967 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93298000-93307119)x3 copy number gain not provided [RCV000750840] Chr13:93298000..93307119 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93298000-93324938)x3 copy number gain not provided [RCV000750841] Chr13:93298000..93324938 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93298036-93303000)x4 copy number gain not provided [RCV000750842] Chr13:93298036..93303000 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93302308-93318965)x3 copy number gain not provided [RCV000750843] Chr13:93302308..93318965 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93302308-93319209)x3 copy number gain not provided [RCV000750844] Chr13:93302308..93319209 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93303000-93337765)x3 copy number gain not provided [RCV000750845] Chr13:93303000..93337765 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93303107-93337765)x3 copy number gain not provided [RCV000750846] Chr13:93303107..93337765 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93304638-93318965)x3 copy number gain not provided [RCV000750847] Chr13:93304638..93318965 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93304638-93319254)x3 copy number gain not provided [RCV000750848] Chr13:93304638..93319254 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93304638-93319383)x3 copy number gain not provided [RCV000750849] Chr13:93304638..93319383 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93315329-93320347)x3 copy number gain not provided [RCV000750850] Chr13:93315329..93320347 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93315361-93412846)x3 copy number gain not provided [RCV000750851] Chr13:93315361..93412846 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93325820-93337765)x3 copy number gain not provided [RCV000750852] Chr13:93325820..93337765 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93325820-93344385)x3 copy number gain not provided [RCV000750853] Chr13:93325820..93344385 [GRCh37]
Chr13:13q31.3		 benign
NM_004466.6(GPC5):c.991C>T (p.His331Tyr) single nucleotide variant not provided [RCV000970882] Chr13:91693852 [GRCh38]
Chr13:92346106 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:93296466-93861493)x3 copy number gain not provided [RCV000849446] Chr13:93296466..93861493 [GRCh37]
Chr13:13q31.3		 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 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(chr13:92062330-92301985)x1 copy number loss not provided [RCV000848413] Chr13:92062330..92301985 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.153G>A (p.Ser51=) single nucleotide variant not provided [RCV000896029] Chr13:91399199 [GRCh38]
Chr13:92051453 [GRCh37]
Chr13:13q31.3		 benign
NM_004466.6(GPC5):c.483A>G (p.Glu161=) single nucleotide variant not provided [RCV000886619] Chr13:91693344 [GRCh38]
Chr13:92345598 [GRCh37]
Chr13:13q31.3		 benign
GRCh37/hg19 13q31.3(chr13:92531775-92614137)x1 copy number loss not provided [RCV001006585] Chr13:92531775..92614137 [GRCh37]
Chr13:13q31.3		 uncertain significance
GRCh37/hg19 13q31.3(chr13:92502204-92633877)x1 copy number loss not provided [RCV001006584] Chr13:92502204..92633877 [GRCh37]
Chr13:13q31.3		 uncertain significance
GRCh37/hg19 13q14.3-34(chr13:53262013-115107733)x1 copy number loss not provided [RCV001006567] Chr13:53262013..115107733 [GRCh37]
Chr13:13q14.3-34		 pathogenic
GRCh37/hg19 13q31.3(chr13:91460305-92069153)x3 copy number gain not provided [RCV001006582] Chr13:91460305..92069153 [GRCh37]
Chr13:13q31.3		 likely pathogenic
GRCh37/hg19 13q31.3(chr13:93496718-93752908)x3 copy number gain not provided [RCV001006586] Chr13:93496718..93752908 [GRCh37]
Chr13:13q31.3		 likely benign
GRCh37/hg19 13q31.3(chr13:92343338-92579579)x3 copy number gain not provided [RCV001006583] Chr13:92343338..92579579 [GRCh37]
Chr13:13q31.3		 uncertain significance
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(chr13:19053605-115108528)x3 copy number gain See cases [RCV001353184] Chr13:19053605..115108528 [GRCh37]
Chr13:13q11-34		 pathogenic
NC_000013.10:g.(?_92002837)_(103343314_?)del deletion Holoprosencephaly 5 [RCV001388033] Chr13:92002837..103343314 [GRCh37]
Chr13:13q31.3-33.1		 pathogenic
GRCh37/hg19 13q31.3(chr13:91284502-92325104)x1 copy number loss See cases [RCV002285045] Chr13:91284502..92325104 [GRCh37]
Chr13:13q31.3		 pathogenic
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 13q21.2-34(chr13:61424168-115107733) copy number gain not specified [RCV002053063] Chr13:61424168..115107733 [GRCh37]
Chr13:13q21.2-34		 pathogenic
GRCh37/hg19 13q31.1-34(chr13:85037147-115107733) copy number gain not specified [RCV002053073] Chr13:85037147..115107733 [GRCh37]
Chr13:13q31.1-34		 pathogenic
GRCh37/hg19 13q31.3(chr13:93296805-93862088)x3 copy number gain not provided [RCV001829085] Chr13:93296805..93862088 [GRCh37]
Chr13:13q31.3		 likely benign
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 13q11-34(chr13:19436286-115107733)x3 copy number gain not provided [RCV001834436] Chr13:19436286..115107733 [GRCh37]
Chr13:13q11-34		 pathogenic
GRCh37/hg19 13q31.3(chr13:92672250-92899251)x1 copy number loss not provided [RCV001829073] Chr13:92672250..92899251 [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 13q31.3(chr13:92062055-92303438) copy number loss not specified [RCV002053075] Chr13:92062055..92303438 [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
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
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 13q11-34(chr13:19253848-115108937)x3 copy number gain not provided [RCV002291540] Chr13:19253848..115108937 [GRCh37]
Chr13:13q11-34		 pathogenic
NM_004466.6(GPC5):c.1633A>G (p.Thr545Ala) single nucleotide variant not specified [RCV004327284] Chr13:92866353 [GRCh38]
Chr13:93518606 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.881C>G (p.Ala294Gly) single nucleotide variant not specified [RCV004161177] Chr13:91693742 [GRCh38]
Chr13:92345996 [GRCh37]
Chr13:13q31.3		 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 13q22.1-34(chr13:75268539-115107733)x3 copy number gain not provided [RCV002472537] Chr13:75268539..115107733 [GRCh37]
Chr13:13q22.1-34		 pathogenic
NM_004466.6(GPC5):c.899A>G (p.Glu300Gly) single nucleotide variant not specified [RCV004172785] Chr13:91693760 [GRCh38]
Chr13:92346014 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.311C>T (p.Ala104Val) single nucleotide variant not specified [RCV004210010] Chr13:91448908 [GRCh38]
Chr13:92101162 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.566A>G (p.Glu189Gly) single nucleotide variant not specified [RCV004234796] Chr13:91693427 [GRCh38]
Chr13:92345681 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.47T>C (p.Leu16Pro) single nucleotide variant not specified [RCV004088920] Chr13:91399093 [GRCh38]
Chr13:92051347 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.298A>G (p.Ile100Val) single nucleotide variant not specified [RCV004233262] Chr13:91448895 [GRCh38]
Chr13:92101149 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.520G>C (p.Val174Leu) single nucleotide variant not specified [RCV004128035] Chr13:91693381 [GRCh38]
Chr13:92345635 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1148G>A (p.Arg383Lys) single nucleotide variant not specified [RCV004152444] Chr13:91728659 [GRCh38]
Chr13:92380913 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.130G>A (p.Ala44Thr) single nucleotide variant not specified [RCV004174522] Chr13:91399176 [GRCh38]
Chr13:92051430 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1466G>A (p.Gly489Asp) single nucleotide variant not specified [RCV004125890] Chr13:92144894 [GRCh38]
Chr13:92797147 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1449G>T (p.Gln483His) single nucleotide variant not specified [RCV004124405] Chr13:92144877 [GRCh38]
Chr13:92797130 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.272C>T (p.Thr91Met) single nucleotide variant not specified [RCV004240846] Chr13:91448869 [GRCh38]
Chr13:92101123 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1451T>C (p.Leu484Pro) single nucleotide variant not specified [RCV004137453] Chr13:92144879 [GRCh38]
Chr13:92797132 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1591G>A (p.Val531Ile) single nucleotide variant not specified [RCV004088995] Chr13:92866311 [GRCh38]
Chr13:93518564 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.79G>A (p.Val27Met) single nucleotide variant not specified [RCV004092957] Chr13:91399125 [GRCh38]
Chr13:92051379 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.7G>A (p.Ala3Thr) single nucleotide variant not specified [RCV004088504] Chr13:91399053 [GRCh38]
Chr13:92051307 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1040G>A (p.Arg347His) single nucleotide variant not specified [RCV004211494] Chr13:91728551 [GRCh38]
Chr13:92380805 [GRCh37]
Chr13:13q31.3		 likely benign
NM_004466.6(GPC5):c.1151G>T (p.Arg384Ile) single nucleotide variant not specified [RCV004171967] Chr13:91728662 [GRCh38]
Chr13:92380916 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1663G>C (p.Glu555Gln) single nucleotide variant not specified [RCV004125684] Chr13:92866383 [GRCh38]
Chr13:93518636 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.584G>A (p.Arg195Gln) single nucleotide variant not provided [RCV004696402]|not specified [RCV004283743] Chr13:91693445 [GRCh38]
Chr13:92345699 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.283A>G (p.Thr95Ala) single nucleotide variant not specified [RCV004287303] Chr13:91448880 [GRCh38]
Chr13:92101134 [GRCh37]
Chr13:13q31.3		 likely benign
NM_004466.6(GPC5):c.1259A>T (p.Asn420Ile) single nucleotide variant not specified [RCV004275504] Chr13:91756399 [GRCh38]
Chr13:92408653 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1678A>G (p.Thr560Ala) single nucleotide variant not specified [RCV004274806] Chr13:92866398 [GRCh38]
Chr13:93518651 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.22G>T (p.Val8Leu) single nucleotide variant not specified [RCV004251209] Chr13:91399068 [GRCh38]
Chr13:92051322 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1670T>A (p.Met557Lys) single nucleotide variant not specified [RCV004296630] Chr13:92866390 [GRCh38]
Chr13:93518643 [GRCh37]
Chr13:13q31.3		 uncertain significance
GRCh38/hg38 13q31.3(chr13:91423419-91631346) copy number loss See cases [RCV003223554] Chr13:91423419..91631346 [GRCh38]
Chr13:13q31.3		 benign|uncertain significance
NM_004466.6(GPC5):c.1379A>G (p.Asp460Gly) single nucleotide variant not specified [RCV004355471] Chr13:91908035 [GRCh38]
Chr13:92560289 [GRCh37]
Chr13:13q31.3		 uncertain significance
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 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 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 13q31.1-34(chr13:84669397-115107733)x1 copy number loss not specified [RCV003987038] Chr13:84669397..115107733 [GRCh37]
Chr13:13q31.1-34		 pathogenic
GRCh37/hg19 13q21.1-31.3(chr13:56450978-93582180)x1 copy number loss not specified [RCV003987013] Chr13:56450978..93582180 [GRCh37]
Chr13:13q21.1-31.3		 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
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
GRCh37/hg19 13q31.3(chr13:92314605-92396512)x1 copy number loss not specified [RCV003987014] Chr13:92314605..92396512 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.776C>G (p.Pro259Arg) single nucleotide variant GPC5-related disorder [RCV003967144] Chr13:91693637 [GRCh38]
Chr13:92345891 [GRCh37]
Chr13:13q31.3		 likely benign
NM_004466.6(GPC5):c.730T>G (p.Phe244Val) single nucleotide variant GPC5-related disorder [RCV003929569] Chr13:91693591 [GRCh38]
Chr13:92345845 [GRCh37]
Chr13:13q31.3		 likely benign
NM_004466.6(GPC5):c.557G>T (p.Ser186Ile) single nucleotide variant GPC5-related disorder [RCV003944091] Chr13:91693418 [GRCh38]
Chr13:92345672 [GRCh37]
Chr13:13q31.3		 likely benign
NM_004466.6(GPC5):c.1679C>T (p.Thr560Ile) single nucleotide variant not specified [RCV004388115] Chr13:92866399 [GRCh38]
Chr13:93518652 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.67C>A (p.Arg23Ser) single nucleotide variant not specified [RCV004388117] Chr13:91399113 [GRCh38]
Chr13:92051367 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1637C>A (p.Thr546Lys) single nucleotide variant not specified [RCV004388114] Chr13:92866357 [GRCh38]
Chr13:93518610 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.989C>T (p.Ala330Val) single nucleotide variant not specified [RCV004388118] Chr13:91693850 [GRCh38]
Chr13:92346104 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.20C>A (p.Pro7His) single nucleotide variant not specified [RCV004388116] Chr13:91399066 [GRCh38]
Chr13:92051320 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1697T>A (p.Met566Lys) single nucleotide variant not specified [RCV004623969] Chr13:92866417 [GRCh38]
Chr13:93518670 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1592T>C (p.Val531Ala) single nucleotide variant not specified [RCV004623970] Chr13:92866312 [GRCh38]
Chr13:93518565 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1111A>T (p.Thr371Ser) single nucleotide variant not specified [RCV004632262] Chr13:91728622 [GRCh38]
Chr13:92380876 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.685C>T (p.Leu229Phe) single nucleotide variant not specified [RCV004632263] Chr13:91693546 [GRCh38]
Chr13:92345800 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1286C>T (p.Thr429Ile) single nucleotide variant not specified [RCV004632264] Chr13:91907942 [GRCh38]
Chr13:92560196 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1126A>G (p.Ser376Gly) single nucleotide variant not specified [RCV004632265] Chr13:91728637 [GRCh38]
Chr13:92380891 [GRCh37]
Chr13:13q31.3		 likely benign
NM_004466.6(GPC5):c.1611A>G (p.Thr537=) single nucleotide variant not provided [RCV004811385] Chr13:92866331 [GRCh38]
Chr13:93518584 [GRCh37]
Chr13:13q31.3		 likely benign
NM_004466.6(GPC5):c.836G>A (p.Arg279Gln) single nucleotide variant GPC5-related disorder [RCV004759227] Chr13:91693697 [GRCh38]
Chr13:92345951 [GRCh37]
Chr13:13q31.3		 uncertain significance
GRCh37/hg19 13q11-31.3(chr13:19436287-92292639)x3 copy number gain not provided [RCV004819310] Chr13:19436287..92292639 [GRCh37]
Chr13:13q11-31.3		 pathogenic
GRCh37/hg19 13q31.2-31.3(chr13:89945802-92671868)x1 copy number loss not provided [RCV004819857] Chr13:89945802..92671868 [GRCh37]
Chr13:13q31.2-31.3		 uncertain significance
NM_004466.6(GPC5):c.1070G>A (p.Arg357His) single nucleotide variant not specified [RCV004922209] Chr13:91728581 [GRCh38]
Chr13:92380835 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1311C>G (p.Ile437Met) single nucleotide variant not specified [RCV004932965] Chr13:91907967 [GRCh38]
Chr13:92560221 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.645G>A (p.Met215Ile) single nucleotide variant not specified [RCV004932966] Chr13:91693506 [GRCh38]
Chr13:92345760 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1114A>G (p.Thr372Ala) single nucleotide variant not specified [RCV005342756] Chr13:91728625 [GRCh38]
Chr13:92380879 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.601G>A (p.Val201Met) single nucleotide variant not specified [RCV005342757] Chr13:91693462 [GRCh38]
Chr13:92345716 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.136A>G (p.Arg46Gly) single nucleotide variant not specified [RCV005342754] Chr13:91399182 [GRCh38]
Chr13:92051436 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1067C>A (p.Pro356His) single nucleotide variant not specified [RCV005342755] Chr13:91728578 [GRCh38]
Chr13:92380832 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1706C>T (p.Pro569Leu) single nucleotide variant not specified [RCV005351175] Chr13:92866426 [GRCh38]
Chr13:93518679 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.542C>T (p.Pro181Leu) single nucleotide variant not specified [RCV005351176] Chr13:91693403 [GRCh38]
Chr13:92345657 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.836G>T (p.Arg279Leu) single nucleotide variant not specified [RCV005351177] Chr13:91693697 [GRCh38]
Chr13:92345951 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.812T>C (p.Met271Thr) single nucleotide variant not specified [RCV005351183] Chr13:91693673 [GRCh38]
Chr13:92345927 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1441C>G (p.Leu481Val) single nucleotide variant not specified [RCV005351178] Chr13:92144869 [GRCh38]
Chr13:92797122 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.401C>A (p.Ala134Asp) single nucleotide variant not specified [RCV005351179] Chr13:91693262 [GRCh38]
Chr13:92345516 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.456A>T (p.Leu152Phe) single nucleotide variant not specified [RCV005351180] Chr13:91693317 [GRCh38]
Chr13:92345571 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1144A>C (p.Asn382His) single nucleotide variant not specified [RCV005351182] Chr13:91728655 [GRCh38]
Chr13:92380909 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.602T>C (p.Val201Ala) single nucleotide variant not specified [RCV005351184] Chr13:91693463 [GRCh38]
Chr13:92345717 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.1661C>A (p.Thr554Asn) single nucleotide variant not specified [RCV004922211] Chr13:92866381 [GRCh38]
Chr13:93518634 [GRCh37]
Chr13:13q31.3		 uncertain significance
NM_004466.6(GPC5):c.158G>A (p.Arg53Gln) single nucleotide variant not specified [RCV004922210] Chr13:91399204 [GRCh38]
Chr13:92051458 [GRCh37]
Chr13:13q31.3		 uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:276
Count of miRNA genes:234
Interacting mature miRNAs:244
Transcripts:ENST00000377067, ENST00000483422
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597291417GWAS1387491_Hresponse to radiation, edema QTL GWAS1387491 (human)1e-09response to radiation, edema139228598392285984Human
597021589GWAS1117663_Hgrowth-regulated alpha protein measurement QTL GWAS1117663 (human)0.000006growth-regulated alpha protein measurement139249010992490110Human
628669817GWAS2578046_HTinnitus QTL GWAS2578046 (human)0.000001Tinnitus139238861392388614Human
597334425GWAS1430499_HAlzheimer disease, APOE carrier status QTL GWAS1430499 (human)0.000008Alzheimer disease, APOE carrier status139243907392439074Human
597152660GWAS1248734_Hlifestyle measurement, maximum cigarettes per day measurement QTL GWAS1248734 (human)0.0000001lifestyle measurement, maximum cigarettes per day measurement139265763892657639Human
407286339GWAS935315_Hvaginal microbiome measurement QTL GWAS935315 (human)0.000006vaginal microbiome measurement139170750191707502Human
407195215GWAS844191_Hcleft lip QTL GWAS844191 (human)0.000008cleft lip139269155592691556Human
597161369GWAS1257443_Halpha-tocopherol measurement QTL GWAS1257443 (human)0.000002alpha-tocopherol measurement139241317492413175Human
628751209GWAS2659438_Hresponse to radiation, edema QTL GWAS2659438 (human)1e-09response to radiation, edema139228598392285984Human
407180372GWAS829348_HFEV/FVC ratio QTL GWAS829348 (human)5e-10FEV/FVC ratio139178462291784623Human
628776299GWAS2684528_Hurate measurement, bone tissue density QTL GWAS2684528 (human)3e-13urate measurement, bone tissue densityblood uric acid level (CMO:0000501)139194444891944449Human
406906450GWAS555426_Hsmoking initiation QTL GWAS555426 (human)2e-09smoking initiation139239347092393471Human
597232525GWAS1328599_Hbiological sex QTL GWAS1328599 (human)2e-08biological sex139280846992808470Human
628767596GWAS2675825_Hblood protein amount QTL GWAS2675825 (human)2e-56blood protein amount139143138191431382Human
616494248GWAS1890831_Hquinate measurement QTL GWAS1890831 (human)0.000001quinate measurement139268290092682901Human
597232001GWAS1328075_Hself reported educational attainment QTL GWAS1328075 (human)4e-09self reported educational attainment139267896992678970Human
628850529GWAS2758758_Hsevere acute respiratory syndrome, COVID-19 QTL GWAS2758758 (human)2e-15severe acute respiratory syndrome, COVID-19139262951592629516Human
628796257GWAS2704486_Hprotein measurement QTL GWAS2704486 (human)1e-23protein amount (VT:0010120)139178517691785177Human
628861796GWAS2770025_H1,3,7-trimethylurate measurement QTL GWAS2770025 (human)0.0000011,3,7-trimethylurate measurement139154564091545641Human
628410731GWAS2318960_Hgut microbiome measurement QTL GWAS2318960 (human)0.000005gut microbiome measurement139190458091904581Human
617142504GWAS2160003_Hglypican-5 measurement QTL GWAS2160003 (human)4e-292glypican-5 measurement139141774491417745Human
407359591GWAS1008567_Hinsomnia QTL GWAS1008567 (human)4e-08insomnia139224525592245256Human
617142505GWAS2160004_Hglypican-5 measurement QTL GWAS2160004 (human)2e-16glypican-5 measurement139165302391653024Human
598141319GWAS1828047_Hpancreatic intraductal papillary-mucinous neoplasm QTL GWAS1828047 (human)0.000001pancreatic intraductal papillary-mucinous neoplasm139216806292168063Human
598110599GWAS1819482_Holigodendroglioma QTL GWAS1819482 (human)0.000005oligodendroglioma139258335592583356Human
617142506GWAS2160005_Hglypican-5 measurement QTL GWAS2160005 (human)1e-22glypican-5 measurement139184028591840286Human
617142507GWAS2160006_Hglypican-5 measurement QTL GWAS2160006 (human)5e-74glypican-5 measurement139178245191782452Human
617142508GWAS2160007_Hglypican-5 measurement QTL GWAS2160007 (human)8e-27glypican-5 measurement139164447691644477Human
616372889GWAS1853131_Hobsolete_blood protein measurement QTL GWAS1853131 (human)1e-10obsolete_blood protein measurement139202820592028206Human
617137900GWAS2155399_Hglypican-5 measurement QTL GWAS2155399 (human)9e-12glypican-5 measurement139214680092146801Human
407282786GWAS931762_Htaste liking measurement QTL GWAS931762 (human)1e-09taste liking measurement139278039392780394Human
617142509GWAS2160008_Hglypican-5 measurement QTL GWAS2160008 (human)1e-11glypican-5 measurement139140910591409106Human
617137901GWAS2155400_Hglypican-5 measurement QTL GWAS2155400 (human)2e-22glypican-5 measurement139163202491632025Human
616372888GWAS1853130_Hobsolete_blood protein measurement QTL GWAS1853130 (human)1e-36obsolete_blood protein measurement139179962991799630Human
407293027GWAS942003_Hbrain measurement QTL GWAS942003 (human)2e-08brain measurement139219971592199716Human
617142510GWAS2160009_Hglypican-5 measurement QTL GWAS2160009 (human)2e-23glypican-5 measurement139232047992320480Human
617137903GWAS2155402_Hglypican-5 measurement QTL GWAS2155402 (human)4e-66glypican-5 measurement139197475591974756Human
617142511GWAS2160010_Hglypican-5 measurement QTL GWAS2160010 (human)7e-13glypican-5 measurement139220437692204377Human
597219248GWAS1315322_Hbody height QTL GWAS1315322 (human)3e-10body height139213559192135592Human
407075947GWAS724923_Hrheumatoid arthritis QTL GWAS724923 (human)3e-09rheumatoid arthritis139229363192293632Human
617137912GWAS2155411_Hglypican-5 measurement QTL GWAS2155411 (human)8e-25glypican-5 measurement139168867591688676Human
617137913GWAS2155412_Hglypican-5 measurement QTL GWAS2155412 (human)1e-13glypican-5 measurement139182232291822323Human
597063076GWAS1159150_HBMI-adjusted waist circumference QTL GWAS1159150 (human)0.000003body size trait (VT:0100005)139190589091905891Human
617137914GWAS2155413_Hglypican-5 measurement QTL GWAS2155413 (human)3e-12glypican-5 measurement139220981092209811Human
407075953GWAS724929_Hrheumatoid arthritis QTL GWAS724929 (human)0.000003rheumatoid arthritis139229363192293632Human
597171628GWAS1267702_Hsex interaction measurement, longitudinal BMI measurement QTL GWAS1267702 (human)0.000001sex interaction measurement, longitudinal BMI measurement139215225392152254Human
617137917GWAS2155416_Hglypican-5 measurement QTL GWAS2155416 (human)6e-15glypican-5 measurement139223054692230547Human
617137918GWAS2155417_Hglypican-5 measurement QTL GWAS2155417 (human)8e-22glypican-5 measurement139206609892066099Human
617137919GWAS2155418_Hglypican-5 measurement QTL GWAS2155418 (human)6e-14glypican-5 measurement139153122491531225Human
617137904GWAS2155403_Hglypican-5 measurement QTL GWAS2155403 (human)2e-18glypican-5 measurement139156397891563979Human
617137906GWAS2155405_Hglypican-5 measurement QTL GWAS2155405 (human)6e-24glypican-5 measurement139183649691836497Human
628791105GWAS2699334_Hcervical cancer QTL GWAS2699334 (human)0.000003cervical cancer139161842391618424Human
628896071GWAS2804300_Hglypican-5 measurement QTL GWAS2804300 (human)6e-167glypican-5 measurement139176480491764805Human
407027326GWAS676302_Hlung carcinoma QTL GWAS676302 (human)0.000006lung integrity trait (VT:0010906)139179297591792976Human
617137910GWAS2155409_Hglypican-5 measurement QTL GWAS2155409 (human)3e-15glypican-5 measurement139183800391838004Human
616539391GWAS1935974_Hglypican-5 measurement QTL GWAS1935974 (human)3e-74glypican-5 measurement139186758291867583Human
407107587GWAS756563_Hgrowth-regulated alpha protein measurement QTL GWAS756563 (human)0.000006growth-regulated alpha protein measurement139249010992490110Human
616539390GWAS1935973_Hglypican-5 measurement QTL GWAS1935973 (human)1e-52glypican-5 measurement139192765191927652Human
616539389GWAS1935972_Hglypican-5 measurement QTL GWAS1935972 (human)7e-16glypican-5 measurement139243966992439670Human
616539388GWAS1935971_Hglypican-5 measurement QTL GWAS1935971 (human)6e-14glypican-5 measurement139153122491531225Human
616539387GWAS1935970_Hglypican-5 measurement QTL GWAS1935970 (human)8e-22glypican-5 measurement139206609892066099Human
406892549GWAS541525_Hglypican-5 measurement QTL GWAS541525 (human)5e-233glypican-5 measurement139177069291770693Human
616539386GWAS1935969_Hglypican-5 measurement QTL GWAS1935969 (human)4e-113glypican-5 measurement139205173292051733Human
628928826GWAS2837055_Hlung carcinoma QTL GWAS2837055 (human)0.0000002lung integrity trait (VT:0010906)139167394191673942Human
407179778GWAS828754_Hcolor vision disorder QTL GWAS828754 (human)0.000009color vision disorder139160933491609335Human
406971398GWAS620374_Hspine bone mineral density QTL GWAS620374 (human)0.000006bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)139189717091897171Human
407070724GWAS719700_Heducational attainment QTL GWAS719700 (human)0.0000001educational attainment139253965292539653Human
406980106GWAS629082_Hreading and spelling ability QTL GWAS629082 (human)0.000008reading and spelling ability139141682091416821Human
597266385GWAS1362459_Hglypican-5 measurement QTL GWAS1362459 (human)6e-167glypican-5 measurement139176480491764805Human
597389771GWAS1485845_HAstigmatism QTL GWAS1485845 (human)0.000008Astigmatism139250020592500206Human
597315016GWAS1411090_Hvaginal microbiome measurement QTL GWAS1411090 (human)0.000006vaginal microbiome measurement139170750191707502Human
628701487GWAS2609716_Hvaginal microbiome measurement QTL GWAS2609716 (human)0.000006vaginal microbiome measurement139170750191707502Human
597280718GWAS1376792_Hmemory performance, cognitive function measurement, major depressive disorder QTL GWAS1376792 (human)0.0000003memory performance, cognitive function measurement, major depressive disorder139226401592264016Human
406934556GWAS583532_Hblood protein measurement QTL GWAS583532 (human)2e-218blood protein measurement139177069291770693Human
406964259GWAS613235_HCOVID-19 QTL GWAS613235 (human)0.0000007COVID-19139144034491440345Human
597306367GWAS1402441_Hbrain measurement QTL GWAS1402441 (human)2e-08brain measurement139219971592199716Human
597036528GWAS1132602_Hrheumatoid arthritis QTL GWAS1132602 (human)0.000003joint integrity trait (VT:0010548)139229363192293632Human
628726033GWAS2634262_Hglypican-5 measurement QTL GWAS2634262 (human)1e-22glypican-5 measurement139184028591840286Human
597271537GWAS1367611_Hglypican-5 measurement QTL GWAS1367611 (human)2e-12glypican-5 measurement139212684692126847Human
628726032GWAS2634261_Hglypican-5 measurement QTL GWAS2634261 (human)2e-16glypican-5 measurement139165302391653024Human
597271536GWAS1367610_Hglypican-5 measurement QTL GWAS1367610 (human)1e-12glypican-5 measurement139172733191727332Human
597269488GWAS1365562_Htaste liking measurement QTL GWAS1365562 (human)1e-09taste liking measurement139278039392780394Human
626462525GWAS2276458_Hhigh density lipoprotein cholesterol measurement QTL GWAS2276458 (human)3e-12high density lipoprotein cholesterol measurement139175524991755250Human
628726034GWAS2634263_Hglypican-5 measurement QTL GWAS2634263 (human)5e-74glypican-5 measurement139178245191782452Human
407115304GWAS764280_Hself reported educational attainment QTL GWAS764280 (human)4e-09self reported educational attainment139267896992678970Human
407078957GWAS727933_H1,3,7-trimethylurate measurement QTL GWAS727933 (human)0.0000011,3,7-trimethylurate measurement139154564091545641Human
407241768GWAS890744_Hlifestyle measurement, maximum cigarettes per day measurement QTL GWAS890744 (human)0.0000001lifestyle measurement, maximum cigarettes per day measurement139265763892657639Human
628726026GWAS2634255_Hglypican-5 measurement QTL GWAS2634255 (human)3e-15glypican-5 measurement139183800391838004Human
597271533GWAS1367607_Hglypican-5 measurement QTL GWAS1367607 (human)1e-25glypican-5 measurement139139865691398657Human
628793614GWAS2701843_HAlzheimer disease, APOE carrier status QTL GWAS2701843 (human)0.000008Alzheimer disease, APOE carrier status139243907392439074Human
597271532GWAS1367606_Hglypican-5 measurement QTL GWAS1367606 (human)4e-28glypican-5 measurement139200524392005244Human
628726028GWAS2634257_Hglypican-5 measurement QTL GWAS2634257 (human)2e-23glypican-5 measurement139239237292392373Human
628726031GWAS2634260_Hglypican-5 measurement QTL GWAS2634260 (human)4e-292glypican-5 measurement139141774491417745Human
597271535GWAS1367609_Hglypican-5 measurement QTL GWAS1367609 (human)1e-14glypican-5 measurement139181893791818938Human
628650254GWAS2558483_Hfms-related tyrosine kinase 3 ligand measurement QTL GWAS2558483 (human)0.000008fms-related tyrosine kinase 3 ligand measurement139263298392632984Human
597271534GWAS1367608_Hglypican-5 measurement QTL GWAS1367608 (human)3e-15glypican-5 measurement139178393491783935Human
628726017GWAS2634246_Hglypican-5 measurement QTL GWAS2634246 (human)2e-18glypican-5 measurement139156397891563979Human
628724481GWAS2632710_Hglypican-5 measurement QTL GWAS2632710 (human)8e-25glypican-5 measurement139168867591688676Human
628726016GWAS2634245_Hglypican-5 measurement QTL GWAS2634245 (human)4e-66glypican-5 measurement139197475591974756Human
628726019GWAS2634248_Hglypican-5 measurement QTL GWAS2634248 (human)6e-24glypican-5 measurement139183649691836497Human
628724483GWAS2632712_Hglypican-5 measurement QTL GWAS2632712 (human)8e-206glypican-5 measurement139186930691869307Human
628876545GWAS2784774_Hsex interaction measurement, longitudinal BMI measurement QTL GWAS2784774 (human)0.000001body mass (VT:0001259)body mass index (BMI) (CMO:0000105)139215225392152254Human
628724482GWAS2632711_Hglypican-5 measurement QTL GWAS2632711 (human)1e-13glypican-5 measurement139182232291822323Human
597036525GWAS1132599_Hrheumatoid arthritis QTL GWAS1132599 (human)3e-09joint integrity trait (VT:0010548)139229363192293632Human
407129663GWAS778639_Hlipid measurement QTL GWAS778639 (human)0.0000001lipid amount (VT:0001547)blood lipid measurement (CMO:0000050)139267089392670894Human
406997561GWAS646537_Hbiological sex QTL GWAS646537 (human)2e-08biological sex139280846992808470Human
628724484GWAS2632713_Hglypican-5 measurement QTL GWAS2632713 (human)3e-12glypican-5 measurement139220981092209811Human
597083412GWAS1179486_Hprotein measurement QTL GWAS1179486 (human)2e-17protein amount (VT:0010120)139176480491764805Human
628823545GWAS2731774_Hglypican-5 measurement QTL GWAS2731774 (human)1e-83glypican-5 measurement139176480491764805Human
628823544GWAS2731773_Hglypican-5 measurement QTL GWAS2731773 (human)2e-13glypican-5 measurement139140663491406635Human
628763134GWAS2671363_Hbreast density QTL GWAS2671363 (human)0.000006breast density139148122791481228Human
628438512GWAS2346741_Hendometriosis QTL GWAS2346741 (human)0.000007uterus integrity trait (VT:0010575)139198533191985332Human
406889158GWAS538134_Hbreast carcinoma QTL GWAS538134 (human)0.000004breast carcinoma139190303191903032Human
628823543GWAS2731772_Hglypican-5 measurement QTL GWAS2731772 (human)3e-15glypican-5 measurement139194030191940302Human
406939340GWAS588316_Hglypican-5 measurement QTL GWAS588316 (human)2e-10glypican-5 measurement139169302191693022Human
406939346GWAS588322_Hglypican-5 measurement QTL GWAS588322 (human)5e-35glypican-5 measurement139142626891426269Human
628879855GWAS2788084_Hbody height QTL GWAS2788084 (human)1e-09body height139146004191460042Human
597302542GWAS1398616_Hglypican-5 measurement QTL GWAS1398616 (human)2e-22glypican-5 measurement139176480491764805Human
628771812GWAS2680041_Hanxiety measurement, non-high density lipoprotein cholesterol measurement QTL GWAS2680041 (human)8e-118blood non-HDL cholesterol amount (VT:0010474)blood non-high density lipoprotein cholesterol level (CMO:0003967)139247897792478978Human
617290324GWAS2227100_HCleft palate, cleft lip QTL GWAS2227100 (human)0.0000003Cleft palate, cleft lip139196446491964465Human
407014109GWAS663085_Hchronotype measurement QTL GWAS663085 (human)3e-09chronotype measurement139286436792864368Human
628877275GWAS2785504_Hinsomnia QTL GWAS2785504 (human)4e-08sleep behavior trait (VT:0001501)139224525592245256Human
628898270GWAS2806499_Heducational attainment QTL GWAS2806499 (human)1e-10educational attainment139225326892253269Human
628898271GWAS2806500_Heducational attainment QTL GWAS2806500 (human)0.0000001educational attainment139253965292539653Human
597198141GWAS1294215_Hglypican-5 measurement QTL GWAS1294215 (human)2e-45glypican-5 measurement139145296391452964Human
407048422GWAS697398_HHIV-1 infection QTL GWAS697398 (human)0.000005response to viral infection trait (VT:0010439)139256122392561224Human
597198142GWAS1294216_Hglypican-5 measurement QTL GWAS1294216 (human)7e-332glypican-5 measurement139176246191762462Human
407166701GWAS815677_Halpha-tocopherol measurement QTL GWAS815677 (human)0.000002alpha-tocopherol measurement139241317492413175Human
628726227GWAS2634456_Hglypican-5 measurement QTL GWAS2634456 (human)3e-18glypican-5 measurement139248480492484805Human
628726226GWAS2634455_Hglypican-5 measurement QTL GWAS2634455 (human)3e-13glypican-5 measurement139197412891974129Human
628726229GWAS2634458_Hglypican-5 measurement QTL GWAS2634458 (human)6e-208glypican-5 measurement139182712491827125Human
628726228GWAS2634457_Hglypican-5 measurement QTL GWAS2634457 (human)2e-15glypican-5 measurement139208231792082318Human
628726230GWAS2634459_Hglypican-5 measurement QTL GWAS2634459 (human)2e-23glypican-5 measurement139248427492484275Human
628726217GWAS2634446_Hglypican-5 measurement QTL GWAS2634446 (human)8e-27glypican-5 measurement139164447691644477Human
597280041GWAS1376115_Hinsomnia QTL GWAS1376115 (human)4e-08insomnia139224525592245256Human
628726218GWAS2634447_Hglypican-5 measurement QTL GWAS2634447 (human)1e-11glypican-5 measurement139140910591409106Human
628928975GWAS2837204_Hnon-small cell lung carcinoma QTL GWAS2837204 (human)0.000009lung integrity trait (VT:0010906)139167394191673942Human
628726221GWAS2634450_Hglypican-5 measurement QTL GWAS2634450 (human)9e-53glypican-5 measurement139179786791797868Human
597050147GWAS1146221_Hendometriosis QTL GWAS1146221 (human)0.000007endometriosis139198533191985332Human
628897225GWAS2805454_Hinsomnia QTL GWAS2805454 (human)4e-15sleep behavior trait (VT:0001501)139224525592245256Human
628726223GWAS2634452_Hglypican-5 measurement QTL GWAS2634452 (human)7e-13glypican-5 measurement139220437692204377Human
628897226GWAS2805455_Hinsomnia QTL GWAS2805455 (human)4e-11sleep behavior trait (VT:0001501)139225663792256638Human
407205106GWAS854082_Hblood protein measurement QTL GWAS854082 (human)2e-56blood protein measurement139143138191431382Human
628726222GWAS2634451_Hglypican-5 measurement QTL GWAS2634451 (human)2e-23glypican-5 measurement139232047992320480Human
407028469GWAS677445_Hresponse to antineoplastic agent, response to antimicrotubule agent QTL GWAS677445 (human)0.000001response to antineoplastic agent, response to antimicrotubule agent139243639892436399Human
628503489GWAS2411718_Hbiological sex QTL GWAS2411718 (human)2e-08biological sex139280846992808470Human
628724673GWAS2632902_Hglypican-5 measurement QTL GWAS2632902 (human)4e-123glypican-5 measurement139157201991572020Human
628840386GWAS2748615_Hglypican-5 measurement QTL GWAS2748615 (human)6e-130glypican-5 measurement139176480491764805Human
628724672GWAS2632901_Hglypican-5 measurement QTL GWAS2632901 (human)5e-27glypican-5 measurement139212192692121927Human
628861377GWAS2769606_Hsmoking initiation QTL GWAS2769606 (human)2e-09behavior trait (VT:0010442)139239347092393471Human
628724674GWAS2632903_Hglypican-5 measurement QTL GWAS2632903 (human)1e-211glypican-5 measurement139184394391843944Human
406982393GWAS631369_Hblood protein measurement QTL GWAS631369 (human)1e-10blood protein measurement139202820592028206Human
628404687GWAS2312916_Hblood protein amount QTL GWAS2312916 (human)0.000002blood protein amount139242573092425731Human
628770756GWAS2678985_Hcleft lip QTL GWAS2678985 (human)0.000008cleft lip139269155592691556Human
628872635GWAS2780864_Hglypican-5 measurement QTL GWAS2780864 (human)1e-781glypican-5 measurement139176480491764805Human
628724665GWAS2632894_Hglypican-5 measurement QTL GWAS2632894 (human)8e-22glypican-5 measurement139206609892066099Human
616958470GWAS1975969_Hgrowth-regulated alpha protein measurement QTL GWAS1975969 (human)0.000006growth-regulated alpha protein measurement139249010992490110Human
628724664GWAS2632893_Hglypican-5 measurement QTL GWAS2632893 (human)4e-113glypican-5 measurement139205173292051733Human
628997052GWAS2905281_Hconnective tissue disease QTL GWAS2905281 (human)2e-11connective tissue disease139279849192798492Human
616479356GWAS1875939_Hblood protein amount QTL GWAS1875939 (human)0.000002blood protein amount139242573092425731Human
628724667GWAS2632896_Hglypican-5 measurement QTL GWAS2632896 (human)7e-16glypican-5 measurement139243966992439670Human
628724666GWAS2632895_Hglypican-5 measurement QTL GWAS2632895 (human)6e-14glypican-5 measurement139153122491531225Human
628724669GWAS2632898_Hglypican-5 measurement QTL GWAS2632898 (human)3e-74glypican-5 measurement139186758291867583Human
628724668GWAS2632897_Hglypican-5 measurement QTL GWAS2632897 (human)1e-52glypican-5 measurement139192765191927652Human
628872636GWAS2780865_Hglypican-5 measurement QTL GWAS2780865 (human)2e-10glypican-5 measurement139169302191693022Human
628724670GWAS2632899_Hglypican-5 measurement QTL GWAS2632899 (human)4e-22glypican-5 measurement139217103392171034Human
597327191GWAS1423265_Hcolor vision disorder QTL GWAS1423265 (human)0.000009color vision disorder139160933491609335Human
628724663GWAS2632892_Hglypican-5 measurement QTL GWAS2632892 (human)5e-181glypican-5 measurement139175413291754133Human
628724662GWAS2632891_Hglypican-5 measurement QTL GWAS2632891 (human)6e-15glypican-5 measurement139223054692230547Human
406939281GWAS588257_Hglypican-5 measurement QTL GWAS588257 (human)1e-781glypican-5 measurement139176480491764805Human
406983314GWAS632290_Hendometriosis QTL GWAS632290 (human)0.000007endometriosis139198533191985332Human
616541806GWAS1938389_Hglypican-5 measurement QTL GWAS1938389 (human)5e-181glypican-5 measurement139175413291754133Human
616541805GWAS1938388_Hglypican-5 measurement QTL GWAS1938388 (human)6e-15glypican-5 measurement139223054692230547Human
616541801GWAS1938384_Hglypican-5 measurement QTL GWAS1938384 (human)3e-12glypican-5 measurement139220981092209811Human
617186847GWAS2167287_Hanxiety measurement, non-high density lipoprotein cholesterol measurement QTL GWAS2167287 (human)1e-113anxiety measurement, non-high density lipoprotein cholesterol measurement139247897792478978Human
616541800GWAS1938383_Hglypican-5 measurement QTL GWAS1938383 (human)8e-206glypican-5 measurement139186930691869307Human
616496745GWAS1893328_Hcystine measurement QTL GWAS1893328 (human)0.000007cystine measurement139221299692212997Human
616541799GWAS1938382_Hglypican-5 measurement QTL GWAS1938382 (human)1e-13glypican-5 measurement139182232291822323Human
616541798GWAS1938381_Hglypican-5 measurement QTL GWAS1938381 (human)8e-25glypican-5 measurement139168867591688676Human
628627362GWAS2535591_HFEV/FVC ratio QTL GWAS2535591 (human)5e-10lung capacity (VT:0001942)forced expiratory volume to forced vital capacity ratio (CMO:0000241)139178462291784623Human
616541796GWAS1938379_Hglypican-5 measurement QTL GWAS1938379 (human)3e-15glypican-5 measurement139183800391838004Human
628872615GWAS2780844_Hglypican-5 measurement QTL GWAS2780844 (human)5e-35glypican-5 measurement139142626891426269Human
628838309GWAS2746538_Halpha-tocopherol measurement QTL GWAS2746538 (human)0.000002blood vitamin amount (VT:0010626)139241317492413175Human
628565929GWAS2474158_Htaste liking measurement QTL GWAS2474158 (human)1e-09gustatory system physiology trait (VT:0001985)139278039392780394Human
597122935GWAS1219009_Hblood protein measurement QTL GWAS1219009 (human)2e-56blood protein measurement139143138191431382Human
407185057GWAS834033_Hglypican-5 measurement QTL GWAS834033 (human)2e-22glypican-5 measurement139176480491764805Human
616358490GWAS1843205_Hgut microbiome measurement, allergen exposure measurement QTL GWAS1843205 (human)2e-09gut microbiome measurement, allergen exposure measurement139267651092676511Human
597178736GWAS1274810_Hglypican-5 measurement QTL GWAS1274810 (human)5e-35glypican-5 measurement139142626891426269Human
597112189GWAS1208263_Hblood protein measurement QTL GWAS1208263 (human)1e-36blood protein measurement139179962991799630Human
407129768GWAS778744_Hmultiple sclerosis QTL GWAS778744 (human)0.000001multiple sclerosis139267963392679634Human
598067531GWAS1786830_Hbody height QTL GWAS1786830 (human)3e-10body height139213559192135592Human
407227562GWAS876538_Hbone density QTL GWAS876538 (human)1e-10bone density139163794991637950Human
407274167GWAS923143_Hbody height QTL GWAS923143 (human)3e-10body height139213559192135592Human
616539722GWAS1936305_Hglypican-5 measurement QTL GWAS1936305 (human)1e-211glypican-5 measurement139184394391843944Human
616539721GWAS1936304_Hglypican-5 measurement QTL GWAS1936304 (human)4e-123glypican-5 measurement139157201991572020Human
616539720GWAS1936303_Hglypican-5 measurement QTL GWAS1936303 (human)5e-27glypican-5 measurement139212192692121927Human
598146908GWAS1833636_Hurate measurement, bone tissue density QTL GWAS1833636 (human)3e-13urate measurement, bone tissue density139194444891944449Human
597824862GWAS1692253_Hurate measurement QTL GWAS1692253 (human)3e-13urate measurement139194444891944449Human
407028927GWAS677903_Hphysical activity QTL GWAS677903 (human)0.0000004physical activity139184941091849411Human
407169210GWAS818186_Hcervical cancer QTL GWAS818186 (human)0.000003cervical cancer139161842391618424Human
628666246GWAS2574475_Hbone tissue density QTL GWAS2574475 (human)1e-10bone tissue density139163794991637950Human
598141272GWAS1828000_Hpancreatic intraductal papillary-mucinous neoplasm QTL GWAS1828000 (human)2e-08pancreatic intraductal papillary-mucinous neoplasm139216806292168063Human
628418443GWAS2326672_HAstigmatism QTL GWAS2326672 (human)0.000008Astigmatism139250020592500206Human
597178520GWAS1274594_Hglypican-5 measurement QTL GWAS1274594 (human)1e-781glypican-5 measurement139176480491764805Human
597178521GWAS1274595_Hglypican-5 measurement QTL GWAS1274595 (human)2e-10glypican-5 measurement139169302191693022Human
406998339GWAS647315_Hforced expiratory volume QTL GWAS647315 (human)4e-12forced expiratory volume139178356491783565Human
616358847GWAS1843562_Hgut microbiome measurement, allergen exposure measurement QTL GWAS1843562 (human)4e-08gut microbiome measurement, allergen exposure measurement139285598392855984Human
616541115GWAS1937698_Hglypican-5 measurement QTL GWAS1937698 (human)9e-53glypican-5 measurement139179786791797868Human
406982470GWAS631446_Hblood protein measurement QTL GWAS631446 (human)1e-36blood protein measurement139179962991799630Human
597173404GWAS1269478_Heducational attainment QTL GWAS1269478 (human)1e-10educational attainment139225326892253269Human
616986563GWAS2004062_HAstigmatism QTL GWAS2004062 (human)0.000008Astigmatism139250020592500206Human
597173405GWAS1269479_Heducational attainment QTL GWAS1269479 (human)0.0000001educational attainment139253965292539653Human
616541112GWAS1937695_Hglypican-5 measurement QTL GWAS1937695 (human)4e-292glypican-5 measurement139141774491417745Human
597274782GWAS1370856_Hglypican-5 measurement QTL GWAS1370856 (human)6e-130glypican-5 measurement139176480491764805Human
617143232GWAS2160731_Hglypican-5 measurement QTL GWAS2160731 (human)2e-31glypican-5 measurement139178989191789892Human
616483766GWAS1880349_Hblood protein amount QTL GWAS1880349 (human)1e-36blood protein amount139179962991799630Human
616483767GWAS1880350_Hblood protein amount QTL GWAS1880350 (human)1e-10blood protein amount139202820592028206Human
597429910GWAS1525984_Hprotein measurement QTL GWAS1525984 (human)1e-23protein measurement139178517691785177Human
616541109GWAS1937692_Hglypican-5 measurement QTL GWAS1937692 (human)2e-23glypican-5 measurement139239237292392373Human
616541108GWAS1937691_Hglypican-5 measurement QTL GWAS1937691 (human)1e-11glypican-5 measurement139140910591409106Human
616541107GWAS1937690_Hglypican-5 measurement QTL GWAS1937690 (human)8e-27glypican-5 measurement139164447691644477Human
616541106GWAS1937689_Hglypican-5 measurement QTL GWAS1937689 (human)5e-74glypican-5 measurement139178245191782452Human
625818691GWAS2239613_Hhealth trait QTL GWAS2239613 (human)2e-08health trait139144181691441817Human
616541105GWAS1937688_Hglypican-5 measurement QTL GWAS1937688 (human)1e-22glypican-5 measurement139184028591840286Human
616541104GWAS1937687_Hglypican-5 measurement QTL GWAS1937687 (human)2e-16glypican-5 measurement139165302391653024Human
597277834GWAS1373908_Hdiet measurement QTL GWAS1373908 (human)5e-08diet measurement139269291792692918Human
616481706GWAS1878289_Hblood protein amount QTL GWAS1878289 (human)2e-56blood protein amount139143138191431382Human
597108867GWAS1204941_Hmathematical ability QTL GWAS1204941 (human)2e-08mathematical ability139271392492713925Human
407155027GWAS804003_HAlzheimer disease, APOE carrier status QTL GWAS804003 (human)0.000008Alzheimer disease, APOE carrier status139243907392439074Human
628584044GWAS2492273_Hglypican-5 measurement QTL GWAS2492273 (human)5e-233glypican-5 measurement139177069291770693Human
597148300GWAS1244374_Hsmoking initiation QTL GWAS1244374 (human)2e-09smoking initiation139239302992393030Human
597252743GWAS1348817_Hurate measurement, bone density QTL GWAS1348817 (human)3e-13urate measurement, bone density139194444891944449Human
407045468GWAS694444_Hphysical activity QTL GWAS694444 (human)0.000005physical activity139184941091849411Human
407256935GWAS905911_Hglypican-5 measurement QTL GWAS905911 (human)6e-130glypican-5 measurement139176480491764805Human
598146176GWAS1832904_Hbone tissue density QTL GWAS1832904 (human)1e-10bone tissue density139163794991637950Human
407347552GWAS996528_Hunipolar depression, memory performance, cognitive function measurement QTL GWAS996528 (human)0.0000003unipolar depression, memory performance, cognitive function measurement139226401592264016Human
628725841GWAS2634070_Hglypican-5 measurement QTL GWAS2634070 (human)4e-190glypican-5 measurement139214869292148693Human
628725843GWAS2634072_Hglypican-5 measurement QTL GWAS2634072 (human)1e-16glypican-5 measurement139179456891794569Human
406958957GWAS607933_Hbreast density QTL GWAS607933 (human)0.000006breast density139148122791481228Human
628725844GWAS2634073_Hglypican-5 measurement QTL GWAS2634073 (human)1e-110glypican-5 measurement139188541691885417Human
407021420GWAS670396_Hresponse to radiation, edema QTL GWAS670396 (human)1e-09response to radiation, edema139228598392285984Human
597336244GWAS1432318_Hsevere acute respiratory syndrome, COVID-19 QTL GWAS1432318 (human)2e-15severe acute respiratory syndrome, COVID-19139262951592629516Human
2289426BW213_HBody weight QTL 213 (human)2.780.0002Body weightBMI1384267977110267977Human
628884548GWAS2792777_Hdiet measurement QTL GWAS2792777 (human)5e-08eating behavior trait (VT:0001431)food intake measurement (CMO:0000772)139269291792692918Human
2289433BW340_HBody weight QTL 340 (human)3.11Body morphometrywaist circumference1384267977110267977Human
407256838GWAS905814_Hglypican-5 measurement QTL GWAS905814 (human)3e-15glypican-5 measurement139178393491783935Human
407256839GWAS905815_Hglypican-5 measurement QTL GWAS905815 (human)1e-14glypican-5 measurement139181893791818938Human
407256836GWAS905812_Hglypican-5 measurement QTL GWAS905812 (human)4e-28glypican-5 measurement139200524392005244Human
407256837GWAS905813_Hglypican-5 measurement QTL GWAS905813 (human)1e-25glypican-5 measurement139139865691398657Human
597319897GWAS1415971_Hsmoking initiation QTL GWAS1415971 (human)2e-09smoking initiation139239347092393471Human
407244544GWAS893520_Hforced expiratory volume QTL GWAS893520 (human)2e-08forced expiratory volume139179252491792525Human
597118170GWAS1214244_Hforced expiratory volume QTL GWAS1214244 (human)2e-08forced expiratory volume139179252491792525Human
407256840GWAS905816_Hglypican-5 measurement QTL GWAS905816 (human)1e-12glypican-5 measurement139172733191727332Human
407256841GWAS905817_Hglypican-5 measurement QTL GWAS905817 (human)2e-12glypican-5 measurement139212684692126847Human
628452410GWAS2360639_Hself reported educational attainment QTL GWAS2360639 (human)4e-09self reported educational attainment139267896992678970Human
628699176GWAS2607405_Hbrain attribute QTL GWAS2607405 (human)2e-08brain attribute139219971592199716Human
598063863GWAS1783162_Hbrain attribute QTL GWAS1783162 (human)2e-08brain attribute139219971592199716Human
406940434GWAS589410_Hprotein measurement QTL GWAS589410 (human)2e-17protein measurement139176480491764805Human
616378345GWAS1858587_Hobsolete_blood protein measurement QTL GWAS1858587 (human)2e-218obsolete_blood protein measurement139177069291770693Human
406963991GWAS612967_Hsevere acute respiratory syndrome, COVID-19 QTL GWAS612967 (human)2e-15severe acute respiratory syndrome, COVID-19139262951592629516Human
628857379GWAS2765608_HCOVID-19 QTL GWAS2765608 (human)0.0000007COVID-19139144034491440345Human
597104334GWAS1200408_Hreading and spelling ability QTL GWAS1200408 (human)0.000008cognitive behavior trait (VT:0010450)139141682091416821Human
407022363GWAS671339_Hsex interaction measurement, longitudinal BMI measurement QTL GWAS671339 (human)0.000001sex interaction measurement, longitudinal BMI measurement139215225392152254Human
628460586GWAS2368815_Hmathematical ability QTL GWAS2368815 (human)2e-08cognitive behavior trait (VT:0010450)139271392492713925Human
628984860GWAS2893089_HArthropathy QTL GWAS2893089 (human)1e-11Arthropathy139167167591671676Human
406977315GWAS626291_Hblood protein measurement QTL GWAS626291 (human)0.000002blood protein measurement139242573092425731Human
628753944GWAS2662173_Holigodendroglioma QTL GWAS2662173 (human)0.000005oligodendroglioma139258335592583356Human
597226235GWAS1322309_Hchronotype measurement QTL GWAS1322309 (human)3e-09chronotype measurement139286436792864368Human
407058724GWAS707700_HTetralogy of Fallot QTL GWAS707700 (human)3e-09Tetralogy of Fallot139233607092336071Human
407044392GWAS693368_HTinnitus QTL GWAS693368 (human)0.000001Tinnitus139238861392388614Human
628367364GWAS2288208_Hlung carcinoma QTL GWAS2288208 (human)0.0000002lung carcinoma139167394191673942Human
617143225GWAS2160724_Hglypican-5 measurement QTL GWAS2160724 (human)3e-13glypican-5 measurement139197412891974129Human
617143226GWAS2160725_Hglypican-5 measurement QTL GWAS2160725 (human)2e-15glypican-5 measurement139208231792082318Human
617143227GWAS2160726_Hglypican-5 measurement QTL GWAS2160726 (human)2e-23glypican-5 measurement139248427492484275Human
597144290GWAS1240364_HCOVID-19 QTL GWAS1240364 (human)0.0000007COVID-19139144034491440345Human
617143229GWAS2160728_Hglypican-5 measurement QTL GWAS2160728 (human)1e-16glypican-5 measurement139179456891794569Human
617143230GWAS2160729_Hglypican-5 measurement QTL GWAS2160729 (human)1e-110glypican-5 measurement139188541691885417Human
617143231GWAS2160730_Hglypican-5 measurement QTL GWAS2160730 (human)9e-24glypican-5 measurement139194339091943391Human
597112544GWAS1208618_Hblood protein measurement QTL GWAS1208618 (human)1e-10blood protein measurement139202820592028206Human
617186224GWAS2166664_Hanxiety measurement, non-high density lipoprotein cholesterol measurement QTL GWAS2166664 (human)8e-118anxiety measurement, non-high density lipoprotein cholesterol measurement139247897792478978Human
597615844GWAS1672704_HArthropathy QTL GWAS1672704 (human)1e-11Arthropathy139167167591671676Human
597829342GWAS1696733_Hfms-related tyrosine kinase 3 ligand measurement QTL GWAS1696733 (human)0.000008fms-related tyrosine kinase 3 ligand measurement139263298392632984Human
407374645GWAS1023621_HAstigmatism QTL GWAS1023621 (human)0.000008Astigmatism139250020592500206Human
598077476GWAS1796775_Hbone density QTL GWAS1796775 (human)1e-10bone density139163794991637950Human
617139530GWAS2157029_Hglypican-5 measurement QTL GWAS2157029 (human)1e-211glypican-5 measurement139184394391843944Human
628726011GWAS2634240_Hglypican-5 measurement QTL GWAS2634240 (human)9e-24glypican-5 measurement139194339091943391Human
628726013GWAS2634242_Hglypican-5 measurement QTL GWAS2634242 (human)9e-12glypican-5 measurement139214680092146801Human
628726012GWAS2634241_Hglypican-5 measurement QTL GWAS2634241 (human)2e-31glypican-5 measurement139178989191789892Human
628726014GWAS2634243_Hglypican-5 measurement QTL GWAS2634243 (human)2e-22glypican-5 measurement139163202491632025Human
597327890GWAS1423964_Hbreast density QTL GWAS1423964 (human)0.000006breast density139148122791481228Human
406905288GWAS554264_HBMI-adjusted waist circumference QTL GWAS554264 (human)0.000003BMI-adjusted waist circumference139190589091905891Human
406934473GWAS583449_Hsmoking initiation QTL GWAS583449 (human)2e-09smoking initiation139239302992393030Human
407112654GWAS761630_Hmathematical ability QTL GWAS761630 (human)2e-08mathematical ability139271392492713925Human
597315606GWAS1411680_H1,3,7-trimethylurate measurement QTL GWAS1411680 (human)0.0000011,3,7-trimethylurate measurement139154564091545641Human
628656375GWAS2564604_Hcolor vision disorder QTL GWAS2564604 (human)0.000009color vision disorder139160933491609335Human
628485882GWAS2394111_Hblood protein amount QTL GWAS2394111 (human)2e-218blood protein amount139177069291770693Human
628453626GWAS2361855_Hchronotype measurement QTL GWAS2361855 (human)3e-09sleep behavior trait (VT:0001501)139286436792864368Human
597173769GWAS1269843_HTinnitus QTL GWAS1269843 (human)0.000001Tinnitus139238861392388614Human
597617167GWAS1674027_Hconnective tissue disease QTL GWAS1674027 (human)2e-11connective tissue disease139279849192798492Human
628690158GWAS2598387_Hglypican-5 measurement QTL GWAS2598387 (human)2e-22glypican-5 measurement139176480491764805Human
617186142GWAS2166582_Hanxiety measurement, triglyceride measurement QTL GWAS2166582 (human)3e-10anxiety measurement, triglyceride measurement139247897792478978Human
628841187GWAS2749416_Hglypican-5 measurement QTL GWAS2749416 (human)1e-25glypican-5 measurement139139865691398657Human
597327362GWAS1423436_Hforced expiratory volume QTL GWAS1423436 (human)4e-12forced expiratory volume139178356491783565Human
628522223GWAS2430452_Hhealth trait QTL GWAS2430452 (human)2e-08health trait139144181691441817Human
628841186GWAS2749415_Hglypican-5 measurement QTL GWAS2749415 (human)4e-28glypican-5 measurement139200524392005244Human
597121549GWAS1217623_Hcleft lip QTL GWAS1217623 (human)0.000008cleft lip139269155592691556Human
597060618GWAS1156692_HFEV/FVC ratio QTL GWAS1156692 (human)5e-10FEV/FVC ratio139178462291784623Human
628841191GWAS2749420_Hglypican-5 measurement QTL GWAS2749420 (human)2e-12glypican-5 measurement139212684692126847Human
616375584GWAS1855826_Hobsolete_blood protein measurement QTL GWAS1855826 (human)2e-56obsolete_blood protein measurement139143138191431382Human
628841190GWAS2749419_Hglypican-5 measurement QTL GWAS2749419 (human)1e-12glypican-5 measurement139172733191727332Human
628924129GWAS2832358_Hcathepsin D measurement QTL GWAS2832358 (human)2e-14cathepsin D measurement139176480491764805Human
597022728GWAS1118802_Hbreast carcinoma QTL GWAS1118802 (human)0.000004mammary gland integrity trait (VT:0010552)139190303191903032Human
407393237GWAS1042213_Hurate measurement, bone density QTL GWAS1042213 (human)3e-13urate measurement, bone density139194444891944449Human
628841189GWAS2749418_Hglypican-5 measurement QTL GWAS2749418 (human)1e-14glypican-5 measurement139181893791818938Human
628841188GWAS2749417_Hglypican-5 measurement QTL GWAS2749417 (human)3e-15glypican-5 measurement139178393491783935Human
628920540GWAS2828769_Hhigh density lipoprotein cholesterol measurement QTL GWAS2828769 (human)3e-12blood HDL cholesterol amount (VT:0000184)blood high density lipoprotein cholesterol level (CMO:0000052)139175524991755250Human
616541463GWAS1938046_Hglypican-5 measurement QTL GWAS1938046 (human)6e-24glypican-5 measurement139183649691836497Human
616541461GWAS1938044_Hglypican-5 measurement QTL GWAS1938044 (human)2e-18glypican-5 measurement139156397891563979Human
616541460GWAS1938043_Hglypican-5 measurement QTL GWAS1938043 (human)4e-66glypican-5 measurement139197475591974756Human
628889815GWAS2798044_Hmemory performance, cognitive function measurement, major depressive disorder QTL GWAS2798044 (human)0.0000003cognitive behavior trait (VT:0010450)139226401592264016Human
616541458GWAS1938041_Hglypican-5 measurement QTL GWAS1938041 (human)2e-22glypican-5 measurement139163202491632025Human
616369424GWAS1849666_Hobsolete_blood protein measurement QTL GWAS1849666 (human)0.000002obsolete_blood protein measurement139242573092425731Human
616541457GWAS1938040_Hglypican-5 measurement QTL GWAS1938040 (human)9e-12glypican-5 measurement139214680092146801Human
616541456GWAS1938039_Hglypican-5 measurement QTL GWAS1938039 (human)2e-31glypican-5 measurement139178989191789892Human
616541455GWAS1938038_Hglypican-5 measurement QTL GWAS1938038 (human)9e-24glypican-5 measurement139194339091943391Human
628643016GWAS2551245_Hgut microbiome measurement, allergen exposure measurement QTL GWAS2551245 (human)2e-09gut microbiome measurement, allergen exposure measurement139267651092676511Human
616541454GWAS1938037_Hglypican-5 measurement QTL GWAS1938037 (human)1e-110glypican-5 measurement139188541691885417Human
616541453GWAS1938036_Hglypican-5 measurement QTL GWAS1938036 (human)1e-16glypican-5 measurement139179456891794569Human
407020529GWAS669505_Hnephrotic syndrome QTL GWAS669505 (human)0.0000003kidney integrity trait (VT:0010580)139155155991551560Human
628368583GWAS2289427_Hcathepsin D measurement QTL GWAS2289427 (human)2e-14cathepsin D measurement139176480491764805Human
616541451GWAS1938034_Hglypican-5 measurement QTL GWAS1938034 (human)4e-190glypican-5 measurement139214869292148693Human
616541448GWAS1938031_Hglypican-5 measurement QTL GWAS1938031 (human)2e-23glypican-5 measurement139248427492484275Human
616541447GWAS1938030_Hglypican-5 measurement QTL GWAS1938030 (human)6e-208glypican-5 measurement139182712491827125Human
616541446GWAS1938029_Hglypican-5 measurement QTL GWAS1938029 (human)2e-15glypican-5 measurement139208231792082318Human
628574925GWAS2483154_Hforced expiratory volume QTL GWAS2483154 (human)2e-08lung capacity (VT:0001942)forced expiratory volume (CMO:0000254)139179252491792525Human
616541445GWAS1938028_Hglypican-5 measurement QTL GWAS1938028 (human)3e-18glypican-5 measurement139248480492484805Human
616541444GWAS1938027_Hglypican-5 measurement QTL GWAS1938027 (human)3e-13glypican-5 measurement139197412891974129Human
616475906GWAS1872489_Hblood protein amount QTL GWAS1872489 (human)2e-218blood protein amount139177069291770693Human
616541441GWAS1938024_Hglypican-5 measurement QTL GWAS1938024 (human)7e-13glypican-5 measurement139220437692204377Human
616539392GWAS1935975_Hglypican-5 measurement QTL GWAS1935975 (human)4e-22glypican-5 measurement139217103392171034Human
616541440GWAS1938023_Hglypican-5 measurement QTL GWAS1938023 (human)2e-23glypican-5 measurement139232047992320480Human
628908732GWAS2816961_HCleft palate, cleft lip QTL GWAS2816961 (human)0.0000003Cleft palate, cleft lip139196446491964465Human
628646073GWAS2554302_Hgut microbiome measurement, allergen exposure measurement QTL GWAS2554302 (human)4e-08gut microbiome measurement, allergen exposure measurement139285598392855984Human
407324035GWAS973011_Hinsomnia QTL GWAS973011 (human)4e-11insomnia139225663792256638Human
628859583GWAS2767812_Hsmoking initiation QTL GWAS2767812 (human)2e-09behavior trait (VT:0010442)139239302992393030Human
407324034GWAS973010_Hinsomnia QTL GWAS973010 (human)4e-15insomnia139224525592245256Human
407316352GWAS965328_Hdiet measurement QTL GWAS965328 (human)5e-08diet measurement139269291792692918Human
407071627GWAS720603_Heducational attainment QTL GWAS720603 (human)1e-10educational attainment139225326892253269Human
596974173GWAS1093692_Hmemory performance, cognitive function measurement, major depressive disorder QTL GWAS1093692 (human)0.0000003memory performance, cognitive function measurement, major depressive disorder139226401592264016Human
617137920GWAS2155419_Hglypican-5 measurement QTL GWAS2155419 (human)7e-16glypican-5 measurement139243966992439670Human
617137921GWAS2155420_Hglypican-5 measurement QTL GWAS2155420 (human)4e-22glypican-5 measurement139217103392171034Human
597038685GWAS1134759_Hgut microbiome measurement QTL GWAS1134759 (human)0.000005gut microbiome measurement139190458091904581Human
617137923GWAS2155422_Hglypican-5 measurement QTL GWAS2155422 (human)5e-27glypican-5 measurement139212192692121927Human
625827456GWAS2248378_Hbody height QTL GWAS2248378 (human)1e-09body height139146004191460042Human
407156105GWAS805081_Hgut microbiome measurement QTL GWAS805081 (human)0.000005gut microbiome measurement139190458091904581Human
597249111GWAS1345185_Hcervical cancer QTL GWAS1345185 (human)0.000003cervical cancer139161842391618424Human
597199447GWAS1295521_Hbone density QTL GWAS1295521 (human)1e-10bone density139163794991637950Human
628593336GWAS2501565_Hlifestyle measurement, maximum cigarettes per day measurement QTL GWAS2501565 (human)0.0000001response to nicotine trait (VT:0010721)139265763892657639Human
597297230GWAS1393304_Hglypican-5 measurement QTL GWAS1393304 (human)2e-13glypican-5 measurement139140663491406635Human
628367520GWAS2288364_Hnon-small cell lung carcinoma QTL GWAS2288364 (human)0.000009non-small cell lung carcinoma139167394191673942Human
597297231GWAS1393305_Hglypican-5 measurement QTL GWAS1393305 (human)1e-83glypican-5 measurement139176480491764805Human
597297229GWAS1393303_Hglypican-5 measurement QTL GWAS1393303 (human)3e-15glypican-5 measurement139194030191940302Human
628654240GWAS2562469_Hforced expiratory volume QTL GWAS2562469 (human)4e-12lung capacity (VT:0001942)forced expiratory volume (CMO:0000254)139178356491783565Human
407258535GWAS907511_Hglypican-5 measurement QTL GWAS907511 (human)2e-45glypican-5 measurement139145296391452964Human
407297955GWAS946931_Hglypican-5 measurement QTL GWAS946931 (human)6e-167glypican-5 measurement139176480491764805Human
597296765GWAS1392839_Hglypican-5 measurement QTL GWAS1392839 (human)5e-233glypican-5 measurement139177069291770693Human
407198125GWAS847101_Hglypican-5 measurement QTL GWAS847101 (human)1e-83glypican-5 measurement139176480491764805Human
407198124GWAS847100_Hglypican-5 measurement QTL GWAS847100 (human)2e-13glypican-5 measurement139140663491406635Human
407258541GWAS907517_Hglypican-5 measurement QTL GWAS907517 (human)7e-332glypican-5 measurement139176246191762462Human
597533302GWAS1629376_Hmalignant exocrine pancreas neoplasm QTL GWAS1629376 (human)2e-08malignant exocrine pancreas neoplasm139216806292168063Human
407198123GWAS847099_Hglypican-5 measurement QTL GWAS847099 (human)3e-15glypican-5 measurement139194030191940302Human
597323880GWAS1419954_Hinsomnia QTL GWAS1419954 (human)4e-15insomnia139224525592245256Human
628785288GWAS2693517_Hanxiety measurement, triglyceride measurement QTL GWAS2693517 (human)3e-10triglyceride amount (VT:0000187)blood triglyceride level (CMO:0000118)139247897792478978Human
597533294GWAS1629368_Hmalignant exocrine pancreas neoplasm QTL GWAS1629368 (human)0.000001malignant exocrine pancreas neoplasm139216806292168063Human
597323881GWAS1419955_Hinsomnia QTL GWAS1419955 (human)4e-11insomnia139225663792256638Human
598000728GWAS1720027_Hurate measurement, bone density QTL GWAS1720027 (human)3e-13urate measurement, bone density139194444891944449Human
628785286GWAS2693515_Hanxiety measurement, triglyceride measurement QTL GWAS2693515 (human)2e-258triglyceride amount (VT:0000187)blood triglyceride level (CMO:0000118)139247897792478978Human
628783750GWAS2691979_Hanxiety measurement, non-high density lipoprotein cholesterol measurement QTL GWAS2691979 (human)1e-113blood non-HDL cholesterol amount (VT:0010474)blood non-high density lipoprotein cholesterol level (CMO:0003967)139247897792478978Human
617186101GWAS2166541_Hanxiety measurement, triglyceride measurement QTL GWAS2166541 (human)2e-258anxiety measurement, triglyceride measurement139247897792478978Human

Markers in Region
D13S1300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,611,211 - 92,611,419UniSTSGRCh37
Build 361391,409,212 - 91,409,420RGDNCBI36
Celera1373,458,455 - 73,458,663RGD
Cytogenetic Map13q32UniSTS
HuRef1373,207,778 - 73,207,986UniSTS
Marshfield Genetic Map1371.06RGD
Marshfield Genetic Map1371.06UniSTS
Genethon Genetic Map1373.1UniSTS
deCODE Assembly Map1383.0UniSTS
Whitehead-YAC Contig Map13 UniSTS
D13S795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,690,578 - 92,690,689UniSTSGRCh37
Build 361391,488,579 - 91,488,690RGDNCBI36
Celera1373,537,818 - 73,537,929RGD
Cytogenetic Map13q32UniSTS
HuRef1373,287,155 - 73,287,266UniSTS
Marshfield Genetic Map1371.06UniSTS
Marshfield Genetic Map1371.06RGD
deCODE Assembly Map1383.0UniSTS
SGC34864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,646,858 - 92,646,981UniSTSGRCh37
Build 361391,444,859 - 91,444,982RGDNCBI36
Celera1373,494,101 - 73,494,224RGD
Cytogenetic Map13q32UniSTS
HuRef1373,243,423 - 73,243,546UniSTS
GeneMap99-GB4 RH Map13259.21UniSTS
Whitehead-RH Map13238.1UniSTS
STS-T81306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,128,466 - 92,128,706UniSTSGRCh37
Build 361390,926,467 - 90,926,707RGDNCBI36
Celera1372,975,401 - 72,975,641RGD
Cytogenetic Map13q32UniSTS
GeneMap99-GB4 RH Map13256.16UniSTS
NCBI RH Map13674.9UniSTS
WI-15916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,519,350 - 93,519,474UniSTSGRCh37
Build 361392,317,351 - 92,317,475RGDNCBI36
Celera1374,366,597 - 74,366,721RGD
Cytogenetic Map13q32UniSTS
HuRef1374,115,868 - 74,115,992UniSTS
GeneMap99-GB4 RH Map13265.64UniSTS
Whitehead-RH Map13245.1UniSTS
SHGC-53712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,893,701 - 92,893,882UniSTSGRCh37
Build 361391,691,702 - 91,691,883RGDNCBI36
Celera1373,740,953 - 73,741,134RGD
Cytogenetic Map13q32UniSTS
HuRef1373,490,464 - 73,490,645UniSTS
TNG Radiation Hybrid Map1333035.0UniSTS
D13S1690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,955,529 - 92,955,678UniSTSGRCh37
Build 361391,753,530 - 91,753,679RGDNCBI36
Celera1373,802,776 - 73,802,925RGD
Cytogenetic Map13q32UniSTS
HuRef1373,552,279 - 73,552,428UniSTS
L17986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,084,405 - 92,084,743UniSTSGRCh37
Build 361390,882,406 - 90,882,744RGDNCBI36
Celera1372,931,332 - 72,931,668RGD
Cytogenetic Map13q32UniSTS
HuRef1372,680,255 - 72,680,591UniSTS
G29128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,128,545 - 92,128,679UniSTSGRCh37
Build 361390,926,546 - 90,926,680RGDNCBI36
Celera1372,975,480 - 72,975,614RGD
Cytogenetic Map13q32UniSTS
HuRef1372,724,402 - 72,724,536UniSTS
RH93789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,519,171 - 93,519,307UniSTSGRCh37
Build 361392,317,172 - 92,317,308RGDNCBI36
Celera1374,366,418 - 74,366,554RGD
Cytogenetic Map13q32UniSTS
HuRef1374,115,689 - 74,115,825UniSTS
GeneMap99-GB4 RH Map13264.2UniSTS
RH80577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,252,777 - 93,252,914UniSTSGRCh37
Build 361392,050,778 - 92,050,915RGDNCBI36
Celera1374,100,035 - 74,100,172RGD
RH104318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,172,009 - 92,172,143UniSTSGRCh37
Build 361390,970,010 - 90,970,144RGDNCBI36
Celera1373,018,951 - 73,019,085RGD
Cytogenetic Map13q32UniSTS
HuRef1372,768,199 - 72,768,333UniSTS
GeneMap99-GB4 RH Map13257.57UniSTS
SHGC-80699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,378,184 - 93,378,483UniSTSGRCh37
Build 361392,176,185 - 92,176,484RGDNCBI36
Celera1374,225,423 - 74,225,722RGD
Cytogenetic Map13q32UniSTS
HuRef1373,974,692 - 73,974,991UniSTS
TNG Radiation Hybrid Map1333376.0UniSTS
SHGC-81144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,837,679 - 92,838,025UniSTSGRCh37
Build 361391,635,680 - 91,636,026RGDNCBI36
Celera1373,684,938 - 73,685,284RGD
Cytogenetic Map13q32UniSTS
HuRef1373,434,392 - 73,434,738UniSTS
TNG Radiation Hybrid Map1332999.0UniSTS
SHGC-83508  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,609,072 - 92,609,419UniSTSGRCh37
Build 361391,407,073 - 91,407,420RGDNCBI36
Celera1373,456,316 - 73,456,663RGD
Cytogenetic Map13q32UniSTS
HuRef1373,205,639 - 73,205,986UniSTS
TNG Radiation Hybrid Map1332841.0UniSTS
SHGC-86335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,161,989 - 93,162,323UniSTSGRCh37
Build 361391,959,990 - 91,960,324RGDNCBI36
Celera1374,009,028 - 74,009,362RGD
Cytogenetic Map13q32UniSTS
HuRef1373,758,378 - 73,758,712UniSTS
SHGC-84151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,310,003 - 93,310,328UniSTSGRCh37
Build 361392,108,004 - 92,108,329RGDNCBI36
Celera1374,157,271 - 74,157,596RGD
Cytogenetic Map13q32UniSTS
HuRef1373,906,565 - 73,906,890UniSTS
TNG Radiation Hybrid Map1333349.0UniSTS
SHGC-84210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,831,947 - 92,832,268UniSTSGRCh37
Build 361391,629,948 - 91,630,269RGDNCBI36
Celera1373,679,206 - 73,679,527RGD
Cytogenetic Map13q32UniSTS
HuRef1373,428,660 - 73,428,981UniSTS
TNG Radiation Hybrid Map1333007.0UniSTS
SHGC-86221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,380,387 - 92,380,702UniSTSGRCh37
Build 361391,178,388 - 91,178,703RGDNCBI36
Celera1373,227,577 - 73,227,892RGD
Cytogenetic Map13q32UniSTS
HuRef1372,976,898 - 72,977,213UniSTS
TNG Radiation Hybrid Map1332737.0UniSTS
RH120664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,461,926 - 92,462,235UniSTSGRCh37
Build 361391,259,927 - 91,260,236RGDNCBI36
Celera1373,309,133 - 73,309,442RGD
Cytogenetic Map13q32UniSTS
HuRef1373,058,310 - 73,058,619UniSTS
TNG Radiation Hybrid Map157764.0UniSTS
RH119939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,653,542 - 92,653,832UniSTSGRCh37
Build 361391,451,543 - 91,451,833RGDNCBI36
Celera1373,500,785 - 73,501,075RGD
Cytogenetic Map13q32UniSTS
HuRef1373,250,108 - 73,250,398UniSTS
TNG Radiation Hybrid Map1332877.0UniSTS
RH122663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,859,740 - 92,860,073UniSTSGRCh37
Build 361391,657,741 - 91,658,074RGDNCBI36
Celera1373,706,991 - 73,707,324RGD
Cytogenetic Map13q32UniSTS
HuRef1373,456,442 - 73,456,775UniSTS
RH121340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,992,027 - 92,992,369UniSTSGRCh37
Build 361391,790,028 - 91,790,370RGDNCBI36
Celera1373,839,281 - 73,839,623RGD
Cytogenetic Map13q32UniSTS
HuRef1373,588,782 - 73,589,124UniSTS
GDB:314231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,084,255 - 92,084,545UniSTSGRCh37
Build 361390,882,256 - 90,882,546RGDNCBI36
Celera1372,931,182 - 72,931,470RGD
Cytogenetic Map13q32UniSTS
HuRef1372,680,105 - 72,680,393UniSTS
SHGC-143319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,981,807 - 92,982,091UniSTSGRCh37
Build 361391,779,808 - 91,780,092RGDNCBI36
Celera1373,829,062 - 73,829,346RGD
Cytogenetic Map13q32UniSTS
HuRef1373,578,565 - 73,578,849UniSTS
TNG Radiation Hybrid Map1333106.0UniSTS
SHGC-151150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,611,148 - 92,611,270UniSTSGRCh37
Build 361391,409,149 - 91,409,271RGDNCBI36
Celera1373,458,392 - 73,458,514RGD
Cytogenetic Map13q32UniSTS
HuRef1373,207,715 - 73,207,837UniSTS
TNG Radiation Hybrid Map437796.0UniSTS
TNG Radiation Hybrid Map1332832.0UniSTS
SHGC-145290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,304,815 - 92,305,147UniSTSGRCh37
Build 361391,102,816 - 91,103,148RGDNCBI36
Celera1373,152,029 - 73,152,361RGD
Cytogenetic Map13q32UniSTS
HuRef1372,901,347 - 72,901,679UniSTS
TNG Radiation Hybrid Map1332715.0UniSTS
SHGC-51851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,496,178 - 92,496,370UniSTSGRCh37
Build 361391,294,179 - 91,294,371RGDNCBI36
Celera1373,343,373 - 73,343,565RGD
Cytogenetic Map13q32UniSTS
HuRef1373,092,551 - 73,092,743UniSTS
TNG Radiation Hybrid Map1332803.0UniSTS
SHGC-112363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,256,887 - 93,257,171UniSTSGRCh37
Build 361392,054,888 - 92,055,172RGDNCBI36
Celera1374,104,142 - 74,104,426RGD
Cytogenetic Map13q32UniSTS
HuRef1373,853,419 - 73,853,703UniSTS
TNG Radiation Hybrid Map1333326.0UniSTS
SHGC-81110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,238,553 - 93,238,870UniSTSGRCh37
Build 361392,036,554 - 92,036,871RGDNCBI36
Celera1374,085,813 - 74,086,130RGD
Cytogenetic Map13q32UniSTS
HuRef1373,835,090 - 73,835,407UniSTS
TNG Radiation Hybrid Map1333298.0UniSTS
PMC140024P17  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,051,214 - 92,051,623UniSTSGRCh37
Build 361390,849,215 - 90,849,624RGDNCBI36
Celera1372,898,145 - 72,898,554RGD
Cytogenetic Map13q32UniSTS
HuRef1372,646,981 - 72,647,390UniSTS
PMC140024P18  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,100,926 - 92,101,380UniSTSGRCh37
Build 361390,898,927 - 90,899,381RGDNCBI36
Celera1372,947,850 - 72,948,304RGD
Cytogenetic Map13q32UniSTS
HuRef1372,696,774 - 72,697,228UniSTS
PMC140024P19  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,345,376 - 92,346,172UniSTSGRCh37
Build 361391,143,377 - 91,144,173RGDNCBI36
Celera1373,192,581 - 73,193,377RGD
Cytogenetic Map13q32UniSTS
HuRef1372,941,910 - 72,942,706UniSTS
PMC140024P20  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,380,557 - 92,380,964UniSTSGRCh37
Build 361391,178,558 - 91,178,965RGDNCBI36
Celera1373,227,747 - 73,228,154RGD
Cytogenetic Map13q32UniSTS
HuRef1372,977,068 - 72,977,475UniSTS
PMC140024P21  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,408,491 - 92,408,841UniSTSGRCh37
Build 361391,206,492 - 91,206,842RGDNCBI36
Celera1373,255,697 - 73,256,047RGD
Cytogenetic Map13q32UniSTS
HuRef1373,005,016 - 73,005,366UniSTS
PMC140024P23  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,796,899 - 92,797,364UniSTSGRCh37
Build 361391,594,900 - 91,595,365RGDNCBI36
Celera1373,644,149 - 73,644,614RGD
Cytogenetic Map13q32UniSTS
HuRef1373,393,603 - 73,394,068UniSTS
SHGC-52670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,983,764 - 92,983,978UniSTSGRCh37
Build 361391,781,765 - 91,781,979RGDNCBI36
Celera1373,831,020 - 73,831,233RGD
Cytogenetic Map13q32UniSTS
HuRef1373,580,523 - 73,580,736UniSTS
TNG Radiation Hybrid Map1333114.0UniSTS
D13S140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,549,566 - 92,549,689UniSTSGRCh37
Build 361391,347,567 - 91,347,690RGDNCBI36
Celera1373,396,761 - 73,396,886RGD
Cytogenetic Map13q32UniSTS
HuRef1373,146,229 - 73,146,354UniSTS
D13S899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,908,875 - 92,909,054UniSTSGRCh37
Build 361391,706,876 - 91,707,055RGDNCBI36
Celera1373,756,131 - 73,756,310RGD
Cytogenetic Map13q32UniSTS
HuRef1373,505,638 - 73,505,817UniSTS
Whitehead-RH Map13236.3UniSTS
Whitehead-YAC Contig Map13 UniSTS
D13S1490  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,146,546 - 92,146,725UniSTSGRCh37
Build 361390,944,547 - 90,944,726RGDNCBI36
Celera1372,993,496 - 72,993,672RGD
Cytogenetic Map13q32UniSTS
HuRef1372,742,417 - 72,742,593UniSTS
G29145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,229,002 - 92,229,150UniSTSGRCh37
Build 361391,027,003 - 91,027,151RGDNCBI36
Celera1373,075,944 - 73,076,092RGD
Cytogenetic Map13q32UniSTS
HuRef1372,825,622 - 72,825,770UniSTS
D13S1642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,413,313 - 93,413,475UniSTSGRCh37
Build 361392,211,314 - 92,211,476RGDNCBI36
Celera1374,260,553 - 74,260,715RGD
HuRef1374,009,821 - 74,009,983UniSTS
D13S1732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,468,655 - 93,468,890UniSTSGRCh37
Build 361392,266,656 - 92,266,891RGDNCBI36
Celera1374,315,899 - 74,316,134RGD
HuRef1374,065,171 - 74,065,406UniSTS
SHGC-4700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,422,692 - 93,422,880UniSTSGRCh37
Build 361392,220,693 - 92,220,881RGDNCBI36
Celera1374,269,932 - 74,270,120RGD
Cytogenetic Map13q32UniSTS
HuRef1374,019,200 - 74,019,388UniSTS
Stanford-G3 RH Map132643.0UniSTS
NCBI RH Map13857.1UniSTS
G09432  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,573,948 - 92,574,123UniSTSGRCh37
Build 361391,371,949 - 91,372,124RGDNCBI36
Celera1373,421,174 - 73,421,345RGD
Cytogenetic Map13q32UniSTS
HuRef1373,170,509 - 73,170,680UniSTS
RH65549  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,101,139 - 93,101,292UniSTSGRCh37
Build 361391,899,140 - 91,899,293RGDNCBI36
Celera1373,948,176 - 73,948,329RGD
Cytogenetic Map13q32UniSTS
HuRef1373,697,532 - 73,697,685UniSTS
GeneMap99-GB4 RH Map13262.39UniSTS
SHGC-32622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,138,958 - 92,139,107UniSTSGRCh37
Build 361390,936,959 - 90,937,108RGDNCBI36
Celera1372,985,908 - 72,986,057RGD
Cytogenetic Map13q32UniSTS
HuRef1372,734,829 - 72,734,978UniSTS
GeneMap99-GB4 RH Map13257.27UniSTS
Whitehead-RH Map13233.1UniSTS
NCBI RH Map13820.2UniSTS
GeneMap99-G3 RH Map132874.0UniSTS
SHGC-37261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,022,631 - 93,022,758UniSTSGRCh37
Build 361391,820,632 - 91,820,759RGDNCBI36
Celera1373,869,708 - 73,869,835RGD
Cytogenetic Map13q32UniSTS
HuRef1373,619,383 - 73,619,510UniSTS
TNG Radiation Hybrid Map1333126.0UniSTS
Stanford-G3 RH Map132628.0UniSTS
NCBI RH Map13852.8UniSTS
GeneMap99-G3 RH Map132927.0UniSTS
SHGC-12990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,574,256 - 92,574,442UniSTSGRCh37
Build 361391,372,257 - 91,372,443RGDNCBI36
Celera1373,421,478 - 73,421,664RGD
Cytogenetic Map13q32UniSTS
HuRef1373,170,813 - 73,170,999UniSTS
D13S1669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,424,073 - 93,424,196UniSTSGRCh37
Build 361392,222,074 - 92,222,197RGDNCBI36
Celera1374,271,313 - 74,271,436RGD
Cytogenetic Map13q32UniSTS
HuRef1374,020,581 - 74,020,704UniSTS
D10S2412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,864,120 - 92,864,266UniSTSGRCh37
Build 361391,662,121 - 91,662,267RGDNCBI36
Celera1373,711,371 - 73,711,517RGD
Cytogenetic Map13q32UniSTS
HuRef1373,460,822 - 73,460,968UniSTS
A009W27  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,815,411 - 92,815,517UniSTSGRCh37
Build 361391,613,412 - 91,613,518RGDNCBI36
Celera1373,662,670 - 73,662,776RGD
Cytogenetic Map13q32UniSTS
HuRef1373,412,126 - 73,412,232UniSTS
GeneMap99-GB4 RH Map13258.96UniSTS
NCBI RH Map13822.8UniSTS
UniSTS:61556  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371534,774,968 - 34,775,084UniSTSGRCh37
GRCh371393,321,611 - 93,321,712UniSTSGRCh37
Build 361392,119,612 - 92,119,713RGDNCBI36
Celera1374,168,852 - 74,168,953RGD
Celera1511,583,746 - 11,583,864UniSTS
HuRef1511,642,307 - 11,642,425UniSTS
D13S907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,205,968 - 93,206,131UniSTSGRCh37
Build 361392,003,969 - 92,004,132RGDNCBI36
Celera1374,053,214 - 74,053,377RGD
Cytogenetic Map13q32UniSTS
HuRef1373,802,513 - 73,802,676UniSTS
Whitehead-RH Map13246.6UniSTS
Whitehead-YAC Contig Map13 UniSTS
NCBI RH Map13824.2UniSTS
STS-T98842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371393,139,832 - 93,140,007UniSTSGRCh37
Build 361391,937,833 - 91,938,008RGDNCBI36
Celera1373,986,871 - 73,987,046RGD
Cytogenetic Map13q32UniSTS
HuRef1373,736,222 - 73,736,397UniSTS
GeneMap99-GB4 RH Map13262.39UniSTS
G32919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,815,411 - 92,815,517UniSTSGRCh37
Celera1373,662,670 - 73,662,776UniSTS
Cytogenetic Map13q32UniSTS
HuRef1373,412,126 - 73,412,232UniSTS
G54646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,840,731 - 92,840,862UniSTSGRCh37
Celera1373,687,990 - 73,688,121UniSTS
Cytogenetic Map13q32UniSTS
HuRef1373,437,444 - 73,437,575UniSTS
D13S1811  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map13q32UniSTS
HuRef1374,111,220 - 74,111,469UniSTS
Marshfield Genetic Map1372.05UniSTS
Stanford-G3 RH Map132649.0UniSTS
Whitehead-RH Map13249.9UniSTS
NCBI RH Map13859.0UniSTS
RH77946  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map13q32UniSTS
HuRef1373,490,505 - 73,490,626UniSTS
GeneMap99-GB4 RH Map13258.96UniSTS
SHGC-152222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371392,611,248 - 92,611,348UniSTSGRCh37
GRCh371392,611,248 - 92,611,334UniSTSGRCh37
Celera1373,458,492 - 73,458,578UniSTS
Celera1373,458,492 - 73,458,592UniSTS
Cytogenetic Map13q32UniSTS
HuRef1373,207,815 - 73,207,925UniSTS
HuRef1373,207,815 - 73,207,915UniSTS
TNG Radiation Hybrid Map225072.0UniSTS


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
888 2073 2240 2195 4651 1625 2186 2 561 1346 421 1863 5901 5353 32 3710 1 687 1565 1509 146 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_009370 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_004466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017020435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017020436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017020437 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047430153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374222 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374223 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374226 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374227 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374228 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374230 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054374231 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF001462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL138714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL157363 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL157768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL157815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL157821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL159152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL162456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL163537 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL354871 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL356118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL356737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL596221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC030584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC039730 (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
  DB100549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY017486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U66033 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000377067   ⟹   ENSP00000366267
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1391,398,621 - 92,867,237 (+)Ensembl
Ensembl Acc Id: ENST00000483422
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1391,725,058 - 91,756,439 (+)Ensembl
Ensembl Acc Id: ENST00000618283   ⟹   ENSP00000480653
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1392,866,282 - 92,873,682 (+)Ensembl
Ensembl Acc Id: ENST00000618596   ⟹   ENSP00000480819
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1391,693,186 - 91,756,424 (+)Ensembl
RefSeq Acc Id: NM_004466   ⟹   NP_004457
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 92,867,237 (+)NCBI
GRCh371392,050,935 - 93,519,490 (+)ENTREZGENE
Build 361390,848,930 - 92,317,491 (+)NCBI Archive
HuRef1372,646,702 - 74,116,008 (+)ENTREZGENE
CHM1_11392,019,488 - 93,489,120 (+)NCBI
T2T-CHM13v2.01390,601,154 - 92,070,908 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011521054   ⟹   XP_011519356
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 92,016,714 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011521055   ⟹   XP_011519357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 91,768,792 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011521056   ⟹   XP_011519358
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 91,768,792 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011521057   ⟹   XP_011519359
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 91,768,792 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011521058   ⟹   XP_011519360
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 91,824,995 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011521059   ⟹   XP_011519361
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 91,826,798 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011521060   ⟹   XP_011519362
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 91,824,995 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017020435   ⟹   XP_016875924
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 92,751,233 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017020436   ⟹   XP_016875925
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 91,768,792 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017020437   ⟹   XP_016875926
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 91,908,004 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047430153   ⟹   XP_047286109
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,621 - 91,756,364 (+)NCBI
RefSeq Acc Id: XM_054374222   ⟹   XP_054230197
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 91,954,896 (+)NCBI
RefSeq Acc Id: XM_054374223   ⟹   XP_054230198
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 91,219,846 (+)NCBI
RefSeq Acc Id: XM_054374224   ⟹   XP_054230199
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 90,985,742 (+)NCBI
RefSeq Acc Id: XM_054374225   ⟹   XP_054230200
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 90,985,742 (+)NCBI
RefSeq Acc Id: XM_054374226   ⟹   XP_054230201
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 90,985,742 (+)NCBI
RefSeq Acc Id: XM_054374227   ⟹   XP_054230202
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 91,028,250 (+)NCBI
RefSeq Acc Id: XM_054374228   ⟹   XP_054230203
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 91,111,071 (+)NCBI
RefSeq Acc Id: XM_054374229   ⟹   XP_054230204
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 91,028,545 (+)NCBI
RefSeq Acc Id: XM_054374230   ⟹   XP_054230205
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 91,028,250 (+)NCBI
RefSeq Acc Id: XM_054374231   ⟹   XP_054230206
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01390,601,154 - 90,959,098 (+)NCBI
Protein Sequences
Protein RefSeqs NP_004457 (Get FASTA)   NCBI Sequence Viewer  
  XP_011519356 (Get FASTA)   NCBI Sequence Viewer  
  XP_011519357 (Get FASTA)   NCBI Sequence Viewer  
  XP_011519358 (Get FASTA)   NCBI Sequence Viewer  
  XP_011519359 (Get FASTA)   NCBI Sequence Viewer  
  XP_011519360 (Get FASTA)   NCBI Sequence Viewer  
  XP_011519361 (Get FASTA)   NCBI Sequence Viewer  
  XP_011519362 (Get FASTA)   NCBI Sequence Viewer  
  XP_016875924 (Get FASTA)   NCBI Sequence Viewer  
  XP_016875925 (Get FASTA)   NCBI Sequence Viewer  
  XP_016875926 (Get FASTA)   NCBI Sequence Viewer  
  XP_047286109 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230197 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230198 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230199 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230200 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230201 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230202 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230203 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230204 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230205 (Get FASTA)   NCBI Sequence Viewer  
  XP_054230206 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC12261 (Get FASTA)   NCBI Sequence Viewer  
  AAC51118 (Get FASTA)   NCBI Sequence Viewer  
  AAH39730 (Get FASTA)   NCBI Sequence Viewer  
  BAG35673 (Get FASTA)   NCBI Sequence Viewer  
  EAX08927 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000366267
  ENSP00000366267.3
GenBank Protein P78333 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_004457   ⟸   NM_004466
- Peptide Label: precursor
- UniProtKB: O60436 (UniProtKB/Swiss-Prot),   B2R726 (UniProtKB/Swiss-Prot),   Q9BX27 (UniProtKB/Swiss-Prot),   P78333 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011519356   ⟸   XM_011521054
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011519361   ⟸   XM_011521059
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011519360   ⟸   XM_011521058
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011519362   ⟸   XM_011521060
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011519357   ⟸   XM_011521055
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011519358   ⟸   XM_011521056
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011519359   ⟸   XM_011521057
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016875924   ⟸   XM_017020435
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016875926   ⟸   XM_017020437
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016875925   ⟸   XM_017020436
- Peptide Label: isoform X3
- Sequence:
Ensembl Acc Id: ENSP00000366267   ⟸   ENST00000377067
Ensembl Acc Id: ENSP00000480653   ⟸   ENST00000618283
Ensembl Acc Id: ENSP00000480819   ⟸   ENST00000618596
RefSeq Acc Id: XP_047286109   ⟸   XM_047430153
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054230197   ⟸   XM_054374222
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054230198   ⟸   XM_054374223
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054230203   ⟸   XM_054374228
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054230204   ⟸   XM_054374229
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054230202   ⟸   XM_054374227
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054230205   ⟸   XM_054374230
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054230199   ⟸   XM_054374224
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054230200   ⟸   XM_054374225
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054230201   ⟸   XM_054374226
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054230206   ⟸   XM_054374231
- Peptide Label: isoform X5

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P78333-F1-model_v2 AlphaFold P78333 1-572 view protein structure

Promoters
RGD ID:6790891
Promoter ID:HG_KWN:18254
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:OTTHUMT00000045454,   UC001VLS.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361390,848,654 - 90,849,154 (+)MPROMDB
RGD ID:7226643
Promoter ID:EPDNEW_H19067
Type:initiation region
Name:GPC5_1
Description:glypican 5
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381391,398,631 - 91,398,691EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:4453 AgrOrtholog
COSMIC GPC5 COSMIC
Ensembl Genes ENSG00000179399 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000377067 ENTREZGENE
  ENST00000377067.9 UniProtKB/Swiss-Prot
GTEx ENSG00000179399 GTEx
HGNC ID HGNC:4453 ENTREZGENE
Human Proteome Map GPC5 Human Proteome Map
InterPro Glypican UniProtKB/Swiss-Prot
  Glypican_CS UniProtKB/Swiss-Prot
KEGG Report hsa:2262 UniProtKB/Swiss-Prot
NCBI Gene 2262 ENTREZGENE
OMIM 602446 OMIM
PANTHER PTHR10822 UniProtKB/Swiss-Prot
  PTHR10822:SF12 UniProtKB/Swiss-Prot
Pfam Glypican UniProtKB/Swiss-Prot
PharmGKB PA28834 PharmGKB
PROSITE GLYPICAN UniProtKB/Swiss-Prot
UniProt A0A087WX13_HUMAN UniProtKB/TrEMBL
  B2R726 ENTREZGENE
  GPC5_HUMAN UniProtKB/Swiss-Prot
  O60436 ENTREZGENE
  P78333 ENTREZGENE
  Q9BX27 ENTREZGENE
UniProt Secondary B2R726 UniProtKB/Swiss-Prot
  O60436 UniProtKB/Swiss-Prot
  Q9BX27 UniProtKB/Swiss-Prot