U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 8

1.

nsv6622122

Variant type:
copy number variation
Associated study:
nstd224
Organism:
human
Genes(s) in region:
SKA3
Location information:
ID:
54336238
variant

2.

nsv6631657

Variant type:
copy number variation
Associated study:
nstd224
Organism:
human
Genes(s) in region:
LOC105375567
,
AOC1
Location information:
ID:
54345773
variant

3.

nsv6630321

Variant type:
copy number variation
Associated study:
nstd224
Organism:
human
Genes(s) in region:
BTNL9
,
MIR8089
Location information:
ID:
54344437
variant

4.

nsv6625164

Variant type:
copy number variation
Associated study:
nstd224
Organism:
human
Genes(s) in region:
PLIN3
,
ARRDC5
Location information:
ID:
54339280
variant

5.

nsv6620485

Variant type:
copy number variation
Associated study:
nstd224
Organism:
human
Genes(s) in region:
AHCYP1
,
ANTXRL
,
ANTXRLP1
,
LOC105378577
Location information:
ID:
54334601
variant

6.

nsv6622759

Variant type:
copy number variation
Associated study:
nstd224
Organism:
human
Genes(s) in region:
NDUFB1
,
ATXN3
,
CPSF2
Location information:
ID:
54336875
variant

7.

nsv6632177

Variant type:
copy number variation
Associated study:
nstd224
Organism:
human
Genes(s) in region:
ZP3
,
POMZP3
,
DTX2
,
FDPSP2
,
LINC03009
,
SPDYE16
,
UPK3B
,
LOC105375358
Location information:
ID:
54346293
variant

8.

nsv6625893

Variant type:
copy number variation
Associated study:
nstd224
Organism:
human
Genes(s) in region:
FCGR2A
,
FCGR3A
,
HSPA6
,
TRG-TCC2-6
,
TRL-CAG1-6
,
TRN-GTT1-1
,
TRG-GCC2-1
,
TRD-GTC10-1
,
RPS23P10
Location information:
ID:
54340009
variant

Format
Items per page

Send to:

Choose Destination

Supplemental Content

Filters: Manage Filters

Find related data

Search details

See more...

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
Support Center