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Items: 1 to 20 of 21

1.

nsv3914342

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SKP46
,
VEPH1
,
SLC66A1L
Location information:
Clinical significance:
Likely benign
ID:
48477697
variant
2.

nsv6290244

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC102724145
,
C3orf80
,
HNRNPA1P20
,
LOC101928166
,
LOC105374189
,
LOC105374192
,
LOC105374172
,
LOC107986048
,
LINC02046
,
GM2AP1
,
KPNA4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53634121
variant
3.

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
4.

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
5.

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
6.

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
7.

nsv6637156

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
H1-10
,
AADACL2-AS1
,
PHF5AP7
,
LINC02014
,
LOC105374211
,
PPM1L
,
CEP70
,
SLC9A9
,
OTOL1
,
LOC105374128
,
CRADDP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355985
variant
8.

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
9.

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
10.

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
11.

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
12.

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
13.

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
14.

nsv3918784

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374167
,
LOC105374187
,
LINC01213
,
LOC105374164
,
UC.134
,
LOC105374193
,
LOC105374190
,
TERC
,
RN7SKP298
,
SYPL1P1
,
MTND4LP10
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482139
variant
15.

nsv3889215

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NAALADL2
,
LRRC31
,
TRV-AAC1-1
,
RN7SL229P
,
MLF1-DT
,
LOC105374221
,
LOC112268443
,
TTC14-DT
,
MRPL47
,
RPL35AP10
,
LOC105374224
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452570
variant
16.

nsv5381765

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MBNL1-AS1
,
LOC107986138
,
PLSCR4P1
,
LOC101928236
,
CRADDP1
,
TRIM42
,
RPL21P39
,
TOMM22P6
,
CHST2
,
RPS25P5
,
ARHGEF26-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
51637022
variant
17.

nsv4684209

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTAPP1
,
PLS1
,
PA2G4P4
,
SYPL1P1
,
KPNA4
,
NMD3
,
PLCH1
,
GPR87
,
IFT80
,
C3orf80
,
RBP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50287332
variant
18.

nsv6290273

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02066
,
TM4SF1-AS1
,
SIAH2-AS1
,
RNA5SP146
,
SLC9A9-AS1
,
SAP30P1
,
P2RY12
,
PLSCR5
,
CPA3
,
TM4SF4
,
STRIT1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53634150
variant
19.

nsv6313678

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-901P
,
RPL32P8
,
TIPARP-AS1
,
HNRNPA1P24
,
VEPH1
,
P2RY13
,
DYNLL1P5
,
TMEM183BP
,
RSRC1
,
IGSF10
,
TRIM59
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677549
variant
20.

nsv6313664

ID:
53677535
variant
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