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GRCh38/hg38 17p13.3(chr17:1119701-1561544)x3 AND See cases

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Nov 26, 2012
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:
RCV000141125.5

Allele description [Variation Report for GRCh38/hg38 17p13.3(chr17:1119701-1561544)x3]

GRCh38/hg38 17p13.3(chr17:1119701-1561544)x3

Genes:
  • ABR:ABR activator of RhoGEF and GTPase [Gene - OMIM - HGNC]
  • ABR-AS1:ABR antisense RNA 1 [Gene - HGNC]
  • LOC130059870:ATAC-STARR-seq lymphoblastoid active region 11443 [Gene]
  • LOC130059871:ATAC-STARR-seq lymphoblastoid active region 11444 [Gene]
  • LOC130059872:ATAC-STARR-seq lymphoblastoid active region 11446 [Gene]
  • LOC130059873:ATAC-STARR-seq lymphoblastoid active region 11447 [Gene]
  • LOC130059876:ATAC-STARR-seq lymphoblastoid active region 11448 [Gene]
  • LOC130059877:ATAC-STARR-seq lymphoblastoid active region 11449 [Gene]
  • LOC130059879:ATAC-STARR-seq lymphoblastoid active region 11450 [Gene]
  • LOC130059880:ATAC-STARR-seq lymphoblastoid active region 11451 [Gene]
  • LOC130059881:ATAC-STARR-seq lymphoblastoid active region 11452 [Gene]
  • LOC130059886:ATAC-STARR-seq lymphoblastoid active region 11453 [Gene]
  • LOC130059874:ATAC-STARR-seq lymphoblastoid silent region 7948 [Gene]
  • LOC130059875:ATAC-STARR-seq lymphoblastoid silent region 7949 [Gene]
  • LOC130059878:ATAC-STARR-seq lymphoblastoid silent region 7954 [Gene]
  • LOC130059882:ATAC-STARR-seq lymphoblastoid silent region 7955 [Gene]
  • LOC130059883:ATAC-STARR-seq lymphoblastoid silent region 7956 [Gene]
  • LOC130059884:ATAC-STARR-seq lymphoblastoid silent region 7957 [Gene]
  • LOC130059885:ATAC-STARR-seq lymphoblastoid silent region 7960 [Gene]
  • CRK:CRK proto-oncogene, adaptor protein [Gene - OMIM - HGNC]
  • LOC129390818:MPRA-validated peak2673 silencer [Gene]
  • LOC129390819:MPRA-validated peak2674 silencer [Gene]
  • PITPNA-AS1:PITPNA antisense RNA 1 [Gene - HGNC]
  • LOC121848004:Sharpr-MPRA regulatory region 14526 [Gene]
  • LOC112529892:Sharpr-MPRA regulatory region 4720 [Gene]
  • BHLHA9:basic helix-loop-helix family member a9 [Gene - OMIM - HGNC]
  • INPP5K:inositol polyphosphate-5-phosphatase K [Gene - OMIM - HGNC]
  • MYO1C:myosin IC [Gene - OMIM - HGNC]
  • PITPNA:phosphatidylinositol transfer protein alpha [Gene - OMIM - HGNC]
  • TRARG1:trafficking regulator of GLUT4 (SLC2A4) 1 [Gene - OMIM - HGNC]
  • YWHAE:tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
17p13.3
Genomic location:
Preferred name:
GRCh38/hg38 17p13.3(chr17:1119701-1561544)x3
HGVS:
  • NC_000017.11:g.(?_1119701)_(1561544_?)dup
  • NC_000017.10:g.(?_1022906)_(1464838_?)dup
  • NC_000017.9:g.(?_969656)_(1411588_?)dup
Links:
dbVar: nssv1608102; dbVar: nsv932509
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
SCV000181996ISCA site 1

See additional submitters

no assertion criteria provided
Likely pathogenic
(Nov 26, 2012) 		unknownclinical 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, SCV000181996.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1human1not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providedDiscovery1not providednot providednot provided

Last Updated: May 7, 2024