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GRCh38/hg38 16p11.2(chr16:29581462-30179247)x3 AND See cases

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Feb 15, 2018
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:
RCV000148096.6

Allele description [Variation Report for GRCh38/hg38 16p11.2(chr16:29581462-30179247)x3]

GRCh38/hg38 16p11.2(chr16:29581462-30179247)x3

Genes:
  • LOC130058757:ATAC-STARR-seq lymphoblastoid active region 10657 [Gene]
  • LOC130058760:ATAC-STARR-seq lymphoblastoid active region 10658 [Gene]
  • LOC130058761:ATAC-STARR-seq lymphoblastoid active region 10659 [Gene]
  • LOC130058762:ATAC-STARR-seq lymphoblastoid active region 10660 [Gene]
  • LOC130058763:ATAC-STARR-seq lymphoblastoid active region 10661 [Gene]
  • LOC130058764:ATAC-STARR-seq lymphoblastoid active region 10662 [Gene]
  • LOC130058765:ATAC-STARR-seq lymphoblastoid active region 10663 [Gene]
  • LOC130058766:ATAC-STARR-seq lymphoblastoid active region 10664 [Gene]
  • LOC130058769:ATAC-STARR-seq lymphoblastoid active region 10665 [Gene]
  • LOC130058770:ATAC-STARR-seq lymphoblastoid active region 10667 [Gene]
  • LOC130058772:ATAC-STARR-seq lymphoblastoid active region 10668 [Gene]
  • LOC130058773:ATAC-STARR-seq lymphoblastoid active region 10669 [Gene]
  • LOC130058774:ATAC-STARR-seq lymphoblastoid active region 10670 [Gene]
  • LOC130058775:ATAC-STARR-seq lymphoblastoid active region 10671 [Gene]
  • LOC130058777:ATAC-STARR-seq lymphoblastoid active region 10672 [Gene]
  • LOC130058778:ATAC-STARR-seq lymphoblastoid active region 10673 [Gene]
  • LOC130058780:ATAC-STARR-seq lymphoblastoid active region 10674 [Gene]
  • LOC130058781:ATAC-STARR-seq lymphoblastoid active region 10675 [Gene]
  • LOC130058783:ATAC-STARR-seq lymphoblastoid active region 10676 [Gene]
  • LOC130058787:ATAC-STARR-seq lymphoblastoid active region 10677 [Gene]
  • LOC130058790:ATAC-STARR-seq lymphoblastoid active region 10679 [Gene]
  • LOC130058792:ATAC-STARR-seq lymphoblastoid active region 10680 [Gene]
  • LOC130058793:ATAC-STARR-seq lymphoblastoid active region 10682 [Gene]
  • LOC130058794:ATAC-STARR-seq lymphoblastoid active region 10683 [Gene]
  • LOC130058799:ATAC-STARR-seq lymphoblastoid active region 10684 [Gene]
  • LOC130058802:ATAC-STARR-seq lymphoblastoid active region 10686 [Gene]
  • LOC130058803:ATAC-STARR-seq lymphoblastoid active region 10687 [Gene]
  • LOC130058808:ATAC-STARR-seq lymphoblastoid active region 10688 [Gene]
  • LOC130058810:ATAC-STARR-seq lymphoblastoid active region 10689 [Gene]
  • LOC130058812:ATAC-STARR-seq lymphoblastoid active region 10690 [Gene]
  • LOC130058814:ATAC-STARR-seq lymphoblastoid active region 10691 [Gene]
  • LOC130058815:ATAC-STARR-seq lymphoblastoid active region 10692 [Gene]
  • LOC130058756:ATAC-STARR-seq lymphoblastoid silent region 7326 [Gene]
  • LOC130058758:ATAC-STARR-seq lymphoblastoid silent region 7327 [Gene]
  • LOC130058759:ATAC-STARR-seq lymphoblastoid silent region 7328 [Gene]
  • LOC130058767:ATAC-STARR-seq lymphoblastoid silent region 7329 [Gene]
  • LOC130058768:ATAC-STARR-seq lymphoblastoid silent region 7330 [Gene]
  • LOC130058771:ATAC-STARR-seq lymphoblastoid silent region 7331 [Gene]
  • LOC130058776:ATAC-STARR-seq lymphoblastoid silent region 7332 [Gene]
  • LOC130058779:ATAC-STARR-seq lymphoblastoid silent region 7333 [Gene]
  • LOC130058782:ATAC-STARR-seq lymphoblastoid silent region 7334 [Gene]
  • LOC130058784:ATAC-STARR-seq lymphoblastoid silent region 7335 [Gene]
  • LOC130058785:ATAC-STARR-seq lymphoblastoid silent region 7336 [Gene]
  • LOC130058786:ATAC-STARR-seq lymphoblastoid silent region 7337 [Gene]
  • LOC130058788:ATAC-STARR-seq lymphoblastoid silent region 7338 [Gene]
  • LOC130058789:ATAC-STARR-seq lymphoblastoid silent region 7339 [Gene]
  • LOC130058791:ATAC-STARR-seq lymphoblastoid silent region 7340 [Gene]
  • LOC130058795:ATAC-STARR-seq lymphoblastoid silent region 7341 [Gene]
  • LOC130058796:ATAC-STARR-seq lymphoblastoid silent region 7342 [Gene]
  • LOC130058797:ATAC-STARR-seq lymphoblastoid silent region 7343 [Gene]
  • LOC130058798:ATAC-STARR-seq lymphoblastoid silent region 7344 [Gene]
  • LOC130058800:ATAC-STARR-seq lymphoblastoid silent region 7345 [Gene]
  • LOC130058801:ATAC-STARR-seq lymphoblastoid silent region 7346 [Gene]
  • LOC130058804:ATAC-STARR-seq lymphoblastoid silent region 7347 [Gene]
  • LOC130058805:ATAC-STARR-seq lymphoblastoid silent region 7348 [Gene]
  • LOC130058806:ATAC-STARR-seq lymphoblastoid silent region 7349 [Gene]
  • LOC130058807:ATAC-STARR-seq lymphoblastoid silent region 7350 [Gene]
  • LOC130058809:ATAC-STARR-seq lymphoblastoid silent region 7351 [Gene]
  • LOC130058811:ATAC-STARR-seq lymphoblastoid silent region 7352 [Gene]
  • LOC130058813:ATAC-STARR-seq lymphoblastoid silent region 7356 [Gene]
  • CDIPTOSP:CDIP transferase opposite strand, pseudogene [Gene - HGNC]
  • CDIPT:CDP-diacylglycerol--inositol 3-phosphatidyltransferase [Gene - OMIM - HGNC]
  • LOC116276452:CRISPRi-validated cis-regulatory element chr16.2261 [Gene]
  • HIRIP3:HIRA interacting protein 3 [Gene - OMIM - HGNC]
  • INO80E:INO80 complex subunit E [Gene - HGNC]
  • LOC129390783:MPRA-validated peak2562 silencer [Gene]
  • MVP-DT:MVP divergent transcript [Gene - HGNC]
  • MAZ:MYC associated zinc finger protein [Gene - OMIM - HGNC]
  • PAGR1:PAXIP1 associated glutamate rich protein 1 [Gene - OMIM - HGNC]
  • LOC125146440:Sharpr-MPRA regulatory region 10200 [Gene]
  • LOC125146439:Sharpr-MPRA regulatory region 12104 [Gene]
  • LOC112352679:Sharpr-MPRA regulatory region 12377 [Gene]
  • LOC121847977:Sharpr-MPRA regulatory region 13449 [Gene]
  • LOC121847976:Sharpr-MPRA regulatory region 1439 [Gene]
  • LOC112352680:Sharpr-MPRA regulatory region 6067 [Gene]
  • LOC121587540:Sharpr-MPRA regulatory region 8247 [Gene]
  • LOC125146441:Sharpr-MPRA regulatory region 9068 [Gene]
  • TBX6:T-box transcription factor 6 [Gene - OMIM - HGNC]
  • TAOK2:TAO kinase 2 [Gene - OMIM - HGNC]
  • TLCD3B:TLC domain containing 3B [Gene - OMIM - HGNC]
  • YPEL3-DT:YPEL3 divergent transcript [Gene - HGNC]
  • ALDOA:aldolase, fructose-bisphosphate A [Gene - OMIM - HGNC]
  • ASPHD1:aspartate beta-hydroxylase domain containing 1 [Gene - HGNC]
  • C16orf54:chromosome 16 open reading frame 54 [Gene - HGNC]
  • C16orf92:chromosome 16 open reading frame 92 [Gene - OMIM - HGNC]
  • DOC2A:double C2 domain alpha [Gene - OMIM - HGNC]
  • GDPD3:glycerophosphodiester phosphodiesterase domain containing 3 [Gene - OMIM - HGNC]
  • KIF22:kinesin family member 22 [Gene - OMIM - HGNC]
  • MVP:major vault protein [Gene - OMIM - HGNC]
  • MIR3680-2:microRNA 3680-2 [Gene - HGNC]
  • MAPK3:mitogen-activated protein kinase 3 [Gene - OMIM - HGNC]
  • KCTD13:potassium channel tetramerization domain containing 13 [Gene - OMIM - HGNC]
  • PRRT2:proline rich transmembrane protein 2 [Gene - OMIM - HGNC]
  • PPP4C:protein phosphatase 4 catalytic subunit [Gene - OMIM - HGNC]
  • QPRT:quinolinate phosphoribosyltransferase [Gene - OMIM - HGNC]
  • SEZ6L2:seizure related 6 homolog like 2 [Gene - OMIM - HGNC]
  • SPN:sialophorin [Gene - OMIM - HGNC]
  • TMEM219:transmembrane protein 219 [Gene - OMIM - HGNC]
  • LOC112694756:uncharaterized LOC112694756 [Gene]
  • YPEL3:yippee like 3 [Gene - OMIM - HGNC]
  • ZG16:zymogen granule protein 16 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
16p11.2
Genomic location:
Preferred name:
GRCh38/hg38 16p11.2(chr16:29581462-30179247)x3
HGVS:
  • NC_000016.10:g.(?_29581462)_(30179247_?)dup
  • NC_000016.8:g.(?_29500284)_(30098069_?)dup
  • NC_000016.9:g.(?_29592783)_(30190568_?)dup
Links:
dbVar: nssv579334; dbVar: nsv1067734
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
SCV000190767ISCA site 14
no assertion criteria provided
Pathogenic
(Feb 15, 2018) 		de novoclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedde novoyes1not providednot providednot providednot providedclinical testing

Citations

PubMed

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, Collinson MN, Beal SJ, Ackley T, Pickering DL, Golden DM, Aston E, Whitby H, et al.

Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9.

PubMed [citation]
PMID:
21844811
PMCID:
PMC3661946

Details of each submission

From ISCA site 14, SCV000190767.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

Medical records review was possible in 3 out of 4 cases. Two cases presented with phenotypes correlated with the Decipher and MIM:614671 descriptions. In the third case, the phenotype may be masked by the significant global developmental delay that patient has. In one of the 3 cases reviewed, the CNV gain was maternally inherited, yet the mother has a history of panic and anxiety attacks as well as depression. For the 4th case, medical records were not available, however; the reasons for clinical testing, at age 5 years, were listed as encephalopathy, muscle weakness, and lack of coordination.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1de novoyesnot providednot providedDiscovery1not providednot providednot provided

Last Updated: May 7, 2024