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Items: 16

1.

nsv6315036

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SETD2
,
KIF9-AS1
Location information:
Clinical significance:
Uncertain significance
ID:
53679442
variant
2.

nsv5381363

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF9-AS1
,
SETD2
Location information:
Clinical significance:
Uncertain significance
ID:
51636620
variant
4.

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
5.

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
6.

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
7.

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
8.

nsv3921797

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RBM5-AS1
,
PRSS42P
,
CYB561D2
,
UCN2
,
TREX1
,
SEMA3F
,
NDUFAF3
,
LINC02019
,
UBA7
,
MON1A
,
RPL17P16
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485152
variant
9.

nsv3883164

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ACAA1
,
ACVR2B
,
AMT
,
APEH
,
RHOA
,
SLC25A20
,
CAMP
,
CCK
,
ENTPD3
,
CDC25A
,
CCR1
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
48446519
variant
10.

nsv4453008

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SCAP
,
SETD2
,
SNORD13P3
,
PTPN23
,
SNORD13J
,
KLHL18
,
KIF9
,
MRPL57P3
,
KIF9-AS1
Location information:
Clinical significance:
Uncertain significance
ID:
49618643
variant
11.

nsv3874579

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PTPN23
,
KLHL18
,
SNORD13J
,
KIF9
,
KIF9-AS1
,
MRPL57P3
,
SCAP
,
SNORD13P3
,
SETD2
Location information:
Clinical significance:
Uncertain significance
ID:
48437934
variant
12.

nsv7097200

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SETD2
,
SNORD13P3
,
KLHL18
,
SNORD13J
,
KIF9
,
PTPN23
,
SCAP
,
KIF9-AS1
Location information:
Clinical significance:
Uncertain significance
ID:
55277389
variant
13.

nsv6637062

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KLHL18
,
SNORD13J
,
KIF9
,
KIF9-AS1
,
SNORD13P3
,
SETD2
Location information:
Clinical significance:
Uncertain significance
ID:
54355891
variant
14.

nsv3918364

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF9
,
KIF9-AS1
,
KLHL18
,
SNORD13J
,
SETD2
,
SNORD13P3
Location information:
Clinical significance:
Uncertain significance
ID:
48481719
variant
15.

nsv6636386

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF9
,
KIF9-AS1
,
SETD2
,
SNORD13P3
,
KLHL18
,
SNORD13J
Location information:
Clinical significance:
Uncertain significance
ID:
54355215
variant
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