U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 11

1.

nsv5380796

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FAUP4
,
MMP7
,
SETP17
,
LUZP2
,
MIR6124
,
KCTD9P4
,
CCND1
,
RNU6-1238P
,
RNA5SP339
,
MMP10
,
GPR152
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
51636053
variant
3.

nsv3893233

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105376598
,
OSBPL9P2
,
LOC100421985
,
NLRP10
,
GLB1L2
,
LINC02685
,
FTH1P16
,
PTS
,
SORL1-AS1
,
OR9G3P
,
OR8G5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456588
variant
4.

nsv3900144

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RTN3
,
KRTAP5-13P
,
LOC653503
,
LOC105376646
,
LOC105369539
,
MPPED2
,
DLG2
,
SORL1-AS1
,
YWHABP2
,
SCN3B
,
TRIM53AP
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463499
variant
5.

nsv3908873

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHMBP2
,
SYTL2
,
LRRC32
,
RPS25
,
OR5AO1P
,
TREHP1
,
OR51A9P
,
CHRNA10
,
BATF2
,
GLYAT
,
PPP2R5B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472228
variant
6.

nsv6315537

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PYGM
,
ATL3
,
LOC105376656
,
LOC649133
,
RPL31P47
,
ALDH3B1
,
RNA5SP350
,
CATSPER1
,
MIR5582
,
MIR192
,
LOC105369571
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680484
variant
7.

nsv3902272

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ACTN3
,
GRK2
,
ARL2
,
BBS1
,
VPS51
,
MRPL49
,
ZNHIT2
,
CAPN1
,
CFL1
,
CST6
,
CTSW
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
48465627
variant
10.

nsv7093694

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
VPS37C
,
POLR2G
,
LOC101927495
,
MIR6747
,
TRPT1
,
MRPL16
,
PLAAT4
,
MS4A4E
,
LINC02705
,
LOC105369339
,
TTC9C
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
55273883
variant
11.

nsv7094093

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
B4GAT1
,
CHKA-DT
,
ALDH3B1
,
DOC2GP
,
CORO1B
,
B4GAT1-DT
,
RNU7-23P
,
UNC93B5
,
MIR6752
,
FOSL1
,
MIR4691
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
55274282
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