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Items: 1 to 20 of 49

1.

nsv6311973

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC50
Location information:
Clinical significance:
Uncertain significance
ID:
53675844
variant
2.

nsv3884122

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UTS2B
,
CCDC50
Location information:
Clinical significance:
Benign
ID:
48447477
variant
3.

nsv3912740

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC50
,
UTS2B
Location information:
Clinical significance:
Uncertain significance
ID:
48476095
variant
4.

nsv3910370

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC50
,
UTS2B
,
OSTN
,
PYDC2
,
PYDC2-AS1
Location information:
Clinical significance:
Uncertain significance
ID:
48473725
variant
5.

nsv3911287

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC50
,
PYDC2
,
UTS2B
,
PYDC2-AS1
Location information:
Clinical significance:
Uncertain significance
ID:
48474642
variant
6.

nsv4728398

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC50
,
OSTN
,
UTS2B
Location information:
Clinical significance:
Uncertain significance
ID:
50372035
variant
7.

nsv3915488

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNAR-I
,
RPL23AP93
,
RTP1
,
RNU6-821P
,
LINC01983
,
HRG
,
UTS2B
,
PAK2
,
LINC02048
,
SNORA81
,
RN7SKP222
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478843
variant
8.

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
9.

nsv3920607

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FGF12
,
RFC4
,
CRYGS
,
DNAJB11
,
RNU1-20P
,
UTS2B
,
LINC02013
,
SMBD1P
,
ATP13A3
,
LPP
,
LOC105374295
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483962
variant
10.

nsv3872972

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TMEM44
,
CLDN1
,
MIR4797
,
RPL35A
,
MUC4
,
ATP13A3-DT
,
MUC20P1
,
NRROS
,
LOC100129725
,
LOC105374307
,
RN7SL215P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48436327
variant
11.

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
12.

nsv6290259

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01972
,
LINC02026
,
NMNAT1P3
,
ATP13A5
,
RPL36P7
,
SDHAP4
,
RNU6-1101P
,
PYDC2-AS1
,
MIR4797
,
HES1
,
LOC100288016
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53634136
variant
15.

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
16.

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
17.

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
18.

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
19.

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
20.

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
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