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Items: 11

1.

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
2.

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
3.

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
4.

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
5.

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
6.

nsv4675143

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR6C71P
,
METTL1
,
BLOC1S1-RDH5
,
LRP1-AS
,
PAN2
,
RNU6-879P
,
ZC3H10
,
DCTN2
,
RNU6-279P
,
SPRYD4
,
SHMT2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50271968
variant
8.

nsv6315199

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ERBB3
,
APOF
,
IKZF4
,
LOC107984468
,
MYL6B
,
MIP
,
ANKRD52
,
LOC105369781
,
APONP
,
TRS-CGA4-1
,
SNORD59A
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53680146
variant
9.

nsv6313979

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRS-CGA4-1
,
ANKRD52
,
MIP
,
LOC105369781
,
MYL6B
,
LOC107984468
,
RNU7-40P
,
APONP
,
CNPY2
,
COQ10A
,
RBMS2
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53677850
variant
10.

nsv3893686

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GDF11
,
IKZF4
,
ERBB3
,
ORMDL2
,
LOC105369781
,
MYL6B
,
LOC107984468
,
DNAJC14
,
TMEM198B
,
TRS-CGA4-1
,
MMP19
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48457041
variant
11.

nsv4729160

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS26
,
SUOX
,
LOC105369782
,
MYL6
,
LOC100131294
,
RPL41
,
SMARCC2
,
DGKA
,
MYL6B
,
LOC105369781
,
ERBB3
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50372797
variant
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