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Items: 8

1.

nsv4728405

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DOCK3
,
DCAF1
,
MANF
,
RBM15B
Location information:
Clinical significance:
Uncertain significance
ID:
50372042
variant
2.

nsv3912778

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SEMA3G
,
INKA1
,
GNAI2
,
TLR9
,
DOCK3
,
ZMYND10
,
IQCF3
,
LINC02017
,
TWF2
,
NAA80
,
BSN-DT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476133
variant
3.

nsv3885606

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-62P
,
SEMA3B-AS1
,
TPRG1
,
ITPR1-DT
,
LOC107986112
,
H3P12
,
NT5DC2
,
OR7E122P
,
SRGAP3
,
C3orf36
,
LOC105377018
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448961
variant
4.

nsv3889228

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB4
,
LOC105374108
,
RPL6P7
,
RNY3P13
,
LINC00960
,
LOC107986110
,
TRH
,
LINC02016
,
LOC105377125
,
ZNF589
,
P2RY1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452583
variant
5.

nsv3880617

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP49
,
DLEC1
,
TFDP2
,
IGF2BP2
,
BTD
,
RBM5-AS1
,
RAB43
,
FANCD2
,
CYB561D2
,
PFN2
,
GPR149
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443972
variant
6.

nsv4347762

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UQCRC1
,
DHX30
,
IQCF5
,
CELSR3
,
VPS26BP1
,
PRSS50
,
ABHD14A
,
CCDC71
,
TREX1
,
UQCC5
,
CCR1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49342675
variant
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