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Items: 1 to 20 of 32

1.

nsv4684075

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SEC23B
Location information:
Clinical significance:
Pathogenic
ID:
50286970
variant
2.

nsv4450466

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SEC23B
Location information:
Clinical significance:
Pathogenic
ID:
49616101
variant
3.

nsv7095547

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SEC23B
Location information:
Clinical significance:
Uncertain significance
ID:
55275736
variant
4.

nsv4676419

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PGAM3P
,
EEF1A1P34
,
DZANK1
,
LINC00687
,
ANKEF1
,
RNU6-192P
,
LOC112268271
,
LOC100286962
,
RPS3P1
,
LOC107985384
,
RNU6-115P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50273244
variant
5.

nsv3891787

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CST3
,
CST8
,
NAA20
,
LOC101929707
,
LINC01431
,
RPL41P1
,
CST12P
,
RALGAPA2
,
CST7
,
NKX2-4
,
MED28P7
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455142
variant
7.

nsv3892750

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TGIF2-RAB5IF
,
LOC105372609
,
PGBD4P2
,
DUXAP7
,
SPINT3
,
C20orf144
,
ASIP
,
BMP7-AS1
,
TRPC4AP
,
SHLD1
,
MCM8-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456105
variant
8.

nsv3905072

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LRRN4
,
SNRPB
,
ABHD12
,
SCAND1
,
RPL21P3
,
TGM2
,
RPL37AP1
,
RPS15AP1
,
SCP2D1-AS1
,
TMEM74B
,
PREX1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468427
variant
9.

nsv3895314

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PKIG
,
LINC01523
,
KCNK15-AS1
,
NELFCD
,
PCED1A
,
FAM210B
,
LOC105372492
,
PROCR
,
RPSAP1
,
ANKEF1
,
SPINT4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458669
variant
10.

nsv3896520

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COMMD7
,
RNU7-6P
,
RPL36P1
,
TTLL9
,
LINC01428
,
CD93
,
PARAL1
,
LOC101929863
,
LOC105372655
,
LOC107984001
,
LOC100131496
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48459875
variant
11.

nsv3920218

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR3646
,
NPEPL1
,
LSM14B
,
RNU6-147P
,
RNU6ATAC34P
,
PCIF1
,
SNTA1
,
LOC105376989
,
LOC107985402
,
LOC100289473
,
DLGAP4-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483573
variant
12.

nsv3908959

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ISM1-AS1
,
CST9LP2
,
LOC105372518
,
CRLS1
,
VN1R108P
,
MAVS
,
EEF1A1P34
,
LOC112268271
,
LOC105372521
,
LOC105372492
,
ANKEF1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472314
variant
13.

nsv3913796

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNY4P11
,
EIF4E2P1
,
RNA5SP532
,
PA2G4P2
,
SNAP25-AS1
,
RSPO4
,
PANK2
,
CFAP61
,
MIR3192
,
FRG1DP
,
RARRES2P11
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477151
variant
14.

nsv3922272

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ISM1-AS1
,
CST2
,
CST9LP2
,
LOC105372498
,
RNU6ATAC34P
,
CST11
,
PCNA
,
NXT1
,
CST5
,
FKBP1A
,
PLCB1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485627
variant
15.

nsv3910142

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DYNLRB1
,
LOC107985402
,
OTOR
,
MKKS
,
GLRXP1
,
LOC107987277
,
NANP
,
POFUT1
,
RPL12P3
,
LINC01431
,
RNU1-131P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473497
variant
16.

nsv4349190

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372582
,
LOC101929937
,
CSTP1
,
RPS18P1
,
LOC102606466
,
PYGB
,
SNX5
,
RASSF2
,
CHGB
,
LIN28AP3
,
LOC105372499
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49344103
variant
17.

nsv3919898

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR3192
,
CFAP61
,
CSTP1
,
RSPO4
,
SMOX
,
SEL1L2
,
LINC00237
,
SNORD86
,
FAT1P1
,
MED28P7
,
CST12P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483253
variant
18.

nsv3907558

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC03086
,
RN7SKP69
,
NSFL1C
,
LAMP5
,
LOC105372535
,
LINC01730
,
RNU6-1019P
,
RN7SL14P
,
LOC105372532
,
LOC107985384
,
LOC105372509
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470913
variant
19.

nsv3913704

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NRSN2
,
LOC102724545
,
LOC100419956
,
LOC101929547
,
LOC105372571
,
SNORD110
,
LOC149844
,
LOC105372568
,
LOC105372545
,
LOC105372542
,
SLC23A2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477059
variant
20.

nsv7148267

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KRT18P3
,
RSPO4
,
PANK2
,
RNA5SP474
,
RNA5SP477
,
DEFB125
,
LOC105372547
,
LOC101618237
,
SOX12
,
DUXAP7
,
LOC105372567
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55378183
variant
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