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Items: 9

3.

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
4.

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
5.

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
6.

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
7.

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
8.

nsv3909395

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RASSF3
,
MIR548Z
,
RASSF3-DT
,
LOC100420899
,
XPOT
,
TBK1
,
TBC1D30
,
LOC107984521
,
GNS
,
MIR548C
,
RPS11P6
,
See more...
Location information:
Clinical significance:
Benign
ID:
48472750
variant
9.

nsv4681587

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
XPOT
,
LOC100420899
,
TBK1
,
ATP6V1E1P3
,
PABPC1P4
,
KICS2
,
C12orf56
,
RPS11P6
,
RPL36AP41
,
LOC100419700
,
RXYLT1-AS1
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50284267
variant
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