PCDHA9 (protocadherin alpha 9) - Rat Genome Database

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Gene: PCDHA9 (protocadherin alpha 9) Homo sapiens
Analyze
Symbol: PCDHA9
Name: protocadherin alpha 9
RGD ID: 1343466
HGNC Page HGNC:8675
Description: Predicted to enable calcium ion binding activity. Predicted to be involved in cell adhesion. Predicted to be located in plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: KIAA0345; KIAA0345-like 5; PCDH-alpha-9; PCDH-ALPHA9; protocadherin alpha-9
RGD Orthologs
Mouse
Rat
Bonobo
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385140,847,772 - 141,012,347 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5140,847,772 - 141,012,347 (+)EnsemblGRCh38hg38GRCh38
GRCh375140,227,357 - 140,391,932 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365140,207,541 - 140,372,113 (+)NCBINCBI36Build 36hg18NCBI36
Build 345140,207,540 - 140,372,113NCBI
Celera5136,304,162 - 136,468,708 (+)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,372,092 - 135,536,628 (+)NCBIHuRef
CHM1_15139,660,543 - 139,825,092 (+)NCBICHM1_1
T2T-CHM13v2.05141,373,097 - 141,537,634 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. 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
Additional References at PubMed
PMID:9205841   PMID:10380929   PMID:10662547   PMID:10716726   PMID:10817752   PMID:10835267   PMID:11230163   PMID:12477932   PMID:15372022   PMID:15489334   PMID:17474147   PMID:21873635  
PMID:22589738   PMID:28514442   PMID:28625976   PMID:29477871   PMID:33961781  


Genomics

Comparative Map Data
PCDHA9
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385140,847,772 - 141,012,347 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5140,847,772 - 141,012,347 (+)EnsemblGRCh38hg38GRCh38
GRCh375140,227,357 - 140,391,932 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365140,207,541 - 140,372,113 (+)NCBINCBI36Build 36hg18NCBI36
Build 345140,207,540 - 140,372,113NCBI
Celera5136,304,162 - 136,468,708 (+)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,372,092 - 135,536,628 (+)NCBIHuRef
CHM1_15139,660,543 - 139,825,092 (+)NCBICHM1_1
T2T-CHM13v2.05141,373,097 - 141,537,634 (+)NCBIT2T-CHM13v2.0
Pcdha8
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391837,125,520 - 37,320,710 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1837,125,424 - 37,320,710 (+)EnsemblGRCm39 Ensembl
GRCm381836,992,467 - 37,187,657 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1836,992,371 - 37,187,657 (+)EnsemblGRCm38mm10GRCm38
MGSCv371837,152,121 - 37,347,311 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361837,118,441 - 37,313,631 (+)NCBIMGSCv36mm8
Celera1837,439,238 - 37,441,618 (+)NCBICelera
Cytogenetic Map18B2- B3NCBI
cM Map1819.46NCBI
Pcdha9
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.01830,004,565 - 30,215,897 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1829,987,206 - 30,215,897 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01829,701,815 - 29,924,444 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41829,715,235 - 29,928,031 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11829,741,880 - 29,954,676 (+)NCBI
Celera1828,343,398 - 28,552,755 (+)NCBICelera
Cytogenetic Map18p11NCBI
LOC100992160
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v24136,039,789 - 136,269,711 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan15134,179,338 - 134,408,495 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v05136,150,262 - 136,376,530 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.15142,280,506 - 142,491,362 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl5142,321,070 - 142,488,986 (+)Ensemblpanpan1.1panPan2

Variants

.
Variants in PCDHA9
293 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3 copy number gain See cases [RCV000051193] Chr5:130860928..155321811 [GRCh38]
Chr5:130196621..154701371 [GRCh37]
Chr5:130224520..154681564 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-32(chr5:138871137-145812309)x1 copy number loss See cases [RCV000052142] Chr5:138871137..145812309 [GRCh38]
Chr5:138206826..145191872 [GRCh37]
Chr5:138234725..145172065 [NCBI36]
Chr5:5q31.2-32
pathogenic
GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1 copy number loss See cases [RCV000053524] Chr5:106619588..156124387 [GRCh38]
Chr5:105955289..155551397 [GRCh37]
Chr5:105983188..155483975 [NCBI36]
Chr5:5q21.3-33.2
pathogenic
NM_031857.1(PCDHA9):c.449C>T (p.Ser150Phe) single nucleotide variant Malignant melanoma [RCV000066681] Chr5:140848944 [GRCh38]
Chr5:140228529 [GRCh37]
Chr5:140208713 [NCBI36]
Chr5:5q31.3
not provided
NM_031857.1(PCDHA9):c.906C>T (p.Ile302=) single nucleotide variant Malignant melanoma [RCV000061136] Chr5:140849401 [GRCh38]
Chr5:140228986 [GRCh37]
Chr5:140209170 [NCBI36]
Chr5:5q31.3
not provided
NM_018901.3(PCDHA10):c.803C>T (p.Ser268Leu) single nucleotide variant Malignant melanoma [RCV000061137] Chr5:140856851 [GRCh38]
Chr5:140236436 [GRCh37]
Chr5:140216620 [NCBI36]
Chr5:5q31.3
not provided
NM_018904.2(PCDHA13):c.1372C>T (p.Pro458Ser) single nucleotide variant Malignant melanoma [RCV000061138] Chr5:140883640 [GRCh38]
Chr5:140263225 [GRCh37]
Chr5:140243409 [NCBI36]
Chr5:5q31.3
not provided
NM_018898.3(PCDHAC1):c.1559G>C (p.Gly520Ala) single nucleotide variant Malignant melanoma [RCV000061139] Chr5:140928451 [GRCh38]
Chr5:140308036 [GRCh37]
Chr5:140288220 [NCBI36]
Chr5:5q31.3
not provided
NM_018898.3(PCDHAC1):c.1672C>T (p.Pro558Ser) single nucleotide variant Malignant melanoma [RCV000061140] Chr5:140928564 [GRCh38]
Chr5:140308149 [GRCh37]
Chr5:140288333 [NCBI36]
Chr5:5q31.3
not provided
NM_018899.5(PCDHAC2):c.1957G>A (p.Gly653Ser) single nucleotide variant Malignant melanoma [RCV000061141] Chr5:140968723 [GRCh38]
Chr5:140348308 [GRCh37]
Chr5:140328492 [NCBI36]
Chr5:5q31.3
not provided
NM_018898.3(PCDHAC1):c.2742G>A (p.Gln914=) single nucleotide variant Malignant melanoma [RCV000061142] Chr5:141009787 [GRCh38]
Chr5:140389372 [GRCh37]
Chr5:140369556 [NCBI36]
Chr5:5q31.3
not provided
NM_018911.2(PCDHA8):c.1599C>T (p.Phe533=) single nucleotide variant Malignant melanoma [RCV000066680] Chr5:140842920 [GRCh38]
Chr5:140222505 [GRCh37]
Chr5:140202689 [NCBI36]
Chr5:5q31.3
not provided
NM_031857.1(PCDHA9):c.1405C>A (p.Pro469Thr) single nucleotide variant Malignant melanoma [RCV000066682] Chr5:140849900 [GRCh38]
Chr5:140229485 [GRCh37]
Chr5:140209669 [NCBI36]
Chr5:5q31.3
not provided
NM_018901.3(PCDHA10):c.845C>T (p.Ser282Phe) single nucleotide variant Malignant melanoma [RCV000066683] Chr5:140856893 [GRCh38]
Chr5:140236478 [GRCh37]
Chr5:140216662 [NCBI36]
Chr5:5q31.3
not provided
NM_018901.3(PCDHA10):c.2070C>T (p.Ala690=) single nucleotide variant Malignant melanoma [RCV000066684] Chr5:140858118 [GRCh38]
Chr5:140237703 [GRCh37]
Chr5:140217887 [NCBI36]
Chr5:5q31.3
not provided
NM_018903.3(PCDHA12):c.955C>T (p.Gln319Ter) single nucleotide variant Malignant melanoma [RCV000066685] Chr5:140876427 [GRCh38]
Chr5:140256012 [GRCh37]
Chr5:140236196 [NCBI36]
Chr5:5q31.3
not provided
NM_018903.3(PCDHA12):c.2083G>A (p.Asp695Asn) single nucleotide variant Malignant melanoma [RCV000066686] Chr5:140877555 [GRCh38]
Chr5:140257140 [GRCh37]
Chr5:140237324 [NCBI36]
Chr5:5q31.3
not provided
NM_018904.2(PCDHA13):c.693G>A (p.Thr231=) single nucleotide variant Malignant melanoma [RCV000066687] Chr5:140882961 [GRCh38]
Chr5:140262546 [GRCh37]
Chr5:140242730 [NCBI36]
Chr5:5q31.3
not provided
NM_018904.2(PCDHA13):c.815G>A (p.Gly272Asp) single nucleotide variant Malignant melanoma [RCV000066688] Chr5:140883083 [GRCh38]
Chr5:140262668 [GRCh37]
Chr5:140242852 [NCBI36]
Chr5:5q31.3
not provided
NM_018904.2(PCDHA13):c.977G>A (p.Gly326Glu) single nucleotide variant Malignant melanoma [RCV000066689] Chr5:140883245 [GRCh38]
Chr5:140262830 [GRCh37]
Chr5:140243014 [NCBI36]
Chr5:5q31.3
not provided
NM_018898.3(PCDHAC1):c.1688G>A (p.Gly563Asp) single nucleotide variant Malignant melanoma [RCV000066691] Chr5:140928580 [GRCh38]
Chr5:140308165 [GRCh37]
Chr5:140288349 [NCBI36]
Chr5:5q31.3
not provided
NM_018899.5(PCDHAC2):c.589C>T (p.Leu197Phe) single nucleotide variant Malignant melanoma [RCV000066692] Chr5:140967355 [GRCh38]
Chr5:140346940 [GRCh37]
Chr5:140327124 [NCBI36]
Chr5:5q31.3
not provided
NM_018899.5(PCDHAC2):c.703C>T (p.Pro235Ser) single nucleotide variant Malignant melanoma [RCV000066693] Chr5:140967469 [GRCh38]
Chr5:140347054 [GRCh37]
Chr5:140327238 [NCBI36]
Chr5:5q31.3
not provided
NM_018899.5(PCDHAC2):c.2248G>A (p.Glu750Lys) single nucleotide variant Malignant melanoma [RCV000066694] Chr5:140969014 [GRCh38]
Chr5:140348599 [GRCh37]
Chr5:140328783 [NCBI36]
Chr5:5q31.3
not provided
NM_018898.3(PCDHAC1):c.1359C>T (p.Phe453=) single nucleotide variant Malignant melanoma [RCV000066690] Chr5:140928251 [GRCh38]
Chr5:140307836 [GRCh37]
Chr5:140288020 [NCBI36]
Chr5:5q31.3
not provided
NM_018898.5(PCDHAC1):c.2396G>A (p.Arg799Gln) single nucleotide variant not provided [RCV000122558] Chr5:140929288 [GRCh38]
Chr5:140308873 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1166C>T (p.Thr389Met) single nucleotide variant Malignant tumor of prostate [RCV000149260] Chr5:140857214 [GRCh38]
Chr5:140236799 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh38/hg38 5q31.3(chr5:140963199-142322798)x1 copy number loss See cases [RCV000136949] Chr5:140963199..142322798 [GRCh38]
Chr5:140453735..141702363 [GRCh37]
Chr5:140322968..141682547 [NCBI36]
Chr5:5q31.3
uncertain significance
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3 copy number gain See cases [RCV000138808] Chr5:129847794..153353546 [GRCh38]
Chr5:129183487..152733106 [GRCh37]
Chr5:129211386..152713299 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-31.3(chr5:138942857-144605017)x3 copy number gain See cases [RCV000142806] Chr5:138942857..144605017 [GRCh38]
Chr5:138278546..143984580 [GRCh37]
Chr5:138306445..143964773 [NCBI36]
Chr5:5q31.2-31.3
uncertain significance
NM_031857.2(PCDHA9):c.1937G>T (p.Arg646Leu) single nucleotide variant Inborn genetic diseases [RCV003246571] Chr5:140850432 [GRCh38]
Chr5:140230017 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 copy number gain not provided [RCV000487658] Chr5:94844077..178830410 [GRCh37]
Chr5:5q15-35.3
likely benign
NC_000005.9:g.(?_86400000)_(154000000_?)del deletion Familial adenomatous polyposis 1 [RCV002231249]|Hereditary cancer-predisposing syndrome [RCV000554476] Chr5:86400000..154000000 [GRCh37]
Chr5:5q14.3-33.2
pathogenic
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 copy number gain See cases [RCV000449349] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
NM_018901.4(PCDHA10):c.897A>T (p.Gly299=) single nucleotide variant not specified [RCV000429816] Chr5:140856945 [GRCh38]
Chr5:140236530 [GRCh37]
Chr5:5q31.3
likely benign
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 copy number gain See cases [RCV000448245] Chr5:106716357..180687338 [GRCh37]
Chr5:5q21.3-35.3
pathogenic
NM_018900.4(PCDHA1):c.2420G>A (p.Arg807His) single nucleotide variant Hirschsprung disease, susceptibility to, 1 [RCV000508600] Chr5:140978974 [GRCh38]
Chr5:140358559 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NM_018904.3(PCDHA13):c.1471T>G (p.Ser491Ala) single nucleotide variant Inborn genetic diseases [RCV003276206] Chr5:140883739 [GRCh38]
Chr5:140263324 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1337C>G (p.Ala446Gly) single nucleotide variant Inborn genetic diseases [RCV003255685] Chr5:140883605 [GRCh38]
Chr5:140263190 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1553A>T (p.Tyr518Phe) single nucleotide variant Inborn genetic diseases [RCV003255732] Chr5:140883821 [GRCh38]
Chr5:140263406 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.128C>A (p.Thr43Asn) single nucleotide variant Inborn genetic diseases [RCV003299136] Chr5:140848623 [GRCh38]
Chr5:140228208 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.968A>G (p.Asp323Gly) single nucleotide variant Inborn genetic diseases [RCV003293573] Chr5:140870071 [GRCh38]
Chr5:140249656 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.212A>G (p.His71Arg) single nucleotide variant Inborn genetic diseases [RCV003276204] Chr5:140875684 [GRCh38]
Chr5:140255269 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.1942G>C (p.Val648Leu) single nucleotide variant Inborn genetic diseases [RCV003287280] Chr5:140857990 [GRCh38]
Chr5:140237575 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.2048C>G (p.Ser683Trp) single nucleotide variant Inborn genetic diseases [RCV003287281] Chr5:140884316 [GRCh38]
Chr5:140263901 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.337C>G (p.Pro113Ala) single nucleotide variant Inborn genetic diseases [RCV003263282] Chr5:140848832 [GRCh38]
Chr5:140228417 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1256C>T (p.Ala419Val) single nucleotide variant Inborn genetic diseases [RCV003257182] Chr5:140857304 [GRCh38]
Chr5:140236889 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1255T>G (p.Ser419Ala) single nucleotide variant Inborn genetic diseases [RCV003288832] Chr5:140883523 [GRCh38]
Chr5:140263108 [GRCh37]
Chr5:5q31.3
likely benign
NM_018904.3(PCDHA13):c.1331G>A (p.Gly444Glu) single nucleotide variant Inborn genetic diseases [RCV003288833] Chr5:140883599 [GRCh38]
Chr5:140263184 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.1505A>G (p.His502Arg) single nucleotide variant Inborn genetic diseases [RCV003255726] Chr5:140876977 [GRCh38]
Chr5:140256562 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.208A>G (p.Arg70Gly) single nucleotide variant Inborn genetic diseases [RCV003255728] Chr5:140875680 [GRCh38]
Chr5:140255265 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.211C>G (p.His71Asp) single nucleotide variant Inborn genetic diseases [RCV003255729] Chr5:140875683 [GRCh38]
Chr5:140255268 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.128C>A (p.Thr43Asn) single nucleotide variant Inborn genetic diseases [RCV003254625] Chr5:140882396 [GRCh38]
Chr5:140261981 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.344A>C (p.Gln115Pro) single nucleotide variant Inborn genetic diseases [RCV003272570] Chr5:140875816 [GRCh38]
Chr5:140255401 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1463T>G (p.Leu488Arg) single nucleotide variant Inborn genetic diseases [RCV003276199] Chr5:140870566 [GRCh38]
Chr5:140250151 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1372C>A (p.Pro458Thr) single nucleotide variant Inborn genetic diseases [RCV003296320] Chr5:140876844 [GRCh38]
Chr5:140256429 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q31.2-31.3(chr5:139147238-141540491)x1 copy number loss not provided [RCV000682600] Chr5:139147238..141540491 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5q31.3(chr5:140181892-140303139)x3 copy number gain not provided [RCV000745213] Chr5:140181892..140303139 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140212676-140228164)x1 copy number loss not provided [RCV000745214] Chr5:140212676..140228164 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140215845-140227876)x1 copy number loss not provided [RCV000745215] Chr5:140215845..140227876 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140215845-140228164)x1 copy number loss not provided [RCV000745216] Chr5:140215845..140228164 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140215845-140244335)x1 copy number loss not provided [RCV000745217] Chr5:140215845..140244335 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140222641-140244335)x1 copy number loss not provided [RCV000745218] Chr5:140222641..140244335 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140223666-140244335)x0 copy number loss not provided [RCV000745219] Chr5:140223666..140244335 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140228262-140264271)x3 copy number gain not provided [RCV000745220] Chr5:140228262..140264271 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140229435-140261235)x3 copy number gain not provided [RCV000745221] Chr5:140229435..140261235 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140244335-140282431)x1 copy number loss not provided [RCV000745222] Chr5:140244335..140282431 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140266429-140298815)x0 copy number loss not provided [RCV000745223] Chr5:140266429..140298815 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140101612-140271424)x3 copy number gain not provided [RCV000745200] Chr5:140101612..140271424 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140102539-140347053)x1 copy number loss not provided [RCV000745201] Chr5:140102539..140347053 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140115433-140238694)x1 copy number loss not provided [RCV000745203] Chr5:140115433..140238694 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140162610-140282431)x1 copy number loss not provided [RCV000745207] Chr5:140162610..140282431 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140115433-140264271)x3 copy number gain not provided [RCV000745204] Chr5:140115433..140264271 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140115433-140282431)x1 copy number loss not provided [RCV000745205] Chr5:140115433..140282431 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140115433-140344242)x1 copy number loss not provided [RCV000745206] Chr5:140115433..140344242 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140166534-140271424)x3 copy number gain not provided [RCV000745208] Chr5:140166534..140271424 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140176243-140264271)x3 copy number gain not provided [RCV000745209] Chr5:140176243..140264271 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140176840-140264271)x3 copy number gain not provided [RCV000745210] Chr5:140176840..140264271 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140176842-140264271)x3 copy number gain not provided [RCV000745211] Chr5:140176842..140264271 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140181359-140264271)x3 copy number gain not provided [RCV000745212] Chr5:140181359..140264271 [GRCh37]
Chr5:5q31.3
benign
NM_018903.4(PCDHA12):c.1503G>C (p.Glu501Asp) single nucleotide variant Inborn genetic diseases [RCV003268760] Chr5:140876975 [GRCh38]
Chr5:140256560 [GRCh37]
Chr5:5q31.3
uncertain significance
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32
uncertain significance
NM_031857.2(PCDHA9):c.2406C>G (p.Pro802=) single nucleotide variant not provided [RCV000922554] Chr5:140978960 [GRCh38]
Chr5:140358545 [GRCh37]
Chr5:5q31.3
likely benign
NM_018899.6(PCDHAC2):c.2841C>A (p.Ile947=) single nucleotide variant not provided [RCV000881803] Chr5:141009754 [GRCh38]
Chr5:140389339 [GRCh37]
Chr5:5q31.3
likely benign
NM_018902.5(PCDHA11):c.982C>T (p.Pro328Ser) single nucleotide variant Inborn genetic diseases [RCV003310693] Chr5:140870085 [GRCh38]
Chr5:140249670 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.2492C>G (p.Pro831Arg) single nucleotide variant not provided [RCV000950135] Chr5:140982540 [GRCh38]
Chr5:140362125 [GRCh37]
Chr5:5q31.3
benign|likely benign
NM_018903.4(PCDHA12):c.1546A>C (p.Lys516Gln) single nucleotide variant Inborn genetic diseases [RCV003288827] Chr5:140877018 [GRCh38]
Chr5:140256603 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1574A>G (p.His525Arg) single nucleotide variant Inborn genetic diseases [RCV003288828] Chr5:140877046 [GRCh38]
Chr5:140256631 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1231A>G (p.Ser411Gly) single nucleotide variant Inborn genetic diseases [RCV003288830] Chr5:140883499 [GRCh38]
Chr5:140263084 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.804T>A (p.Asp268Glu) single nucleotide variant Inborn genetic diseases [RCV003272781] Chr5:140883072 [GRCh38]
Chr5:140262657 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1973C>T (p.Ala658Val) single nucleotide variant Inborn genetic diseases [RCV003270703] Chr5:140877445 [GRCh38]
Chr5:140257030 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1601A>G (p.Gln534Arg) single nucleotide variant Inborn genetic diseases [RCV003288829] Chr5:140877073 [GRCh38]
Chr5:140256658 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1439A>G (p.Gln480Arg) single nucleotide variant Inborn genetic diseases [RCV003288834] Chr5:140883707 [GRCh38]
Chr5:140263292 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.1495G>T (p.Val499Leu) single nucleotide variant Inborn genetic diseases [RCV003268759] Chr5:140876967 [GRCh38]
Chr5:140256552 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.380A>G (p.Asp127Gly) single nucleotide variant Inborn genetic diseases [RCV003274529] Chr5:140856428 [GRCh38]
Chr5:140236013 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1208T>A (p.Leu403Gln) single nucleotide variant Inborn genetic diseases [RCV003272794] Chr5:140928100 [GRCh38]
Chr5:140307685 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.703G>A (p.Val235Met) single nucleotide variant not provided [RCV001572857] Chr5:140876175 [GRCh38]
Chr5:140255760 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.1677C>G (p.Asn559Lys) single nucleotide variant Inborn genetic diseases [RCV003275377] Chr5:140877149 [GRCh38]
Chr5:140256734 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1459G>A (p.Val487Ile) single nucleotide variant Inborn genetic diseases [RCV003275468] Chr5:140928351 [GRCh38]
Chr5:140307936 [GRCh37]
Chr5:5q31.3
likely benign
NM_031857.2(PCDHA9):c.1320G>C (p.Arg440Ser) single nucleotide variant Inborn genetic diseases [RCV003241932] Chr5:140849815 [GRCh38]
Chr5:140229400 [GRCh37]
Chr5:5q31.3
likely benign
NM_018904.3(PCDHA13):c.2613C>T (p.Tyr871=) single nucleotide variant not provided [RCV000879250] Chr5:141009697 [GRCh38]
Chr5:140389282 [GRCh37]
Chr5:5q31.3
likely benign
NM_018902.5(PCDHA11):c.1468T>G (p.Ser490Ala) single nucleotide variant Inborn genetic diseases [RCV003276200] Chr5:140870571 [GRCh38]
Chr5:140250156 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1471T>G (p.Ser491Ala) single nucleotide variant Inborn genetic diseases [RCV003276202] Chr5:140876943 [GRCh38]
Chr5:140256528 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.210A>C (p.Arg70Ser) single nucleotide variant Inborn genetic diseases [RCV003276203] Chr5:140875682 [GRCh38]
Chr5:140255267 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.-62_2388+204del deletion Thrombocytosis [RCV001252978] Chr5:140855985..140858638 [GRCh38]
Chr5:140235570..140238223 [GRCh37]
Chr5:5q31.3
uncertain significance
NC_000005.9:g.(?_136633338)_(140998481_?)dup duplication PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001339088] Chr5:136633338..140998481 [GRCh37]
Chr5:5q31.2-31.3
uncertain significance
NM_018907.4(PCDHA4):c.2499T>A (p.Asp833Glu) single nucleotide variant not provided [RCV001454211] Chr5:140982529 [GRCh38]
Chr5:140362114 [GRCh37]
Chr5:5q31.3
likely benign
NM_018900.4(PCDHA1):c.2394+69786T>C single nucleotide variant not provided [RCV001710086] Chr5:140858470 [GRCh38]
Chr5:140238055 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.2-31.3(chr5:139493717-140517454)x1 copy number loss PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001801202] Chr5:139493717..140517454 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910) copy number gain not specified [RCV002053526] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
NM_018902.5(PCDHA11):c.1550A>T (p.Tyr517Phe) single nucleotide variant Inborn genetic diseases [RCV003276201] Chr5:140870653 [GRCh38]
Chr5:140250238 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1444G>C (p.Ala482Pro) single nucleotide variant Inborn genetic diseases [RCV003276367] Chr5:140883712 [GRCh38]
Chr5:140263297 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1613A>G (p.Asp538Gly) single nucleotide variant Inborn genetic diseases [RCV003294749] Chr5:140870716 [GRCh38]
Chr5:140250301 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.299C>T (p.Ala100Val) single nucleotide variant Inborn genetic diseases [RCV003255735] Chr5:140848794 [GRCh38]
Chr5:140228379 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1543A>C (p.Lys515Gln) single nucleotide variant Inborn genetic diseases [RCV003255723] Chr5:140870646 [GRCh38]
Chr5:140250231 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1466T>G (p.Leu489Arg) single nucleotide variant Inborn genetic diseases [RCV003255725] Chr5:140876938 [GRCh38]
Chr5:140256523 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1466T>G (p.Leu489Arg) single nucleotide variant Inborn genetic diseases [RCV003255730] Chr5:140883734 [GRCh38]
Chr5:140263319 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2354G>A (p.Gly785Glu) single nucleotide variant Inborn genetic diseases [RCV003285052] Chr5:140871457 [GRCh38]
Chr5:140251042 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.1553A>T (p.Tyr518Phe) single nucleotide variant Inborn genetic diseases [RCV003302400] Chr5:140877025 [GRCh38]
Chr5:140256610 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1625T>C (p.Val542Ala) single nucleotide variant Inborn genetic diseases [RCV003302401] Chr5:140877097 [GRCh38]
Chr5:140256682 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1234G>A (p.Ala412Thr) single nucleotide variant Inborn genetic diseases [RCV003302402] Chr5:140883502 [GRCh38]
Chr5:140263087 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q31.3(chr5:140082762-140773954)x3 copy number gain not provided [RCV002474614] Chr5:140082762..140773954 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.345G>C (p.Gln115His) single nucleotide variant Inborn genetic diseases [RCV002879902] Chr5:140875817 [GRCh38]
Chr5:140255402 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2280G>C (p.Glu760Asp) single nucleotide variant Inborn genetic diseases [RCV002837022] Chr5:140871383 [GRCh38]
Chr5:140250968 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.361G>A (p.Val121Met) single nucleotide variant Inborn genetic diseases [RCV002817725] Chr5:140875833 [GRCh38]
Chr5:140255418 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1442C>T (p.Ala481Val) single nucleotide variant Inborn genetic diseases [RCV002683581] Chr5:140870545 [GRCh38]
Chr5:140250130 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.701C>T (p.Ala234Val) single nucleotide variant Inborn genetic diseases [RCV002729909] Chr5:140856749 [GRCh38]
Chr5:140236334 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.881A>G (p.Gln294Arg) single nucleotide variant Inborn genetic diseases [RCV002817987] Chr5:140927773 [GRCh38]
Chr5:140307358 [GRCh37]
Chr5:5q31.3
likely benign
NM_031857.2(PCDHA9):c.1001G>A (p.Cys334Tyr) single nucleotide variant Inborn genetic diseases [RCV002818058] Chr5:140849496 [GRCh38]
Chr5:140229081 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.2224A>G (p.Ile742Val) single nucleotide variant Inborn genetic diseases [RCV002906686] Chr5:140929116 [GRCh38]
Chr5:140308701 [GRCh37]
Chr5:5q31.3
likely benign
NM_018898.5(PCDHAC1):c.143C>A (p.Ala48Asp) single nucleotide variant Inborn genetic diseases [RCV002840464] Chr5:140927035 [GRCh38]
Chr5:140306620 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.107A>C (p.Tyr36Ser) single nucleotide variant Inborn genetic diseases [RCV002729367] Chr5:140875579 [GRCh38]
Chr5:140255164 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.1904T>C (p.Val635Ala) single nucleotide variant Inborn genetic diseases [RCV002794292] Chr5:140968670 [GRCh38]
Chr5:140348255 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1522G>A (p.Val508Met) single nucleotide variant Inborn genetic diseases [RCV002864592] Chr5:140883790 [GRCh38]
Chr5:140263375 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.81C>G (p.Ser27Arg) single nucleotide variant Inborn genetic diseases [RCV002794109] Chr5:140856129 [GRCh38]
Chr5:140235714 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1523C>T (p.Ser508Leu) single nucleotide variant Inborn genetic diseases [RCV002778466] Chr5:140870626 [GRCh38]
Chr5:140250211 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1075G>C (p.Val359Leu) single nucleotide variant Inborn genetic diseases [RCV002972705] Chr5:140849570 [GRCh38]
Chr5:140229155 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.516T>G (p.Ser172Arg) single nucleotide variant Inborn genetic diseases [RCV002734247] Chr5:140856564 [GRCh38]
Chr5:140236149 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.106G>T (p.Val36Leu) single nucleotide variant Inborn genetic diseases [RCV002883791] Chr5:140926998 [GRCh38]
Chr5:140306583 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.2038G>T (p.Val680Leu) single nucleotide variant Inborn genetic diseases [RCV002990311] Chr5:140968804 [GRCh38]
Chr5:140348389 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.361G>T (p.Val121Leu) single nucleotide variant Inborn genetic diseases [RCV002969036] Chr5:140875833 [GRCh38]
Chr5:140255418 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.509A>G (p.Tyr170Cys) single nucleotide variant Inborn genetic diseases [RCV002776656] Chr5:140875981 [GRCh38]
Chr5:140255566 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.1387A>G (p.Asn463Asp) single nucleotide variant Inborn genetic diseases [RCV002688427] Chr5:140968153 [GRCh38]
Chr5:140347738 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1864C>T (p.Arg622Cys) single nucleotide variant Inborn genetic diseases [RCV002729341] Chr5:140857912 [GRCh38]
Chr5:140237497 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.2111T>C (p.Ile704Thr) single nucleotide variant Inborn genetic diseases [RCV002728588] Chr5:140968877 [GRCh38]
Chr5:140348462 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2013C>A (p.Ser671Arg) single nucleotide variant Inborn genetic diseases [RCV002970563] Chr5:140871116 [GRCh38]
Chr5:140250701 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.2288G>A (p.Gly763Asp) single nucleotide variant Inborn genetic diseases [RCV002772985] Chr5:140850783 [GRCh38]
Chr5:140230368 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.384C>G (p.Asp128Glu) single nucleotide variant Inborn genetic diseases [RCV002905954] Chr5:140848879 [GRCh38]
Chr5:140228464 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1249G>T (p.Val417Leu) single nucleotide variant Inborn genetic diseases [RCV002773380] Chr5:140870352 [GRCh38]
Chr5:140249937 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1469T>C (p.Val490Ala) single nucleotide variant Inborn genetic diseases [RCV002945944] Chr5:140876941 [GRCh38]
Chr5:140256526 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1636G>A (p.Gly546Ser) single nucleotide variant Inborn genetic diseases [RCV002969949] Chr5:140877108 [GRCh38]
Chr5:140256693 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.38G>T (p.Arg13Leu) single nucleotide variant Inborn genetic diseases [RCV002687877] Chr5:140875510 [GRCh38]
Chr5:140255095 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1688C>A (p.Pro563Gln) single nucleotide variant Inborn genetic diseases [RCV002752181] Chr5:140877160 [GRCh38]
Chr5:140256745 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.125G>A (p.Gly42Asp) single nucleotide variant Inborn genetic diseases [RCV002684592] Chr5:140848620 [GRCh38]
Chr5:140228205 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.320A>G (p.Glu107Gly) single nucleotide variant Inborn genetic diseases [RCV002731836] Chr5:140882588 [GRCh38]
Chr5:140262173 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.179T>C (p.Val60Ala) single nucleotide variant Inborn genetic diseases [RCV002818845] Chr5:140875651 [GRCh38]
Chr5:140255236 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1645G>A (p.Val549Met) single nucleotide variant Inborn genetic diseases [RCV002733033] Chr5:140883913 [GRCh38]
Chr5:140263498 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.682A>G (p.Thr228Ala) single nucleotide variant Inborn genetic diseases [RCV002732033] Chr5:140967448 [GRCh38]
Chr5:140347033 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1517G>A (p.Ser506Asn) single nucleotide variant Inborn genetic diseases [RCV002818951] Chr5:140850012 [GRCh38]
Chr5:140229597 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1261G>A (p.Glu421Lys) single nucleotide variant Inborn genetic diseases [RCV002946695] Chr5:140870364 [GRCh38]
Chr5:140249949 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.545T>C (p.Ile182Thr) single nucleotide variant Inborn genetic diseases [RCV002818245] Chr5:140876017 [GRCh38]
Chr5:140255602 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.996C>A (p.His332Gln) single nucleotide variant Inborn genetic diseases [RCV002864911] Chr5:140870099 [GRCh38]
Chr5:140249684 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.275A>G (p.Glu92Gly) single nucleotide variant Inborn genetic diseases [RCV002818435] Chr5:140856323 [GRCh38]
Chr5:140235908 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1127A>C (p.His376Pro) single nucleotide variant Inborn genetic diseases [RCV002739628] Chr5:140857175 [GRCh38]
Chr5:140236760 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.91C>T (p.His31Tyr) single nucleotide variant Inborn genetic diseases [RCV002762476] Chr5:140856139 [GRCh38]
Chr5:140235724 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.436G>A (p.Ala146Thr) single nucleotide variant Inborn genetic diseases [RCV002737104] Chr5:140875908 [GRCh38]
Chr5:140255493 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1204C>A (p.Pro402Thr) single nucleotide variant Inborn genetic diseases [RCV002849180] Chr5:140928096 [GRCh38]
Chr5:140307681 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.811C>T (p.Pro271Ser) single nucleotide variant Inborn genetic diseases [RCV002737973] Chr5:140967577 [GRCh38]
Chr5:140347162 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1444G>T (p.Ala482Ser) single nucleotide variant Inborn genetic diseases [RCV002799194] Chr5:140849939 [GRCh38]
Chr5:140229524 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.172G>C (p.Glu58Gln) single nucleotide variant Inborn genetic diseases [RCV002888065] Chr5:140848667 [GRCh38]
Chr5:140228252 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.106T>C (p.Tyr36His) single nucleotide variant Inborn genetic diseases [RCV002821881] Chr5:140875578 [GRCh38]
Chr5:140255163 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.2111T>C (p.Ile704Thr) single nucleotide variant Inborn genetic diseases [RCV002849337] Chr5:140877583 [GRCh38]
Chr5:140257168 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.827A>C (p.Asp276Ala) single nucleotide variant Inborn genetic diseases [RCV002822365] Chr5:140849322 [GRCh38]
Chr5:140228907 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.369G>C (p.Lys123Asn) single nucleotide variant Inborn genetic diseases [RCV002925110] Chr5:140856417 [GRCh38]
Chr5:140236002 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.949A>C (p.Lys317Gln) single nucleotide variant Inborn genetic diseases [RCV002821264] Chr5:140849444 [GRCh38]
Chr5:140229029 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.827C>A (p.Thr276Lys) single nucleotide variant Inborn genetic diseases [RCV002692321] Chr5:140927719 [GRCh38]
Chr5:140307304 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.2155A>G (p.Thr719Ala) single nucleotide variant Inborn genetic diseases [RCV002737874] Chr5:140884423 [GRCh38]
Chr5:140264008 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.167C>A (p.Ala56Glu) single nucleotide variant Inborn genetic diseases [RCV002925627] Chr5:140856215 [GRCh38]
Chr5:140235800 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.917C>T (p.Thr306Ile) single nucleotide variant Inborn genetic diseases [RCV002884434] Chr5:140870020 [GRCh38]
Chr5:140249605 [GRCh37]
Chr5:5q31.3
likely benign
NM_018902.5(PCDHA11):c.158G>A (p.Gly53Glu) single nucleotide variant Inborn genetic diseases [RCV002739296] Chr5:140869261 [GRCh38]
Chr5:140248846 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1682A>T (p.Asn561Ile) single nucleotide variant Inborn genetic diseases [RCV002661857] Chr5:140883950 [GRCh38]
Chr5:140263535 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.680G>C (p.Arg227Pro) single nucleotide variant Inborn genetic diseases [RCV002951436] Chr5:140869783 [GRCh38]
Chr5:140249368 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.778C>A (p.Pro260Thr) single nucleotide variant Inborn genetic diseases [RCV002848739] Chr5:140927670 [GRCh38]
Chr5:140307255 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.394G>A (p.Val132Met) single nucleotide variant Inborn genetic diseases [RCV002845994] Chr5:140869497 [GRCh38]
Chr5:140249082 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1310C>G (p.Thr437Arg) single nucleotide variant Inborn genetic diseases [RCV002660555] Chr5:140870413 [GRCh38]
Chr5:140249998 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1765G>T (p.Val589Leu) single nucleotide variant Inborn genetic diseases [RCV002926371] Chr5:140850260 [GRCh38]
Chr5:140229845 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.14G>T (p.Trp5Leu) single nucleotide variant Inborn genetic diseases [RCV002738824] Chr5:140882282 [GRCh38]
Chr5:140261867 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1490G>T (p.Arg497Leu) single nucleotide variant Inborn genetic diseases [RCV002977684] Chr5:140876962 [GRCh38]
Chr5:140256547 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.4C>G (p.Leu2Val) single nucleotide variant Inborn genetic diseases [RCV002869499] Chr5:140882272 [GRCh38]
Chr5:140261857 [GRCh37]
Chr5:5q31.3
likely benign
NM_018898.5(PCDHAC1):c.540C>G (p.Ser180Arg) single nucleotide variant Inborn genetic diseases [RCV002738883] Chr5:140927432 [GRCh38]
Chr5:140307017 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.489G>T (p.Glu163Asp) single nucleotide variant Inborn genetic diseases [RCV002926068] Chr5:140856537 [GRCh38]
Chr5:140236122 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.418G>A (p.Val140Ile) single nucleotide variant Inborn genetic diseases [RCV002758403] Chr5:140875890 [GRCh38]
Chr5:140255475 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.2011G>C (p.Gly671Arg) single nucleotide variant Inborn genetic diseases [RCV002757352] Chr5:140858059 [GRCh38]
Chr5:140237644 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.1193G>A (p.Arg398Gln) single nucleotide variant Inborn genetic diseases [RCV002737088] Chr5:140967959 [GRCh38]
Chr5:140347544 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1741C>T (p.Pro581Ser) single nucleotide variant Inborn genetic diseases [RCV002799022] Chr5:140870844 [GRCh38]
Chr5:140250429 [GRCh37]
Chr5:5q31.3
likely benign
NM_031857.2(PCDHA9):c.1846G>T (p.Ala616Ser) single nucleotide variant Inborn genetic diseases [RCV002703902] Chr5:140850341 [GRCh38]
Chr5:140229926 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.2084A>G (p.Asp695Gly) single nucleotide variant Inborn genetic diseases [RCV002888277] Chr5:140850579 [GRCh38]
Chr5:140230164 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1897A>C (p.Thr633Pro) single nucleotide variant Inborn genetic diseases [RCV002784558] Chr5:140877369 [GRCh38]
Chr5:140256954 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.913G>C (p.Asp305His) single nucleotide variant Inborn genetic diseases [RCV002694633] Chr5:140856961 [GRCh38]
Chr5:140236546 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.452A>G (p.Asp151Gly) single nucleotide variant Inborn genetic diseases [RCV002977034] Chr5:140927344 [GRCh38]
Chr5:140306929 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1555G>T (p.Ala519Ser) single nucleotide variant Inborn genetic diseases [RCV002951594] Chr5:140877027 [GRCh38]
Chr5:140256612 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.2212G>T (p.Gly738Cys) single nucleotide variant Inborn genetic diseases [RCV002925632] Chr5:140968978 [GRCh38]
Chr5:140348563 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.1292G>A (p.Arg431Gln) single nucleotide variant Inborn genetic diseases [RCV002694026] Chr5:140968058 [GRCh38]
Chr5:140347643 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1795G>A (p.Ala599Thr) single nucleotide variant Inborn genetic diseases [RCV002708804] Chr5:140877267 [GRCh38]
Chr5:140256852 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1952T>G (p.Val651Gly) single nucleotide variant Inborn genetic diseases [RCV002786920] Chr5:140884220 [GRCh38]
Chr5:140263805 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.1195A>C (p.Lys399Gln) single nucleotide variant Inborn genetic diseases [RCV002830954] Chr5:140967961 [GRCh38]
Chr5:140347546 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1511T>A (p.Leu504Gln) single nucleotide variant Inborn genetic diseases [RCV002712651] Chr5:140850006 [GRCh38]
Chr5:140229591 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.934A>G (p.Asn312Asp) single nucleotide variant Inborn genetic diseases [RCV002768440] Chr5:140870037 [GRCh38]
Chr5:140249622 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1213T>C (p.Ser405Pro) single nucleotide variant Inborn genetic diseases [RCV002985824] Chr5:140857261 [GRCh38]
Chr5:140236846 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1688C>T (p.Pro563Leu) single nucleotide variant Inborn genetic diseases [RCV002697965] Chr5:140877160 [GRCh38]
Chr5:140256745 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2098A>G (p.Ile700Val) single nucleotide variant Inborn genetic diseases [RCV002987483] Chr5:140871201 [GRCh38]
Chr5:140250786 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1477T>C (p.Ser493Pro) single nucleotide variant Inborn genetic diseases [RCV002854352] Chr5:140849972 [GRCh38]
Chr5:140229557 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.269T>C (p.Ile90Thr) single nucleotide variant Inborn genetic diseases [RCV002892834] Chr5:140875741 [GRCh38]
Chr5:140255326 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.535G>A (p.Gly179Ser) single nucleotide variant Inborn genetic diseases [RCV002763242] Chr5:140927427 [GRCh38]
Chr5:140307012 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1888G>C (p.Glu630Gln) single nucleotide variant Inborn genetic diseases [RCV002787141] Chr5:140884156 [GRCh38]
Chr5:140263741 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1342G>A (p.Val448Met) single nucleotide variant Inborn genetic diseases [RCV002664885] Chr5:140849837 [GRCh38]
Chr5:140229422 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.920A>C (p.Glu307Ala) single nucleotide variant Inborn genetic diseases [RCV003004107] Chr5:140876392 [GRCh38]
Chr5:140255977 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.2043C>G (p.Asn681Lys) single nucleotide variant Inborn genetic diseases [RCV002874674] Chr5:140928935 [GRCh38]
Chr5:140308520 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1529A>G (p.His510Arg) single nucleotide variant Inborn genetic diseases [RCV002955115] Chr5:140857577 [GRCh38]
Chr5:140237162 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.712A>T (p.Asn238Tyr) single nucleotide variant Inborn genetic diseases [RCV002664656] Chr5:140882980 [GRCh38]
Chr5:140262565 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.757G>A (p.Glu253Lys) single nucleotide variant Inborn genetic diseases [RCV002916491] Chr5:140883025 [GRCh38]
Chr5:140262610 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.2252G>A (p.Arg751Lys) single nucleotide variant Inborn genetic diseases [RCV002984541] Chr5:140969018 [GRCh38]
Chr5:140348603 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.2164C>T (p.Arg722Trp) single nucleotide variant Inborn genetic diseases [RCV002764974] Chr5:140850659 [GRCh38]
Chr5:140230244 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.185G>T (p.Arg62Leu) single nucleotide variant Inborn genetic diseases [RCV002931813] Chr5:140848680 [GRCh38]
Chr5:140228265 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1222A>C (p.Ile408Leu) single nucleotide variant Inborn genetic diseases [RCV002699601] Chr5:140928114 [GRCh38]
Chr5:140307699 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1370A>G (p.Gln457Arg) single nucleotide variant Inborn genetic diseases [RCV002709547] Chr5:140849865 [GRCh38]
Chr5:140229450 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1517C>T (p.Ala506Val) single nucleotide variant Inborn genetic diseases [RCV002712475] Chr5:140928409 [GRCh38]
Chr5:140307994 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.452G>T (p.Arg151Leu) single nucleotide variant Inborn genetic diseases [RCV002697259] Chr5:140848947 [GRCh38]
Chr5:140228532 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1964A>T (p.Glu655Val) single nucleotide variant Inborn genetic diseases [RCV002696883] Chr5:140858012 [GRCh38]
Chr5:140237597 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1217C>T (p.Ser406Leu) single nucleotide variant Inborn genetic diseases [RCV002826050] Chr5:140849712 [GRCh38]
Chr5:140229297 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1544G>T (p.Gly515Val) single nucleotide variant Inborn genetic diseases [RCV002698293] Chr5:140877016 [GRCh38]
Chr5:140256601 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1895C>G (p.Thr632Arg) single nucleotide variant Inborn genetic diseases [RCV002699380] Chr5:140870998 [GRCh38]
Chr5:140250583 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2050G>C (p.Gly684Arg) single nucleotide variant Inborn genetic diseases [RCV002985952] Chr5:140871153 [GRCh38]
Chr5:140250738 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.119A>T (p.His40Leu) single nucleotide variant Inborn genetic diseases [RCV003003806] Chr5:140856167 [GRCh38]
Chr5:140235752 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.790C>G (p.Pro264Ala) single nucleotide variant Inborn genetic diseases [RCV002850206] Chr5:140849285 [GRCh38]
Chr5:140228870 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1447G>T (p.Ala483Ser) single nucleotide variant Inborn genetic diseases [RCV003004861] Chr5:140870550 [GRCh38]
Chr5:140250135 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1895G>C (p.Ser632Thr) single nucleotide variant Inborn genetic diseases [RCV002985049] Chr5:140877367 [GRCh38]
Chr5:140256952 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2269G>A (p.Val757Met) single nucleotide variant Inborn genetic diseases [RCV002804633] Chr5:140871372 [GRCh38]
Chr5:140250957 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.492C>G (p.Ser164Arg) single nucleotide variant Inborn genetic diseases [RCV002644598] Chr5:140927384 [GRCh38]
Chr5:140306969 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1129C>A (p.Arg377Ser) single nucleotide variant Inborn genetic diseases [RCV002983774] Chr5:140876601 [GRCh38]
Chr5:140256186 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1928G>A (p.Arg643His) single nucleotide variant Inborn genetic diseases [RCV002787411] Chr5:140871031 [GRCh38]
Chr5:140250616 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.551A>G (p.Lys184Arg) single nucleotide variant Inborn genetic diseases [RCV002939204] Chr5:140856599 [GRCh38]
Chr5:140236184 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.805C>G (p.Pro269Ala) single nucleotide variant Inborn genetic diseases [RCV002718396] Chr5:140876277 [GRCh38]
Chr5:140255862 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.1589G>C (p.Ser530Thr) single nucleotide variant Inborn genetic diseases [RCV002940783] Chr5:140968355 [GRCh38]
Chr5:140347940 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1166C>T (p.Thr389Met) single nucleotide variant Inborn genetic diseases [RCV002808523] Chr5:140870269 [GRCh38]
Chr5:140249854 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1396G>A (p.Glu466Lys) single nucleotide variant Inborn genetic diseases [RCV002941679] Chr5:140883664 [GRCh38]
Chr5:140263249 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.762C>G (p.Asn254Lys) single nucleotide variant Inborn genetic diseases [RCV002717945] Chr5:140883030 [GRCh38]
Chr5:140262615 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1649A>G (p.Asp550Gly) single nucleotide variant Inborn genetic diseases [RCV002896573] Chr5:140928541 [GRCh38]
Chr5:140308126 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.2192C>G (p.Ala731Gly) single nucleotide variant Inborn genetic diseases [RCV002808734] Chr5:140884460 [GRCh38]
Chr5:140264045 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.973A>G (p.Lys325Glu) single nucleotide variant Inborn genetic diseases [RCV002670640] Chr5:140927865 [GRCh38]
Chr5:140307450 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2295G>T (p.Lys765Asn) single nucleotide variant Inborn genetic diseases [RCV002897363] Chr5:140871398 [GRCh38]
Chr5:140250983 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.187G>C (p.Glu63Gln) single nucleotide variant Inborn genetic diseases [RCV002714276] Chr5:140927079 [GRCh38]
Chr5:140306664 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1292G>A (p.Gly431Asp) single nucleotide variant Inborn genetic diseases [RCV002832403] Chr5:140883560 [GRCh38]
Chr5:140263145 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.2236A>G (p.Thr746Ala) single nucleotide variant Inborn genetic diseases [RCV002672346] Chr5:140929128 [GRCh38]
Chr5:140308713 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1319G>C (p.Arg440Thr) single nucleotide variant Inborn genetic diseases [RCV002769105] Chr5:140876791 [GRCh38]
Chr5:140256376 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1501C>A (p.Arg501Ser) single nucleotide variant Inborn genetic diseases [RCV002807367] Chr5:140870604 [GRCh38]
Chr5:140250189 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.821A>G (p.Asn274Ser) single nucleotide variant Inborn genetic diseases [RCV002807709] Chr5:140876293 [GRCh38]
Chr5:140255878 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1865G>A (p.Arg622His) single nucleotide variant Inborn genetic diseases [RCV002648683] Chr5:140870968 [GRCh38]
Chr5:140250553 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1248G>C (p.Glu416Asp) single nucleotide variant Inborn genetic diseases [RCV002896459] Chr5:140849743 [GRCh38]
Chr5:140229328 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.406G>A (p.Val136Met) single nucleotide variant Inborn genetic diseases [RCV002832459] Chr5:140967172 [GRCh38]
Chr5:140346757 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.2242T>G (p.Trp748Gly) single nucleotide variant Inborn genetic diseases [RCV002719317] Chr5:140877714 [GRCh38]
Chr5:140257299 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.460C>A (p.Leu154Ile) single nucleotide variant Inborn genetic diseases [RCV002807841] Chr5:140875932 [GRCh38]
Chr5:140255517 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1000T>C (p.Cys334Arg) single nucleotide variant Inborn genetic diseases [RCV002939472] Chr5:140883268 [GRCh38]
Chr5:140262853 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.497C>T (p.Ala166Val) single nucleotide variant Inborn genetic diseases [RCV002746941] Chr5:140848992 [GRCh38]
Chr5:140228577 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1565C>T (p.Pro522Leu) single nucleotide variant Inborn genetic diseases [RCV002808059] Chr5:140877037 [GRCh38]
Chr5:140256622 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1406C>A (p.Pro469Gln) single nucleotide variant Inborn genetic diseases [RCV002673022] Chr5:140883674 [GRCh38]
Chr5:140263259 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1705G>A (p.Ala569Thr) single nucleotide variant Inborn genetic diseases [RCV002987839] Chr5:140870808 [GRCh38]
Chr5:140250393 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.2221A>T (p.Ser741Cys) single nucleotide variant Inborn genetic diseases [RCV002719671] Chr5:140858269 [GRCh38]
Chr5:140237854 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.2093T>C (p.Val698Ala) single nucleotide variant Inborn genetic diseases [RCV002832401] Chr5:140877565 [GRCh38]
Chr5:140257150 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1522G>A (p.Val508Met) single nucleotide variant Inborn genetic diseases [RCV002921678] Chr5:140876994 [GRCh38]
Chr5:140256579 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1748T>C (p.Val583Ala) single nucleotide variant Inborn genetic diseases [RCV002813122] Chr5:140928640 [GRCh38]
Chr5:140308225 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.913T>C (p.Tyr305His) single nucleotide variant Inborn genetic diseases [RCV002940866] Chr5:140876385 [GRCh38]
Chr5:140255970 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1230C>A (p.Asp410Glu) single nucleotide variant Inborn genetic diseases [RCV002747243] Chr5:140876702 [GRCh38]
Chr5:140256287 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.941A>G (p.Asp314Gly) single nucleotide variant Inborn genetic diseases [RCV002747808] Chr5:140927833 [GRCh38]
Chr5:140307418 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.1067T>G (p.Val356Gly) single nucleotide variant Inborn genetic diseases [RCV002940412] Chr5:140967833 [GRCh38]
Chr5:140347418 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.485G>T (p.Gly162Val) single nucleotide variant Inborn genetic diseases [RCV002724122] Chr5:140856533 [GRCh38]
Chr5:140236118 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.700G>A (p.Asp234Asn) single nucleotide variant Inborn genetic diseases [RCV002677139] Chr5:140849195 [GRCh38]
Chr5:140228780 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1715G>A (p.Gly572Asp) single nucleotide variant Inborn genetic diseases [RCV002680038] Chr5:140850210 [GRCh38]
Chr5:140229795 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1637G>A (p.Gly546Asp) single nucleotide variant Inborn genetic diseases [RCV002944737] Chr5:140877109 [GRCh38]
Chr5:140256694 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1165G>T (p.Ala389Ser) single nucleotide variant Inborn genetic diseases [RCV002944880] Chr5:140928057 [GRCh38]
Chr5:140307642 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1608C>A (p.Ser536Arg) single nucleotide variant Inborn genetic diseases [RCV002652548] Chr5:140850103 [GRCh38]
Chr5:140229688 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1921G>A (p.Asp641Asn) single nucleotide variant Inborn genetic diseases [RCV002657470] Chr5:140850416 [GRCh38]
Chr5:140230001 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1250G>A (p.Ser417Asn) single nucleotide variant Inborn genetic diseases [RCV002680247] Chr5:140876722 [GRCh38]
Chr5:140256307 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1438C>T (p.Arg480Trp) single nucleotide variant Inborn genetic diseases [RCV002677367] Chr5:140849933 [GRCh38]
Chr5:140229518 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.1349C>T (p.Thr450Ile) single nucleotide variant Inborn genetic diseases [RCV002679517] Chr5:140968115 [GRCh38]
Chr5:140347700 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1449C>A (p.Asp483Glu) single nucleotide variant Inborn genetic diseases [RCV002723355] Chr5:140849944 [GRCh38]
Chr5:140229529 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.358A>G (p.Asn120Asp) single nucleotide variant Inborn genetic diseases [RCV003296310] Chr5:140869461 [GRCh38]
Chr5:140249046 [GRCh37]
Chr5:5q31.3
likely benign
NM_031857.2(PCDHA9):c.445G>A (p.Asp149Asn) single nucleotide variant Inborn genetic diseases [RCV003299258] Chr5:140848940 [GRCh38]
Chr5:140228525 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1500C>G (p.Asp500Glu) single nucleotide variant Inborn genetic diseases [RCV003255722] Chr5:140870603 [GRCh38]
Chr5:140250188 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.196G>A (p.Val66Met) single nucleotide variant Inborn genetic diseases [RCV003255727] Chr5:140875668 [GRCh38]
Chr5:140255253 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1546A>C (p.Lys516Gln) single nucleotide variant Inborn genetic diseases [RCV003255731] Chr5:140883814 [GRCh38]
Chr5:140263399 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1508C>T (p.Ser503Leu) single nucleotide variant Inborn genetic diseases [RCV003189871] Chr5:140850003 [GRCh38]
Chr5:140229588 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2276C>T (p.Ser759Phe) single nucleotide variant Inborn genetic diseases [RCV003195597] Chr5:140871379 [GRCh38]
Chr5:140250964 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.2090A>G (p.Asn697Ser) single nucleotide variant Inborn genetic diseases [RCV003197913] Chr5:140884358 [GRCh38]
Chr5:140263943 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1231G>T (p.Ala411Ser) single nucleotide variant Inborn genetic diseases [RCV003192734] Chr5:140857279 [GRCh38]
Chr5:140236864 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1999T>A (p.Phe667Ile) single nucleotide variant Inborn genetic diseases [RCV003220292] Chr5:140928891 [GRCh38]
Chr5:140308476 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.2090A>T (p.Tyr697Phe) single nucleotide variant Inborn genetic diseases [RCV003190906] Chr5:140858138 [GRCh38]
Chr5:140237723 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.263C>G (p.Ser88Cys) single nucleotide variant Inborn genetic diseases [RCV003173238] Chr5:140875735 [GRCh38]
Chr5:140255320 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1372T>C (p.Ser458Pro) single nucleotide variant Inborn genetic diseases [RCV003185543] Chr5:140849867 [GRCh38]
Chr5:140229452 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.1853C>T (p.Ala618Val) single nucleotide variant Inborn genetic diseases [RCV003214217] Chr5:140877325 [GRCh38]
Chr5:140256910 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.776A>G (p.Gln259Arg) single nucleotide variant Inborn genetic diseases [RCV003211443] Chr5:140967542 [GRCh38]
Chr5:140347127 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.510A>T (p.Lys170Asn) single nucleotide variant Inborn genetic diseases [RCV003206100] Chr5:140856558 [GRCh38]
Chr5:140236143 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1885G>A (p.Glu629Lys) single nucleotide variant Inborn genetic diseases [RCV003210304] Chr5:140870988 [GRCh38]
Chr5:140250573 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2165G>T (p.Trp722Leu) single nucleotide variant Inborn genetic diseases [RCV003174299] Chr5:140871268 [GRCh38]
Chr5:140250853 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.517A>G (p.Met173Val) single nucleotide variant Inborn genetic diseases [RCV003212950] Chr5:140927409 [GRCh38]
Chr5:140306994 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1337C>G (p.Ala446Gly) single nucleotide variant Inborn genetic diseases [RCV003209566] Chr5:140849832 [GRCh38]
Chr5:140229417 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.278A>T (p.Glu93Val) single nucleotide variant Inborn genetic diseases [RCV003196536] Chr5:140848773 [GRCh38]
Chr5:140228358 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.2018C>G (p.Pro673Arg) single nucleotide variant Inborn genetic diseases [RCV003200951] Chr5:140928910 [GRCh38]
Chr5:140308495 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.272G>T (p.Arg91Leu) single nucleotide variant Inborn genetic diseases [RCV003198796] Chr5:140856320 [GRCh38]
Chr5:140235905 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.668C>T (p.Thr223Ile) single nucleotide variant Inborn genetic diseases [RCV003206101] Chr5:140849163 [GRCh38]
Chr5:140228748 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.533T>G (p.Phe178Cys) single nucleotide variant Inborn genetic diseases [RCV003199407] Chr5:140849028 [GRCh38]
Chr5:140228613 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1114A>G (p.Ser372Gly) single nucleotide variant Inborn genetic diseases [RCV003214244] Chr5:140870217 [GRCh38]
Chr5:140249802 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.143C>T (p.Ala48Val) single nucleotide variant Inborn genetic diseases [RCV003282780] Chr5:140856191 [GRCh38]
Chr5:140235776 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1277C>G (p.Thr426Ser) single nucleotide variant Inborn genetic diseases [RCV003302403] Chr5:140883545 [GRCh38]
Chr5:140263130 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1318A>C (p.Ser440Arg) single nucleotide variant Inborn genetic diseases [RCV003302404] Chr5:140883586 [GRCh38]
Chr5:140263171 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1361C>T (p.Ala454Val) single nucleotide variant Inborn genetic diseases [RCV003302405] Chr5:140883629 [GRCh38]
Chr5:140263214 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1440G>C (p.Gln480His) single nucleotide variant Inborn genetic diseases [RCV003302407] Chr5:140883708 [GRCh38]
Chr5:140263293 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1674C>G (p.Asn558Lys) single nucleotide variant Inborn genetic diseases [RCV003178009] Chr5:140857722 [GRCh38]
Chr5:140237307 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.151G>A (p.Asp51Asn) single nucleotide variant Inborn genetic diseases [RCV003210264] Chr5:140882419 [GRCh38]
Chr5:140262004 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.2306C>A (p.Ala769Asp) single nucleotide variant Inborn genetic diseases [RCV003197571] Chr5:140858354 [GRCh38]
Chr5:140237939 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.221T>C (p.Leu74Pro) single nucleotide variant Inborn genetic diseases [RCV003173233] Chr5:140856269 [GRCh38]
Chr5:140235854 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1123G>C (p.Val375Leu) single nucleotide variant Inborn genetic diseases [RCV003205958] Chr5:140928015 [GRCh38]
Chr5:140307600 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1288G>A (p.Gly430Ser) single nucleotide variant Inborn genetic diseases [RCV003215237] Chr5:140870391 [GRCh38]
Chr5:140249976 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1984G>A (p.Ala662Thr) single nucleotide variant Inborn genetic diseases [RCV003220690] Chr5:140858032 [GRCh38]
Chr5:140237617 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1750T>C (p.Ser584Pro) single nucleotide variant Inborn genetic diseases [RCV003184022] Chr5:140877222 [GRCh38]
Chr5:140256807 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1844G>A (p.Gly615Asp) single nucleotide variant Inborn genetic diseases [RCV003215818] Chr5:140870947 [GRCh38]
Chr5:140250532 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2233G>A (p.Gly745Arg) single nucleotide variant Inborn genetic diseases [RCV003203954] Chr5:140871336 [GRCh38]
Chr5:140250921 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1189C>A (p.Leu397Met) single nucleotide variant Inborn genetic diseases [RCV003217344] Chr5:140883457 [GRCh38]
Chr5:140263042 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1190T>G (p.Leu397Arg) single nucleotide variant Inborn genetic diseases [RCV003217345] Chr5:140883458 [GRCh38]
Chr5:140263043 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1405C>G (p.Pro469Ala) single nucleotide variant Inborn genetic diseases [RCV003302406] Chr5:140883673 [GRCh38]
Chr5:140263258 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1628C>G (p.Pro543Arg) single nucleotide variant Inborn genetic diseases [RCV003306505] Chr5:140850123 [GRCh38]
Chr5:140229708 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1813T>A (p.Trp605Arg) single nucleotide variant Inborn genetic diseases [RCV003357481] Chr5:140857861 [GRCh38]
Chr5:140237446 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1915C>T (p.Arg639Trp) single nucleotide variant Inborn genetic diseases [RCV003359670] Chr5:140928807 [GRCh38]
Chr5:140308392 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.31G>T (p.Gly11Cys) single nucleotide variant Inborn genetic diseases [RCV003359629] Chr5:140848526 [GRCh38]
Chr5:140228111 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1726G>A (p.Ala576Thr) single nucleotide variant Inborn genetic diseases [RCV003359040] Chr5:140877198 [GRCh38]
Chr5:140256783 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1067G>A (p.Gly356Asp) single nucleotide variant Inborn genetic diseases [RCV003343417] Chr5:140927959 [GRCh38]
Chr5:140307544 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1993C>T (p.Leu665Phe) single nucleotide variant Inborn genetic diseases [RCV003359955] Chr5:140858041 [GRCh38]
Chr5:140237626 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.604G>A (p.Val202Met) single nucleotide variant Inborn genetic diseases [RCV003371568] Chr5:140927496 [GRCh38]
Chr5:140307081 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.286T>G (p.Cys96Gly) single nucleotide variant Inborn genetic diseases [RCV003376152] Chr5:140882554 [GRCh38]
Chr5:140262139 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.856G>A (p.Val286Met) single nucleotide variant Inborn genetic diseases [RCV003347967] Chr5:140927748 [GRCh38]
Chr5:140307333 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.848T>C (p.Leu283Ser) single nucleotide variant Inborn genetic diseases [RCV003383422] Chr5:140856896 [GRCh38]
Chr5:140236481 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.140G>C (p.Arg47Pro) single nucleotide variant Inborn genetic diseases [RCV003366972] Chr5:140882408 [GRCh38]
Chr5:140261993 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.1582A>G (p.Ser528Gly) single nucleotide variant Inborn genetic diseases [RCV003348290] Chr5:140968348 [GRCh38]
Chr5:140347933 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.1214C>G (p.Ser405Trp) single nucleotide variant Inborn genetic diseases [RCV003351034] Chr5:140870317 [GRCh38]
Chr5:140249902 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.719C>T (p.Pro240Leu) single nucleotide variant Inborn genetic diseases [RCV003355131] Chr5:140882987 [GRCh38]
Chr5:140262572 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1195A>T (p.Ile399Phe) single nucleotide variant Inborn genetic diseases [RCV003369708] Chr5:140928087 [GRCh38]
Chr5:140307672 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1289G>A (p.Gly430Glu) single nucleotide variant Inborn genetic diseases [RCV003348430] Chr5:140849784 [GRCh38]
Chr5:140229369 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1664T>G (p.Val555Gly) single nucleotide variant Inborn genetic diseases [RCV003373969] Chr5:140877136 [GRCh38]
Chr5:140256721 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.2162G>T (p.Cys721Phe) single nucleotide variant Inborn genetic diseases [RCV003364932] Chr5:140858210 [GRCh38]
Chr5:140237795 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.1070C>T (p.Pro357Leu) single nucleotide variant Inborn genetic diseases [RCV003384046] Chr5:140857118 [GRCh38]
Chr5:140236703 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.1193T>C (p.Val398Ala) single nucleotide variant Inborn genetic diseases [RCV003370887] Chr5:140876665 [GRCh38]
Chr5:140256250 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1444G>A (p.Ala482Thr) single nucleotide variant Inborn genetic diseases [RCV003353855] Chr5:140883712 [GRCh38]
Chr5:140263297 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.849G>T (p.Arg283Ser) single nucleotide variant Inborn genetic diseases [RCV003372425] Chr5:140883117 [GRCh38]
Chr5:140262702 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.211G>T (p.Gly71Trp) single nucleotide variant Inborn genetic diseases [RCV003349756] Chr5:140856259 [GRCh38]
Chr5:140235844 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.2134G>T (p.Val712Leu) single nucleotide variant Inborn genetic diseases [RCV003373137] Chr5:140884402 [GRCh38]
Chr5:140263987 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.2306T>C (p.Met769Thr) single nucleotide variant Inborn genetic diseases [RCV003364777] Chr5:140871409 [GRCh38]
Chr5:140250994 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1010T>C (p.Leu337Ser) single nucleotide variant Inborn genetic diseases [RCV003364396] Chr5:140883278 [GRCh38]
Chr5:140262863 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.989T>C (p.Val330Ala) single nucleotide variant Inborn genetic diseases [RCV003347858] Chr5:140927881 [GRCh38]
Chr5:140307466 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.995A>G (p.His332Arg) single nucleotide variant Inborn genetic diseases [RCV003374500] Chr5:140870098 [GRCh38]
Chr5:140249683 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.182C>A (p.Pro61Gln) single nucleotide variant Inborn genetic diseases [RCV003383515] Chr5:140882450 [GRCh38]
Chr5:140262035 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.2141C>G (p.Thr714Arg) single nucleotide variant Inborn genetic diseases [RCV003383516] Chr5:140884409 [GRCh38]
Chr5:140263994 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018903.4(PCDHA12):c.145G>T (p.Ala49Ser) single nucleotide variant Inborn genetic diseases [RCV003375071] Chr5:140875617 [GRCh38]
Chr5:140255202 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.154G>A (p.Gly52Arg) single nucleotide variant Inborn genetic diseases [RCV003363382] Chr5:140856202 [GRCh38]
Chr5:140235787 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018902.5(PCDHA11):c.653G>A (p.Gly218Glu) single nucleotide variant Inborn genetic diseases [RCV003366200] Chr5:140869756 [GRCh38]
Chr5:140249341 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1735T>G (p.Leu579Val) single nucleotide variant Inborn genetic diseases [RCV003369325] Chr5:140928627 [GRCh38]
Chr5:140308212 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018898.5(PCDHAC1):c.1771G>T (p.Gly591Cys) single nucleotide variant Inborn genetic diseases [RCV003386675] Chr5:140928663 [GRCh38]
Chr5:140308248 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.850C>G (p.Pro284Ala) single nucleotide variant Inborn genetic diseases [RCV003369648] Chr5:140883118 [GRCh38]
Chr5:140262703 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018904.3(PCDHA13):c.1955A>G (p.Lys652Arg) single nucleotide variant Inborn genetic diseases [RCV003371965] Chr5:140884223 [GRCh38]
Chr5:140263808 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018900.4(PCDHA1):c.2394+59919G>C single nucleotide variant not provided [RCV003429793] Chr5:140848603 [GRCh38]
Chr5:140228188 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.2220T>C (p.Ser740=) single nucleotide variant not provided [RCV003429804] Chr5:140858268 [GRCh38]
Chr5:140237853 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.2247G>A (p.Ser749=) single nucleotide variant not provided [RCV003429805] Chr5:140858295 [GRCh38]
Chr5:140237880 [GRCh37]
Chr5:5q31.3
likely benign
NM_018907.4(PCDHA4):c.2385+53642A>G single nucleotide variant not provided [RCV003429807] Chr5:140863214 [GRCh38]
Chr5:140242799 [GRCh37]
Chr5:5q31.3
likely benign
NM_018907.4(PCDHA4):c.2385+59713A>C single nucleotide variant not provided [RCV003429809] Chr5:140869285 [GRCh38]
Chr5:140248870 [GRCh37]
Chr5:5q31.3
likely benign
NM_018902.5(PCDHA11):c.1407A>G (p.Pro469=) single nucleotide variant not provided [RCV003429811] Chr5:140870510 [GRCh38]
Chr5:140250095 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.1813G>T (p.Ala605Ser) single nucleotide variant not provided [RCV003429814] Chr5:140877285 [GRCh38]
Chr5:140256870 [GRCh37]
Chr5:5q31.3
likely benign
NM_018904.3(PCDHA13):c.1428G>C (p.Thr476=) single nucleotide variant not provided [RCV003429815] Chr5:140883696 [GRCh38]
Chr5:140263281 [GRCh37]
Chr5:5q31.3
likely benign
NM_018899.6(PCDHAC2):c.1161C>G (p.Leu387=) single nucleotide variant not provided [RCV003429820] Chr5:140967927 [GRCh38]
Chr5:140347512 [GRCh37]
Chr5:5q31.3
likely benign
NM_018899.6(PCDHAC2):c.2460G>A (p.Ser820=) single nucleotide variant not provided [RCV003429821] Chr5:140969226 [GRCh38]
Chr5:140348811 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.2052C>T (p.Gly684=) single nucleotide variant not provided [RCV003457447] Chr5:140858100 [GRCh38]
Chr5:140237685 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.1668C>T (p.Asp556=) single nucleotide variant not provided [RCV003428626] Chr5:140857716 [GRCh38]
Chr5:140237301 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.1416C>G (p.His472Gln) single nucleotide variant not provided [RCV003428625] Chr5:140857464 [GRCh38]
Chr5:140237049 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.1800T>C (p.Ser600=) single nucleotide variant not provided [RCV003429801] Chr5:140857848 [GRCh38]
Chr5:140237433 [GRCh37]
Chr5:5q31.3
likely benign
NM_018902.5(PCDHA11):c.516A>G (p.Leu172=) single nucleotide variant not provided [RCV003429810] Chr5:140869619 [GRCh38]
Chr5:140249204 [GRCh37]
Chr5:5q31.3
likely benign
NM_018904.3(PCDHA13):c.2164C>A (p.Arg722=) single nucleotide variant not provided [RCV003428629] Chr5:140884432 [GRCh38]
Chr5:140264017 [GRCh37]
Chr5:5q31.3
likely benign
NM_018907.4(PCDHA4):c.2385+53502A>G single nucleotide variant not provided [RCV003429806] Chr5:140863074 [GRCh38]
Chr5:140242659 [GRCh37]
Chr5:5q31.3
likely benign
NM_018902.5(PCDHA11):c.98A>G (p.Tyr33Cys) single nucleotide variant not provided [RCV003429808] Chr5:140869201 [GRCh38]
Chr5:140248786 [GRCh37]
Chr5:5q31.3
likely benign
NM_018907.4(PCDHA4):c.2385+74492C>A single nucleotide variant not provided [RCV003429817] Chr5:140884064 [GRCh38]
Chr5:140263649 [GRCh37]
Chr5:5q31.3
likely benign
NM_018898.5(PCDHAC1):c.1671T>C (p.Phe557=) single nucleotide variant not provided [RCV003429819] Chr5:140928563 [GRCh38]
Chr5:140308148 [GRCh37]
Chr5:5q31.3
likely benign
NM_018899.6(PCDHAC2):c.1911G>A (p.Leu637=) single nucleotide variant not provided [RCV003457448] Chr5:140968677 [GRCh38]
Chr5:140348262 [GRCh37]
Chr5:5q31.3
likely benign
NM_031857.2(PCDHA9):c.286T>G (p.Cys96Gly) single nucleotide variant not provided [RCV003429795] Chr5:140848781 [GRCh38]
Chr5:140228366 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.179A>C (p.Gln60Pro) single nucleotide variant not provided [RCV003429799] Chr5:140856227 [GRCh38]
Chr5:140235812 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.1863T>C (p.Phe621=) single nucleotide variant not provided [RCV003429802] Chr5:140857911 [GRCh38]
Chr5:140237496 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.2017C>T (p.Gln673Ter) single nucleotide variant not provided [RCV003429803] Chr5:140858065 [GRCh38]
Chr5:140237650 [GRCh37]
Chr5:5q31.3
likely benign
NM_018904.3(PCDHA13):c.2202G>A (p.Pro734=) single nucleotide variant not provided [RCV003429818] Chr5:140884470 [GRCh38]
Chr5:140264055 [GRCh37]
Chr5:5q31.3
likely benign
NM_031857.2(PCDHA9):c.2046G>T (p.Ala682=) single nucleotide variant not provided [RCV003428624] Chr5:140850541 [GRCh38]
Chr5:140230126 [GRCh37]
Chr5:5q31.3
likely benign
NM_031857.2(PCDHA9):c.123C>T (p.His41=) single nucleotide variant not provided [RCV003429794] Chr5:140848618 [GRCh38]
Chr5:140228203 [GRCh37]
Chr5:5q31.3
likely benign
NM_018907.4(PCDHA4):c.2385+39349C>A single nucleotide variant not provided [RCV003429796] Chr5:140848921 [GRCh38]
Chr5:140228506 [GRCh37]
Chr5:5q31.3
likely benign
NM_018907.4(PCDHA4):c.2385+39447A>G single nucleotide variant not provided [RCV003429797] Chr5:140849019 [GRCh38]
Chr5:140228604 [GRCh37]
Chr5:5q31.3
likely benign
NM_018903.4(PCDHA12):c.768A>G (p.Gln256=) single nucleotide variant not provided [RCV003429813] Chr5:140876240 [GRCh38]
Chr5:140255825 [GRCh37]
Chr5:5q31.3
likely benign
NM_018900.4(PCDHA1):c.2394+60504G>A single nucleotide variant not provided [RCV003429798] Chr5:140849188 [GRCh38]
Chr5:140228773 [GRCh37]
Chr5:5q31.3
likely benign
NM_018901.4(PCDHA10):c.1014_1022del (p.Glu338_Leu340del) deletion not provided [RCV003429800] Chr5:140857058..140857066 [GRCh38]
Chr5:140236643..140236651 [GRCh37]
Chr5:5q31.3
likely benign
NM_018902.5(PCDHA11):c.2391+12410G>A single nucleotide variant not provided [RCV003429816] Chr5:140883904 [GRCh38]
Chr5:140263489 [GRCh37]
Chr5:5q31.3
likely benign
NM_018900.4(PCDHA1):c.2394+59913C>G single nucleotide variant not provided [RCV003428623] Chr5:140848597 [GRCh38]
Chr5:140228182 [GRCh37]
Chr5:5q31.3
likely benign
NM_018902.5(PCDHA11):c.1800A>C (p.Ser600=) single nucleotide variant not provided [RCV003429812] Chr5:140870903 [GRCh38]
Chr5:140250488 [GRCh37]
Chr5:5q31.3
likely benign
NM_018907.4(PCDHA4):c.2385+53659C>T single nucleotide variant not provided [RCV003428627] Chr5:140863231 [GRCh38]
Chr5:140242816 [GRCh37]
Chr5:5q31.3
likely benign
NM_018904.3(PCDHA13):c.292C>A (p.Arg98=) single nucleotide variant not provided [RCV003428628] Chr5:140882560 [GRCh38]
Chr5:140262145 [GRCh37]
Chr5:5q31.3
likely benign
NM_018899.6(PCDHAC2):c.480G>T (p.Ser160=) single nucleotide variant not provided [RCV003428630] Chr5:140967246 [GRCh38]
Chr5:140346831 [GRCh37]
Chr5:5q31.3
likely benign
NM_031857.2(PCDHA9):c.1205A>G (p.Lys402Arg) single nucleotide variant Inborn genetic diseases [RCV003381902] Chr5:140849700 [GRCh38]
Chr5:140229285 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1649C>T (p.Thr550Met) single nucleotide variant Inborn genetic diseases [RCV003356844] Chr5:140850144 [GRCh38]
Chr5:140229729 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018901.4(PCDHA10):c.2296G>A (p.Asp766Asn) single nucleotide variant Inborn genetic diseases [RCV003341086] Chr5:140858344 [GRCh38]
Chr5:140237929 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031857.2(PCDHA9):c.1734C>G (p.Ser578Arg) single nucleotide variant Inborn genetic diseases [RCV003341087] Chr5:140850229 [GRCh38]
Chr5:140229814 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.2197C>T (p.Arg733Cys) single nucleotide variant Inborn genetic diseases [RCV003344465] Chr5:140968963 [GRCh38]
Chr5:140348548 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018899.6(PCDHAC2):c.2207C>A (p.Ala736Glu) single nucleotide variant Inborn genetic diseases [RCV003381089] Chr5:140968973 [GRCh38]
Chr5:140348558 [GRCh37]
Chr5:5q31.3
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2580
Count of miRNA genes:1058
Interacting mature miRNAs:1326
Transcripts:ENST00000378122, ENST00000532602
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
D5S658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,372,916 - 140,373,189UniSTSGRCh37
Build 365140,353,100 - 140,353,373RGDNCBI36
Celera5136,449,700 - 136,449,973RGD
Cytogenetic Map5q31UniSTS
HuRef5135,517,629 - 135,517,894UniSTS
Marshfield Genetic Map5142.92RGD
Marshfield Genetic Map5142.92UniSTS
Genethon Genetic Map5142.6UniSTS
Whitehead-RH Map5441.7UniSTS
Whitehead-YAC Contig Map5 UniSTS
NCBI RH Map5889.1UniSTS
RH91795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,389,215 - 140,389,359UniSTSGRCh37
Build 365140,369,399 - 140,369,543RGDNCBI36
Celera5136,465,994 - 136,466,138RGD
Cytogenetic Map5q31UniSTS
HuRef5135,533,914 - 135,534,058UniSTS
GeneMap99-GB4 RH Map5530.5UniSTS
RH122893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,344,075 - 140,344,397UniSTSGRCh37
Build 365140,324,259 - 140,324,581RGDNCBI36
Celera5136,420,859 - 136,421,181RGD
Cytogenetic Map5q31UniSTS
HuRef5135,488,790 - 135,489,112UniSTS
TNG Radiation Hybrid Map565054.0UniSTS
RH118816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,365,779 - 140,366,073UniSTSGRCh37
Build 365140,345,963 - 140,346,257RGDNCBI36
Celera5136,442,563 - 136,442,857RGD
Cytogenetic Map5q31UniSTS
HuRef5135,510,494 - 135,510,788UniSTS
TNG Radiation Hybrid Map565069.0UniSTS
D5S546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,240,136 - 140,240,231UniSTSGRCh37
Build 365140,220,320 - 140,220,415RGDNCBI36
Celera5136,316,944 - 136,317,039RGD
Cytogenetic Map5q31UniSTS
HuRef5135,384,875 - 135,384,970UniSTS
D5S1683E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,390,021 - 140,390,212UniSTSGRCh37
Build 365140,370,205 - 140,370,396RGDNCBI36
Celera5136,466,800 - 136,466,991RGD
Cytogenetic Map5q31UniSTS
HuRef5135,534,720 - 135,534,911UniSTS
SHGC-150174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,372,907 - 140,373,191UniSTSGRCh37
Build 365140,353,091 - 140,353,375RGDNCBI36
Celera5136,449,691 - 136,449,975RGD
Cytogenetic Map5q31UniSTS
HuRef5135,517,620 - 135,517,896UniSTS
TNG Radiation Hybrid Map565089.0UniSTS
TNG Radiation Hybrid Map174062.0UniSTS
bac5366T  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,362,911 - 140,363,118UniSTSGRCh37
Build 365140,343,095 - 140,343,302RGDNCBI36
Celera5136,439,695 - 136,439,902RGD
Cytogenetic Map5q31UniSTS
HuRef5135,507,626 - 135,507,833UniSTS
bac5373T  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,363,259 - 140,363,393UniSTSGRCh37
Build 365140,343,443 - 140,343,577RGDNCBI36
Celera5136,440,043 - 136,440,177RGD
Cytogenetic Map5q31UniSTS
HuRef5135,507,974 - 135,508,108UniSTS
PMC311048P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,362,060 - 140,362,148UniSTSGRCh37
Build 365140,342,244 - 140,342,332RGDNCBI36
Celera5136,438,844 - 136,438,932RGD
HuRef5135,506,775 - 135,506,863UniSTS
PCDHA4_1031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,390,470 - 140,391,194UniSTSGRCh37
Build 365140,370,654 - 140,371,378RGDNCBI36
Celera5136,467,249 - 136,467,973RGD
HuRef5135,535,169 - 135,535,893UniSTS
A004B11  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,307,787 - 140,307,943UniSTSGRCh37
Build 365140,287,971 - 140,288,127RGDNCBI36
Celera5136,384,600 - 136,384,756RGD
Cytogenetic Map5q31UniSTS
HuRef5135,452,522 - 135,452,678UniSTS
GeneMap99-GB4 RH Map5531.62UniSTS
NCBI RH Map5889.1UniSTS
RH15971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,390,200 - 140,390,359UniSTSGRCh37
Build 365140,370,384 - 140,370,543RGDNCBI36
Celera5136,466,979 - 136,467,138RGD
Cytogenetic Map5q31UniSTS
HuRef5135,534,899 - 135,535,058UniSTS
GeneMap99-GB4 RH Map5531.42UniSTS
NCBI RH Map5889.1UniSTS
IB766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,391,639 - 140,391,867UniSTSGRCh37
Build 365140,371,823 - 140,372,051RGDNCBI36
Celera5136,468,418 - 136,468,646RGD
Cytogenetic Map5q31UniSTS
HuRef5135,536,338 - 135,536,566UniSTS
GeneMap99-GB4 RH Map5531.42UniSTS
Whitehead-RH Map5441.7UniSTS
NCBI RH Map5889.1UniSTS
WI-19540  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,391,613 - 140,391,874UniSTSGRCh37
Build 365140,371,797 - 140,372,058RGDNCBI36
Celera5136,468,392 - 136,468,653RGD
Cytogenetic Map5q31UniSTS
HuRef5135,536,312 - 135,536,573UniSTS
GeneMap99-GB4 RH Map5531.72UniSTS
Whitehead-RH Map5441.7UniSTS
NCBI RH Map5889.1UniSTS
RH65516  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,390,919 - 140,391,093UniSTSGRCh37
Build 365140,371,103 - 140,371,277RGDNCBI36
Celera5136,467,698 - 136,467,872RGD
Cytogenetic Map5q31UniSTS
HuRef5135,535,618 - 135,535,792UniSTS
GeneMap99-GB4 RH Map5527.13UniSTS
NCBI RH Map5889.1UniSTS
PCDHA9_3148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,232,949 - 140,233,427UniSTSGRCh37
Build 365140,213,133 - 140,213,611RGDNCBI36
Celera5136,309,754 - 136,310,232RGD
HuRef5135,377,685 - 135,378,163UniSTS
PCDHAC1__5835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,308,699 - 140,309,481UniSTSGRCh37
Build 365140,288,883 - 140,289,665RGDNCBI36
Celera5136,385,512 - 136,386,294RGD
HuRef5135,453,434 - 135,454,216UniSTS
D8S2278  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p25.3-p24.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic MapXp22.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map12q14.3-q15UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q31UniSTS
D10S16   No map positions available.
L18441  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5q31UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map10q11.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16q24UniSTS
D1S1423  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p22.3-p21.32UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map9q12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map10p14-p13UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map11q23-q24UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map22cen-q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map4q28UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map1q41-q42UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map11q24.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3q13UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map9p21.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq27.2UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map20q11.21-q11.23UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map15q26UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p15.1-p14UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map7q32.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21-q24UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map8q24.12UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map6q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map20pter-p12UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map14q22.2UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p22-p21UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map10q22.3-q23.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map3p12.3UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map3q11.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6p24.2UniSTS
Cytogenetic Map20q13.33UniSTS
D11S2921  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map10q24.33UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic MapXp11.4-p11.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map18pter-p11.3UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map7q21.12UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11p13-p12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map5q12-q13UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic MapXq25-q26.3UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map12p11.22UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map9p11UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map15q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q22-qterUniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19p13.2-cenUniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map9q33UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic MapXq26.2UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map5p13.1-p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map6q14.3-q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map6q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map6q11.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map14q11.2-q21UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map5p14.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map9p13.1UniSTS
Cytogenetic Map9q34.13UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 1
Low 2 3 2 4 2 43 13 353 4 363 34 1
Below cutoff 1765 1447 1184 233 611 98 2801 1166 3156 212 796 1325 138 896 1754 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_000016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NG_050675 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NG_050677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_031857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB002343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC008468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC010223 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF152317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF152487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ007610 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK314303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC104802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC104804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000378122   ⟹   ENSP00000367362
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,847,772 - 140,854,671 (+)Ensembl
RefSeq Acc Id: ENST00000532602   ⟹   ENSP00000436042
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5140,848,382 - 141,012,347 (+)Ensembl
RefSeq Acc Id: NM_014005   ⟹   NP_054724
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,847,772 - 140,854,159 (+)NCBI
GRCh375140,227,357 - 140,391,929 (+)RGD
Build 365140,207,541 - 140,213,928 (+)NCBI Archive
Celera5136,304,162 - 136,468,708 (+)RGD
HuRef5135,372,092 - 135,536,628 (+)ENTREZGENE
CHM1_15139,660,543 - 139,666,930 (+)NCBI
T2T-CHM13v2.05141,373,097 - 141,379,484 (+)NCBI
Sequence:
RefSeq Acc Id: NM_031857   ⟹   NP_114063
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,848,382 - 141,012,347 (+)NCBI
GRCh375140,227,357 - 140,391,929 (+)RGD
Build 365140,207,541 - 140,372,113 (+)NCBI Archive
Celera5136,304,162 - 136,468,708 (+)RGD
HuRef5135,372,092 - 135,536,628 (+)ENTREZGENE
CHM1_15139,660,543 - 139,825,092 (+)NCBI
T2T-CHM13v2.05141,373,707 - 141,537,634 (+)NCBI
Sequence:
RefSeq Acc Id: NP_114063   ⟸   NM_031857
- Peptide Label: isoform 1 precursor
- UniProtKB: O15053 (UniProtKB/Swiss-Prot),   Q2M3S5 (UniProtKB/Swiss-Prot),   Q9Y5H5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_054724   ⟸   NM_014005
- Peptide Label: isoform 2 precursor
- UniProtKB: Q9Y5H5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000436042   ⟸   ENST00000532602
RefSeq Acc Id: ENSP00000367362   ⟸   ENST00000378122
Protein Domains
Cadherin

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y5H5-F1-model_v2 AlphaFold Q9Y5H5 1-950 view protein structure

Promoters
RGD ID:6870898
Promoter ID:EPDNEW_H8613
Type:initiation region
Name:PCDHA9_1
Description:protocadherin alpha 9
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,848,382 - 140,848,442EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8675 AgrOrtholog
COSMIC PCDHA9 COSMIC
Ensembl Genes ENSG00000204961 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000291657 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000378122 ENTREZGENE
  ENST00000378122.4 UniProtKB/Swiss-Prot
  ENST00000532602 ENTREZGENE
  ENST00000532602.2 UniProtKB/Swiss-Prot
  ENST00000708308.1 UniProtKB/Swiss-Prot
  ENST00000708309.1 UniProtKB/Swiss-Prot
Gene3D-CATH Cadherins UniProtKB/Swiss-Prot
GTEx ENSG00000204961 GTEx
  ENSG00000291657 GTEx
HGNC ID HGNC:8675 ENTREZGENE
Human Proteome Map PCDHA9 Human Proteome Map
InterPro Cadherin-like_dom UniProtKB/Swiss-Prot
  Cadherin-like_sf UniProtKB/Swiss-Prot
  Cadherin_CBD UniProtKB/Swiss-Prot
  Cadherin_CS UniProtKB/Swiss-Prot
  Cadherin_N UniProtKB/Swiss-Prot
KEGG Report hsa:9752 UniProtKB/Swiss-Prot
NCBI Gene 9752 ENTREZGENE
OMIM 606315 OMIM
PANTHER CADHERIN-87A UniProtKB/Swiss-Prot
  PROTOCADHERIN ALPHA-9 UniProtKB/Swiss-Prot
Pfam Cadherin UniProtKB/Swiss-Prot
  Cadherin_2 UniProtKB/Swiss-Prot
  Cadherin_tail UniProtKB/Swiss-Prot
PharmGKB PA33021 PharmGKB
PRINTS CADHERIN UniProtKB/Swiss-Prot
PROSITE CADHERIN_1 UniProtKB/Swiss-Prot
  CADHERIN_2 UniProtKB/Swiss-Prot
SMART SM00112 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF49313 UniProtKB/Swiss-Prot
UniProt O15053 ENTREZGENE
  PCDA9_HUMAN UniProtKB/Swiss-Prot
  Q2M3S5 ENTREZGENE
  Q9Y5H5 ENTREZGENE
UniProt Secondary O15053 UniProtKB/Swiss-Prot
  Q2M3S5 UniProtKB/Swiss-Prot