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GRCh38/hg38 4p16.3(chr4:51519-1405362)x1 AND See cases

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Dec 22, 2010
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000136895.4

Allele description [Variation Report for GRCh38/hg38 4p16.3(chr4:51519-1405362)x1]

GRCh38/hg38 4p16.3(chr4:51519-1405362)x1

Genes:
  • LOC129991944:ATAC-STARR-seq lymphoblastoid active region 21123 [Gene]
  • LOC129991945:ATAC-STARR-seq lymphoblastoid active region 21124 [Gene]
  • LOC129991946:ATAC-STARR-seq lymphoblastoid active region 21125 [Gene]
  • LOC129991949:ATAC-STARR-seq lymphoblastoid active region 21127 [Gene]
  • LOC129991951:ATAC-STARR-seq lymphoblastoid active region 21129 [Gene]
  • LOC129991954:ATAC-STARR-seq lymphoblastoid active region 21131 [Gene]
  • LOC129991955:ATAC-STARR-seq lymphoblastoid active region 21132 [Gene]
  • LOC129991957:ATAC-STARR-seq lymphoblastoid active region 21134 [Gene]
  • LOC129991959:ATAC-STARR-seq lymphoblastoid active region 21135 [Gene]
  • LOC129991960:ATAC-STARR-seq lymphoblastoid active region 21136 [Gene]
  • LOC129991961:ATAC-STARR-seq lymphoblastoid active region 21137 [Gene]
  • LOC129991964:ATAC-STARR-seq lymphoblastoid active region 21139 [Gene]
  • LOC129991966:ATAC-STARR-seq lymphoblastoid active region 21140 [Gene]
  • LOC129991969:ATAC-STARR-seq lymphoblastoid active region 21141 [Gene]
  • LOC129991970:ATAC-STARR-seq lymphoblastoid active region 21142 [Gene]
  • LOC129991976:ATAC-STARR-seq lymphoblastoid active region 21143 [Gene]
  • LOC129991977:ATAC-STARR-seq lymphoblastoid active region 21145 [Gene]
  • LOC129991978:ATAC-STARR-seq lymphoblastoid active region 21146 [Gene]
  • LOC129991979:ATAC-STARR-seq lymphoblastoid active region 21147 [Gene]
  • LOC129991980:ATAC-STARR-seq lymphoblastoid active region 21148 [Gene]
  • LOC129991982:ATAC-STARR-seq lymphoblastoid active region 21149 [Gene]
  • LOC129991985:ATAC-STARR-seq lymphoblastoid active region 21150 [Gene]
  • LOC129991986:ATAC-STARR-seq lymphoblastoid active region 21151 [Gene]
  • LOC129991987:ATAC-STARR-seq lymphoblastoid active region 21152 [Gene]
  • LOC129991993:ATAC-STARR-seq lymphoblastoid active region 21153 [Gene]
  • LOC129991947:ATAC-STARR-seq lymphoblastoid silent region 15096 [Gene]
  • LOC129991948:ATAC-STARR-seq lymphoblastoid silent region 15097 [Gene]
  • LOC129991950:ATAC-STARR-seq lymphoblastoid silent region 15098 [Gene]
  • LOC129991952:ATAC-STARR-seq lymphoblastoid silent region 15102 [Gene]
  • LOC129991953:ATAC-STARR-seq lymphoblastoid silent region 15103 [Gene]
  • LOC129991956:ATAC-STARR-seq lymphoblastoid silent region 15107 [Gene]
  • LOC129991958:ATAC-STARR-seq lymphoblastoid silent region 15110 [Gene]
  • LOC129991962:ATAC-STARR-seq lymphoblastoid silent region 15111 [Gene]
  • LOC129991963:ATAC-STARR-seq lymphoblastoid silent region 15112 [Gene]
  • LOC129991965:ATAC-STARR-seq lymphoblastoid silent region 15113 [Gene]
  • LOC129991967:ATAC-STARR-seq lymphoblastoid silent region 15114 [Gene]
  • LOC129991968:ATAC-STARR-seq lymphoblastoid silent region 15115 [Gene]
  • LOC129991971:ATAC-STARR-seq lymphoblastoid silent region 15117 [Gene]
  • LOC129991972:ATAC-STARR-seq lymphoblastoid silent region 15118 [Gene]
  • LOC129991973:ATAC-STARR-seq lymphoblastoid silent region 15120 [Gene]
  • LOC129991974:ATAC-STARR-seq lymphoblastoid silent region 15121 [Gene]
  • LOC129991975:ATAC-STARR-seq lymphoblastoid silent region 15122 [Gene]
  • LOC129991981:ATAC-STARR-seq lymphoblastoid silent region 15123 [Gene]
  • LOC129991983:ATAC-STARR-seq lymphoblastoid silent region 15124 [Gene]
  • LOC129991984:ATAC-STARR-seq lymphoblastoid silent region 15125 [Gene]
  • LOC129991988:ATAC-STARR-seq lymphoblastoid silent region 15126 [Gene]
  • LOC129991989:ATAC-STARR-seq lymphoblastoid silent region 15127 [Gene]
  • LOC129991990:ATAC-STARR-seq lymphoblastoid silent region 15128 [Gene]
  • LOC129991991:ATAC-STARR-seq lymphoblastoid silent region 15129 [Gene]
  • LOC129991992:ATAC-STARR-seq lymphoblastoid silent region 15130 [Gene]
  • ATP5ME:ATP synthase membrane subunit e [Gene - OMIM - HGNC]
  • LOC126806942:BRD4-independent group 4 enhancer GRCh37_chr4:1190349-1191548 [Gene]
  • LOC126806943:BRD4-independent group 4 enhancer GRCh37_chr4:1317288-1318487 [Gene]
  • LOC126806939:BRD4-independent group 4 enhancer GRCh37_chr4:581897-583096 [Gene]
  • CTBP1:C-terminal binding protein 1 [Gene - OMIM - HGNC]
  • LOC126806944:CDK7 strongly-dependent group 2 enhancer GRCh37_chr4:1319662-1320861 [Gene]
  • LOC126806940:CDK7 strongly-dependent group 2 enhancer GRCh37_chr4:860125-861324 [Gene]
  • LOC126806941:CDK7 strongly-dependent group 2 enhancer GRCh37_chr4:872957-874156 [Gene]
  • CTBP1-AS:CTBP1 antisense RNA [Gene - HGNC]
  • CTBP1-DT:CTBP1 divergent transcript [Gene - HGNC]
  • NKX1-1:NK1 homeobox 1 [Gene - OMIM - HGNC]
  • LOC126806945:P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:1388225-1389424 [Gene]
  • PCGF3-AS1:PCGF3 antisense RNA 1 [Gene - HGNC]
  • PDE6B-AS1:PDE6B antisense RNA 1 [Gene - HGNC]
  • LOC114004382:Sharpr-MPRA regulatory region 8056 [Gene]
  • UVSSA:UV stimulated scaffold protein A [Gene - OMIM - HGNC]
  • IDUA:alpha-L-iduronidase [Gene - OMIM - HGNC]
  • CPLX1:complexin 1 [Gene - OMIM - HGNC]
  • GAK:cyclin G associated kinase [Gene - OMIM - HGNC]
  • CRIPAK:cysteine rich PAK1 inhibitor [Gene - OMIM - HGNC]
  • DGKQ:diacylglycerol kinase theta [Gene - OMIM - HGNC]
  • FGFRL1:fibroblast growth factor receptor like 1 [Gene - OMIM - HGNC]
  • MAEA:macrophage erythroblast attacher, E3 ubiquitin ligase [Gene - OMIM - HGNC]
  • MIR571:microRNA 571 [Gene - HGNC]
  • MYL5:myosin light chain 5 [Gene - OMIM - HGNC]
  • PIGG:phosphatidylinositol glycan anchor biosynthesis class G [Gene - OMIM - HGNC]
  • PDE6B:phosphodiesterase 6B [Gene - OMIM - HGNC]
  • PCGF3:polycomb group ring finger 3 [Gene - OMIM - HGNC]
  • RNF212:ring finger protein 212 [Gene - OMIM - HGNC]
  • SLC26A1:solute carrier family 26 member 1 [Gene - OMIM - HGNC]
  • SLC49A3:solute carrier family 49 member 3 [Gene - OMIM - HGNC]
  • SPON2:spondin 2 [Gene - OMIM - HGNC]
  • TMEM175:transmembrane protein 175 [Gene - OMIM - HGNC]
  • TMEM271:transmembrane protein 271 [Gene - HGNC]
  • LOC100130872:uncharacterized LOC100130872 [Gene]
  • LOC105374338:uncharacterized LOC105374338 [Gene]
  • LOC105374344:uncharacterized LOC105374344 [Gene]
  • ZNF141:zinc finger protein 141 [Gene - OMIM - HGNC]
  • ZNF595:zinc finger protein 595 [Gene - HGNC]
  • ZNF718:zinc finger protein 718 [Gene - HGNC]
  • ZNF721:zinc finger protein 721 [Gene - HGNC]
  • ZNF732:zinc finger protein 732 [Gene - HGNC]
Variant type:
copy number loss
Cytogenetic location:
4p16.3
Genomic location:
Preferred name:
GRCh38/hg38 4p16.3(chr4:51519-1405362)x1
HGVS:
  • NC_000004.12:g.(?_51519)_(1405362_?)del
  • NC_000004.10:g.(?_41413)_(1389150_?)del
  • NC_000004.11:g.(?_51413)_(1399150_?)del
Links:
dbVar: nssv582810; dbVar: nsv534253
Observations:
1

Condition(s)

Name:
See cases [See the Variation display for details]
Identifiers:

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000177030ISCA site 1

See additional submitters

no assertion criteria provided
Pathogenic
(Dec 22, 2010) 		not providedclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
humannot providedyes1not providednot providednot providednot providedclinical testing

Citations

PubMed

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla JA, Eichler EE, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RM, Lee C, Ostell JM, Rosenberg C, et al.

Am J Hum Genet. 2010 May 14;86(5):749-64. doi: 10.1016/j.ajhg.2010.04.006. Review.

PubMed [citation]
PMID:
20466091
PMCID:
PMC2869000

Details of each submission

From ISCA site 1, SCV000177030.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1human1not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1not providedyesnot providednot providedDiscovery1not providednot providednot provided

Last Updated: Oct 14, 2023