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Items: 1 to 20 of 35

1.

nsv4769326

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LAMP3
,
RNA5SP151
,
MCF2L2
,
B3GNT5
,
SNORD3P4
Location information:
Clinical significance:
Pathogenic
ID:
50454296
variant
2.

nsv4452071

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MCF2L2
,
LAMP3
,
MCCC1
,
LOC105374247
,
SNORD3P4
Location information:
Clinical significance:
Uncertain significance
ID:
49617706
variant
3.

nsv3914166

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNORA4
,
RNU6-1105P
,
EIF4A2
,
MIR4448
,
LINC01994
,
HTR3E-AS1
,
KLHL6
,
LOC105374264
,
CLCN2
,
RPL34P10
,
ALG3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477521
variant
4.

nsv3882335

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
VPS8
,
MIR1248
,
B3GNT5
,
LOC105374254
,
PSMD2
,
LOC107986167
,
MASP1
,
RPSAP31
,
LINC02069
,
CLDN16
,
PARL
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48445690
variant
10.

nsv7096553

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DVL3
,
LOC105374247
,
AP2M1
,
SNORA63D
,
HSP90AA5P
,
MCCC1
,
EIF2B5
,
SNHG33
,
KLHL6-AS1
,
EEF1AKMT4
,
POLR2H
,
See more...
Location information:
Clinical significance:
Pathogenic,
Uncertain significance
ID:
55276742
variant
11.

nsv3885606

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-62P
,
SEMA3B-AS1
,
TPRG1
,
ITPR1-DT
,
LOC107986112
,
H3P12
,
NT5DC2
,
OR7E122P
,
SRGAP3
,
C3orf36
,
LOC105377018
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448961
variant
12.

nsv3889228

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB4
,
LOC105374108
,
RPL6P7
,
RNY3P13
,
LINC00960
,
LOC107986110
,
TRH
,
LINC02016
,
LOC105377125
,
ZNF589
,
P2RY1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452583
variant
13.

nsv3880617

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP49
,
DLEC1
,
TFDP2
,
IGF2BP2
,
BTD
,
RBM5-AS1
,
RAB43
,
FANCD2
,
CYB561D2
,
PFN2
,
GPR149
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443972
variant
14.

nsv3918981

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02614
,
LINC02054
,
RNU6-143P
,
SEC62
,
MTCH2P1
,
LOC105374144
,
LOC105374041
,
SLC35G2
,
LOC105374147
,
RAP1BP2
,
LINC01998
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482336
variant
15.

nsv3918692

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374179
,
LINC02038
,
LINC02023
,
WDR49
,
LOC105374153
,
RNU6-507P
,
FGF12-AS1
,
UBQLN4P1
,
LOC105374262
,
XXYLT1
,
LINC02082
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482047
variant
16.

nsv3874894

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-901P
,
LINC02083
,
ASS1P7
,
HTR3C2P
,
LINC02069
,
MAP3K13
,
HNRNPA1P24
,
IGF2BP2-AS1
,
TIPARP-AS1
,
TMEM212
,
DYNLL1P5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438249
variant
17.

nsv3918066

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374260
,
LOC105374174
,
LOC105374280
,
SMCO1
,
RNU6-1279P
,
SNAR-I
,
LOC105374257
,
TMEM212-AS1
,
LINC02029
,
FLJ42393
,
MIR4789
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481421
variant
18.

nsv3918149

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02031
,
PCBP2P4
,
LINC00880
,
RN7SKP296
,
DYNLT2B
,
SNORD3P4
,
RN7SL738P
,
MTHFD2P7
,
LOC105374217
,
SNORA81
,
FXR1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481504
variant
19.

nsv3913128

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNORA4
,
MTCO3P38
,
RPL23AP42
,
RNU6-1233P
,
FAM131A
,
HRG
,
KLHL6
,
TM4SF19-AS1
,
LINC01327
,
MIR6828
,
ACTBP16
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476483
variant
20.

nsv3914686

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL34P10
,
LOC105374264
,
MIR3137
,
GOLIM4
,
MIR551B
,
LOC105374284
,
EIF4A2
,
RPL39P19
,
LOC105374287
,
C9orf85P2
,
RN7SL215P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478041
variant
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