U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 12

1.

nsv997201

Variant type:
copy number variation
Associated study:
nstd45
Organism:
human
Genes(s) in region:
TBX3
,
TBX3-AS1
Location information:
Clinical significance:
Pathogenic
ID:
17336843
variant
2.

nsv3907306

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105369999
,
TBX3-AS1
Location information:
Clinical significance:
Benign
ID:
48470661
variant
3.

nsv1398091

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TBX3
,
TBX3-AS1
Location information:
Clinical significance:
Uncertain significance
ID:
30347754
variant
4.

nsv3890891

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TBX3
,
OSTF1P1
,
TBX3-AS1
,
LOC105369999
Location information:
Clinical significance:
Pathogenic
ID:
48454246
variant
5.

nsv3898489

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OSTF1P1
,
TBX3-AS1
,
TBX3
Location information:
Clinical significance:
Uncertain significance
ID:
48461844
variant
6.

nsv6309391

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105369993
,
MIR6762
,
LOC105369990
,
TBX3
,
IMMP1LP2
,
PLBD2
,
OAS2
,
GLULP5
,
LHX5-AS1
,
SDSL
,
RPH3A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53673262
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.

nsv3913894

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TAOK3
,
LINC02405
,
LOC105370086
,
LOC100419701
,
PUS1
,
LOC105370012
,
RPLP0
,
CCDC92
,
ADGRD1
,
LINC02985
,
SNORA49
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477249
variant
Format
Items per page

Send to:

Choose Destination

Supplemental Content

Find related data

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center