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Items: 1 to 20 of 183

1.

nsv3919152

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADNP2
Location information:
Clinical significance:
Likely benign
ID:
48482507
variant
2.

nsv3907071

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PARD6G
,
PARD6G-AS1
,
ADNP2
Location information:
Clinical significance:
Benign
ID:
48470426
variant
3.

nsv4457426

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PARD6G-AS1
,
PARD6G
,
ADNP2
Location information:
Clinical significance:
Uncertain significance
ID:
49623061
variant
4.

nsv3910535

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADNP2
,
PARD6G-AS1
,
PARD6G
Location information:
Clinical significance:
Uncertain significance
ID:
48473890
variant
5.

nsv6637560

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TXNL4A
,
ADNP2
,
RBFA
,
SLC66A2
,
PARD6G
,
HSBP1L1
,
PARD6G-AS1
,
SLC25A6P4
,
RBFADN
Location information:
Clinical significance:
Pathogenic
ID:
54356389
variant
6.

nsv3923697

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TXNL4A
,
ADNP2
,
RBFA
,
SLC66A2
,
PARD6G
,
HSBP1L1
,
PARD6G-AS1
,
SLC25A6P4
,
RBFADN
Location information:
Clinical significance:
Pathogenic
ID:
48487052
variant
7.

nsv3902831

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372180
,
MIR4529
,
RNU6-116P
,
LOC105372206
,
ADNP2
,
LOC105372160
,
LOC105372203
,
LOC107985147
,
MEX3C
,
LINC03092
,
MALT1-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466186
variant
8.

nsv3906152

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL17P44
,
LOC100421385
,
LOC105372168
,
ADAD1P2
,
SERPINB8
,
LOC105372191
,
LOC105372188
,
LOC107985172
,
MBD2
,
CPLX4
,
LINC03035
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469507
variant
9.

nsv3909519

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372160
,
LOC105372157
,
RNU6-116P
,
MIR4529
,
LOC105372114
,
LOC105372220
,
MAP1LC3P
,
LOC105372180
,
LOC101927897
,
SINHCAFP2
,
RN7SL795P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472874
variant
10.

nsv3920508

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372152
,
ONECUT2
,
LOC105372212
,
LOC100422053
,
LOC105372169
,
GALR1
,
LOC102725148
,
RNA5SP461
,
LINC01538
,
DIPK1C
,
FAUP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483863
variant
11.

nsv3916196

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372200
,
LOC105372226
,
LINC03092
,
LOC105372120
,
ADNP2
,
LOC105372160
,
MIR4529
,
PMAIP1
,
CCND3P2
,
LOC105372203
,
RN7SL795P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479551
variant
12.

nsv4676105

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR548AV
,
GTSCR1
,
MC4R
,
NEDD4L
,
ATP8B1
,
RPL26P35
,
LINC01909
,
LOC101901828
,
LINC03069
,
LSM6P1
,
HSBP1L1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272930
variant
13.

nsv3914571

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS2P6
,
PARD6G-AS1
,
LINC01929
,
CUPIN1P
,
HMGN1P31
,
RNF152
,
ATP8B1-AS1
,
LINC01909
,
LOC102723506
,
TCF4
,
TSHZ1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477926
variant
14.

nsv3918507

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NETO1
,
SERPINB2
,
LOC100131011
,
MIR5011
,
RNA5SP459
,
POLI
,
LOC339298
,
SERPINB11
,
LOC105372161
,
RNU2-69P
,
ZNF516
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481862
variant
15.

nsv6314216

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNA5SP461
,
CYB5A
,
LOC105372172
,
LOC105376872
,
SALL3
,
CCDC102B
,
CTDP1-DT
,
LINC01538
,
LOC105372146
,
LOC105372152
,
ZNF407-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53678087
variant
16.

nsv3899425

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF236-DT
,
LINC02565
,
LOC107985162
,
RNU2-69P
,
LOC105372221
,
LINC00908
,
LINC01539
,
MIR3591
,
LOC105372141
,
SERPINB11
,
HMSD
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48462780
variant
17.

nsv3918008

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC102725148
,
CCDC102B
,
LINC01538
,
CTDP1-DT
,
ZNF407-AS1
,
LOC107985156
,
LINC01912
,
CYB5A
,
DIPK1C
,
LOC105372132
,
LOC105372152
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481363
variant
18.

nsv3903916

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CBLN2
,
LOC100421257
,
LINC01905
,
LMAN1
,
SERPINB12
,
MALT1-AS1
,
LOC105372203
,
ZNF407
,
LOC105372200
,
LOC105372206
,
LOC105372140
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467271
variant
19.

nsv3900769

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372130
,
RPS3AP49
,
LOC107985177
,
TXNL1
,
ATP8B1-AS1
,
LOC102723506
,
LOC105372156
,
RPL21P126
,
LOC105372213
,
LOC107985134
,
LOC105372170
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48464124
variant
20.

nsv6314188

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF236-DT
,
SERPINB2
,
MIR122
,
RNU2-69P
,
RPL9P31
,
LINC01922
,
SOCS6
,
LINC01029
,
TRG-TCC6-1
,
LOC339298
,
LOC100131011
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53678059
variant
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