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Items: 13

1.

nsv3317580

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Genes(s) in region:
RNF32-DT
Location information:
ID:
47177295
variant
2.

nsv3318326

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Genes(s) in region:
ERBB4
Location information:
ID:
47178041
variant
3.

nsv3318323

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Genes(s) in region:
LOC105377514
Location information:
ID:
47178038
variant
4.

nsv3318092

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Genes(s) in region:
TM4SF20
Location information:
ID:
47177807
variant
5.

nsv3318495

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Genes(s) in region:
MRGPRX1
Location information:
ID:
47178210
variant
6.

nsv3318830

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Genes(s) in region:
GRAMD1C
,
CTDNEP1P1
Location information:
ID:
47178545
variant
7.

nsv3318508

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Genes(s) in region:
ATAD3B
,
ATAD3C
Location information:
ID:
47178223
variant
8.

nsv3318042

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Genes(s) in region:
ERVV-1
,
ERVV-2
Location information:
ID:
47177757
variant
9.

nsv3317981

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Location information:
ID:
47177696
variant
10.

nsv3318502

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Location information:
ID:
47178217
variant
11.

nsv3317521

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Location information:
ID:
47177236
variant
12.

nsv3318596

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Location information:
ID:
47178311
variant
13.

nsv3317821

Variant type:
copy number variation
Associated study:
nstd157
Organism:
human
Genes(s) in region:
GUCA1C
,
MORC1
,
DPPA2
,
C3orf85
,
LINC00488
,
BRD7P7
,
MORC1-AS1
,
RNU6-1236P
Location information:
ID:
47177536
variant
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