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Items: 1 to 20 of 32

1.

nsv6637090

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CEP162
,
LINC02857
,
MRAP2
Location information:
Clinical significance:
Uncertain significance
ID:
54355919
variant
2.

nsv3921478

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SPACA1
,
TAF13P1
,
PHIP
,
SRSF12
,
DBIP1
,
CASP8AP2
,
CFAP206
,
LOC100127917
,
RN7SL415P
,
LCAL1
,
IRAK1BP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484833
variant
3.

nsv3923528

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-72P
,
LOC100132830
,
TPT1P6
,
LOC101928936
,
LOC105377896
,
RAB1AP2
,
LOC100131124
,
LOC105377899
,
LOC100421583
,
LOC100133102
,
HSPD1P10
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486883
variant
4.

nsv3914309

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ME1
,
GJB7
,
GJA10
,
PGM3
,
ORC3
,
NDUFA5P9
,
MDN1-AS1
,
LOC644269
,
AKIRIN2
,
LOC101928911
,
SNHG5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477664
variant
8.

nsv3877040

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105378061
,
MIR4640
,
FUCA2
,
TRV-CAC9-1
,
MRPL35P1
,
SFT2D1
,
PLN
,
EIF3EP1
,
EEF1E1
,
LOC105375018
,
MTRF1L
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48440395
variant
9.

nsv3879811

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-411P
,
LOC107986611
,
RPL5P18
,
MIR1273C
,
TRQ-TTG3-2
,
BVES
,
RPL12P23
,
LOC100421330
,
LOC105378095
,
OR14J1
,
TRA-TGC6-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443166
variant
10.

nsv3887898

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SOD1P1
,
HLA-DPB1
,
H2AC8
,
RNY3P15
,
FBXO30
,
ZDHHC14
,
LOC105378104
,
ZNF76
,
LOC100507547
,
IL17F
,
SLC35D3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48451253
variant
11.

nsv3889814

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ITPR3
,
HSD17B8
,
TRAM2-AS1
,
RPL12P23
,
LOC100132834
,
LOC105374869
,
MIR548AJ1
,
H2BC4
,
OR2J2
,
BTF3P7
,
TRA-AGC23-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453169
variant
12.

nsv3919111

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-770P
,
MAP3K5-AS2
,
LOC100129847
,
PRSS35
,
RNU4-72P
,
CD164
,
EEF1A1P36
,
LOC100133102
,
TTK
,
SEC63
,
LINC02534
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482466
variant
13.

nsv6313857

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101928570
,
RNU4-72P
,
RNA5SP210
,
LOC100422453
,
PIMREGP3
,
TMEM30A-DT
,
DOP1A
,
BECN1P2
,
COX7A2
,
LOC105377891
,
HTR1B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677728
variant
14.

nsv3872975

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ME1
,
MTATP6P25
,
MDN1-AS1
,
CASC6
,
RPL7P27
,
CNR1
,
RNU4-70P
,
RIPPLY2
,
MANEA-DT
,
LOC107986619
,
RN7SL643P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48436330
variant
15.

nsv3878881

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNAP91
,
CEP162
,
MRAP2
,
RIPPLY2
,
LOC105377879
,
CYB5R4
,
LINC02857
Location information:
Clinical significance:
Benign
ID:
48442236
variant
16.

nsv3882752

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNAP91
,
RIPPLY2
,
LOC105377879
,
LINC02857
,
MRAP2
,
CEP162
,
CYB5R4
Location information:
Clinical significance:
Benign
ID:
48446107
variant
17.

nsv3873754

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNAP91
,
CEP162
,
LOC105377879
,
LINC02857
,
CYB5R4
,
RIPPLY2
,
MRAP2
Location information:
Clinical significance:
Benign
ID:
48437109
variant
18.

nsv6313778

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CYB5R4
,
SMARCE1P2
,
LINC02857
,
LOC107986621
,
LOC107986620
,
CEP162
,
MRAP2
,
LINC01611
,
LOC107986619
Location information:
Clinical significance:
Uncertain significance
ID:
53677649
variant
19.

nsv6634392

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTHFD2P2
,
RPL7P27
,
RPL17P25
,
MIR4643
,
MTATP6P25
,
C6orf163
,
RN7SL415P
,
NT5E
,
LOC100127917
,
LOC105377869
,
LOC105377909
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
54348695
variant
20.

nsv7097097

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MRAP2
,
LOC107986619
,
TBX18-AS1
,
LINC02535
,
CEP162
,
NT5E
,
LOC107986620
,
LOC100421583
,
LOC105377881
,
LOC100421093
,
SMARCE1P2
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
55277286
variant
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