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GRCh38/hg38 17q21.31(chr17:45578381-46273786)x1 AND See cases

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Feb 18, 2011
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:
RCV000050776.11

Allele description

GRCh38/hg38 17q21.31(chr17:45578381-46273786)x1

Genes:
  • KANSL1-AS1:KANSL1 antisense RNA 1 [Gene - HGNC]
  • KANSL1:KAT8 regulatory NSL complex subunit 1 [Gene - OMIM - HGNC]
  • LINC02210-CRHR1:LINC02210-CRHR1 readthrough [Gene - HGNC]
  • MAPT-AS1:MAPT antisense RNA 1 [Gene - HGNC]
  • MAPT-IT1:MAPT intronic transcript 1 [Gene - HGNC]
  • LOC129390878:MPRA-validated peak2868 silencer [Gene]
  • LOC126862576:P300/CBP strongly-dependent group 1 enhancer GRCh37_chr17:43782244-43783443 [Gene]
  • LOC121852934:Sharpr-MPRA regulatory region 9533 [Gene]
  • CRHR1:corticotropin releasing hormone receptor 1 [Gene - OMIM - HGNC]
  • LRRC37A:leucine rich repeat containing 37A [Gene - OMIM - HGNC]
  • LINC02210:long intergenic non-protein coding RNA 2210 [Gene - HGNC]
  • MAPT:microtubule associated protein tau [Gene - OMIM - HGNC]
  • STH:saitohin [Gene - OMIM - HGNC]
  • SPPL2C:signal peptide peptidase like 2C [Gene - OMIM - HGNC]
Variant type:
copy number loss
Cytogenetic location:
17q21.31
Genomic location:
Preferred name:
GRCh38/hg38 17q21.31(chr17:45578381-46273786)x1
HGVS:
  • NC_000017.11:g.(?_45578381)_(46273786_?)del
  • NC_000017.10:g.(?_43655747)_(44351152_?)del
  • NC_000017.9:g.(?_41011530)_(41706929_?)del
Links:
dbVar: nssv583115; dbVar: nssv706335; dbVar: nssv706374; dbVar: nsv529378
Observations:
3

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
SCV000175310ISCA site 1

See additional submitters

no assertion criteria provided
Pathogenic
(Feb 18, 2011) 		not providedclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providednot providedyes3not 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, SCV000175310.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)
2not provided1not providednot providedclinical testing PubMed (1)
3not provided1not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1not providedyesnot providednot providedDiscovery1not providednot providednot provided
2not providedyesnot providednot providedDiscovery1not providednot providednot provided
3not providedyesnot providednot providedDiscovery1not providednot providednot provided

Last Updated: Oct 14, 2023