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Items: 11

1.

nsv909839

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
CCDC102B
Location information:
ID:
9605732
variant

2.

nsv890342

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
LOC105379235
,
MSRA-DT
Location information:
ID:
9586235
variant

3.

nsv893265

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
CNTNAP3B
,
LOC100420440
Location information:
ID:
9589158
variant

4.

nsv883931

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
HCG4B
,
HLA-K
,
HLA-A
Location information:
ID:
9579824
variant

5.

nsv883833

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
HLA-A
,
DDX39BP1
,
MCCD1P1
,
LOC353008
Location information:
ID:
9579726
variant

6.

nsv893407

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
PGM5
,
TMEM252-DT
,
TMEM252
,
LINC01506
Location information:
ID:
9589300
variant

7.

nsv870705

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
CYP4Z1
,
TUBAP9
,
CYP4A22
Location information:
ID:
9566598
variant

8.

nsv876975

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
FAM86DP
,
LSP1P2
,
LINC02018
,
OR7E55P
,
ENPP7P2
,
ALG1L6P
Location information:
ID:
9572868
variant

9.

nsv908392

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
LRRC37A2
,
ARL17B
,
,
NSF
,
NSFP1
,
RN7SL199P
,
ARL17A
,
FAM215B
Location information:
ID:
9604285
variant

10.

nsv871377

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Genes(s) in region:
CYP4A11
,
CYP4A27P
,
CYP4A43P
,
CYP4A44P
,
CYP4Z2P
,
CYP4X1
,
CYP4A26P
Location information:
ID:
9567270
variant

11.

nsv879070

Variant type:
copy number variation
Associated study:
nstd71
Organism:
human
Location information:
ID:
9574963
variant

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