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Items: 1 to 20 of 142

1.

nsv3877210

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MXD4
Location information:
Clinical significance:
Benign
ID:
48440565
variant
2.

nsv3871725

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MXD4
Location information:
Clinical significance:
Benign
ID:
48435080
variant
3.

nsv3885830

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MXD4
Location information:
Clinical significance:
Benign
ID:
48449185
variant
4.

nsv3879141

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MXD4
Location information:
Clinical significance:
Benign
ID:
48442496
variant
5.

nsv3879921

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZFYVE28
,
MXD4
Location information:
Clinical significance:
Benign
ID:
48443276
variant
6.

nsv3878771

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4800
,
MXD4
Location information:
Clinical significance:
Benign
ID:
48442126
variant
7.

nsv3887436

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZFYVE28
,
MXD4
Location information:
Clinical significance:
Benign
ID:
48450791
variant
8.

nsv3886862

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZFYVE28
,
MXD4
Location information:
Clinical significance:
Benign
ID:
48450217
variant
9.

nsv3873502

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MXD4
,
ZFYVE28
Location information:
Clinical significance:
Benign
ID:
48436857
variant
10.

nsv3886622

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4800
,
MXD4
,
ZFYVE28
Location information:
Clinical significance:
Benign
ID:
48449977
variant
11.

nsv3885103

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COX6B1P5
,
MXD4
,
HAUS3
,
POLN
,
MIR4800
Location information:
Clinical significance:
Benign
ID:
48448458
variant
12.

nsv3881991

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4800
,
MXD4
,
HAUS3
,
COX6B1P5
,
POLN
Location information:
Clinical significance:
Benign
ID:
48445346
variant
13.

nsv3885762

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CD38
,
DEFB131A
,
LOC112268460
,
KRT18P63
,
LINC02270
,
LOC105374341
,
BLOC1S4
,
MRFAP1
,
LOC107986220
,
CLNK
,
MSX1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48449117
variant
14.

nsv3923296

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR7E99P
,
FBXL5
,
RN7SKP170
,
TMEM129
,
SNORA75B
,
LOC105374502
,
PCGF3-AS1
,
LCORL
,
RGS12
,
LOC105374545
,
RN7SL16P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486651
variant
15.

nsv4674378

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
USP17L30
,
LOC100422637
,
USP17L26
,
TRSUP-TTA3-1
,
LINC01587
,
LOC105374482
,
RPL10AP7
,
LOC101928948
,
STX18
,
LOC105374505
,
LOC105374336
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50271203
variant
16.

nsv6315347

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100421802
,
ADRA2C
,
C1QTNF7
,
ZNF732
,
DGKQ
,
TAPT1
,
LOC105374480
,
USP17L22
,
SNRPCP16
,
QDPR
,
OR7E163P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680294
variant
17.

nsv6291097

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374479
,
LOC105374502
,
MIR4274
,
RGS12
,
LOC105374482
,
LOC105374373
,
PCGF3-AS1
,
USP17L30
,
RN7SKP275
,
LOC107986252
,
HAUS3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53636492
variant
18.

nsv3915161

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CTBP1-AS
,
CPZ
,
LOC105374370
,
LOC101929048
,
UNC93B4
,
LOC105374373
,
USP17L25
,
OR7E85P
,
SLC2A9-AS1
,
LOC100286945
,
LOC107986252
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478516
variant
19.

nsv1398080

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL10AP7
,
RPS7P15
,
LOC105374336
,
LOC101928948
,
LOC105374482
,
LOC100422637
,
CPZ
,
MIR4274
,
RN7SKP275
,
CTBP1-AS
,
USP17L25
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
30347743
variant
20.

nsv6112747

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GPR78
,
LOC105374510
,
RNU6-578P
,
OTOP1
,
LOC105374490
,
NKX1-1
,
RN7SKP292
,
TADA2B
,
SORCS2
,
LOC100533734
,
SNORD162
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53150592
variant
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