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Items: 12

1.

nsv3905108

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
WIF1
Location information:
Clinical significance:
Benign
ID:
48468463
variant
2.

nsv3907669

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
APOOP3
,
WIF1
,
LEMD3
Location information:
Clinical significance:
Benign
ID:
48471024
variant
3.

nsv6112755

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02421
,
TBC1D15
,
LOC100125409
,
RPL39P28
,
LOC105369828
,
HNRNPA1P70
,
SZRD1P1
,
LOC105369831
,
KCNMB4
,
TBC1D30
,
LOC100509370
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53150600
variant
6.

nsv7094153

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GNS
,
RNU6-166P
,
APOOP3
,
MIR548Z
,
MSRB3
,
WIF1
,
RASSF3-DT
,
TBK1
,
KRT18P60
,
LOC107984522
,
LINC02389
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55274342
variant
7.

nsv3904242

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNA5SP369
,
ST13P22
,
LOC101929432
,
CD63-AS1
,
NCKAP5L
,
RPS20P31
,
LINC02370
,
RNU6-1188P
,
LOC107984486
,
LOC100420442
,
OR6C2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467597
variant
8.

nsv3905447

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOH12CR2
,
OR8S21P
,
RPL21P103
,
LOC105369755
,
SETD1B
,
RNU6-600P
,
LOC105369649
,
NPFF
,
P2RX4
,
MON2
,
LETMD1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468802
variant
9.

nsv3897722

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4ATAC16P
,
PIGAP1
,
RPL21P18
,
RPL41
,
LOC105369976
,
LOC100421618
,
OAS3
,
LINC02417
,
IQSEC3-AS2
,
SLCO1B1
,
DSTNP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461077
variant
10.

nsv3914194

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BTG1P1
,
LOC105370073
,
NRIP2
,
GLTP
,
SMIM10L1
,
RILPL2
,
ANKRD52
,
RPL21P103
,
LOC105369649
,
TMEM119
,
RPL13AP22
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477549
variant
11.

nsv3904719

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR5BT1P
,
RECQL
,
CFAP73
,
A2ML1
,
NENFP2
,
BCAT1
,
SIRT4
,
RPL18P9
,
CCNT1
,
GPD1
,
RNA5SP373
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468074
variant
12.

nsv4674998

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107984522
,
RNU6-166P
,
WIF1
,
APOOP3
,
GNS
,
TBC1D30
,
RPL7P39
,
LEMD3
,
RNU6ATAC42P
,
LINC02389
,
RASSF3
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50271823
variant
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