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Items: 1 to 20 of 36

1.

nsv4682039

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Pathogenic
ID:
50284719
variant
2.

nsv5381724

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Pathogenic
ID:
51636981
variant
3.

nsv3874075

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Pathogenic
ID:
48437430
variant
4.

nsv6312787

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Pathogenic
ID:
53676658
variant
5.

nsv3907180

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Pathogenic
ID:
48470535
variant
6.

nsv3872755

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Likely pathogenic
ID:
48436110
variant
7.

nsv6312413

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Likely benign
ID:
53676284
variant
8.

nsv3884151

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Likely benign
ID:
48447506
variant
9.

nsv5980434

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Likely benign
ID:
52885785
variant
10.

nsv4452241

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Uncertain significance
ID:
49617876
variant
11.

nsv7098130

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Uncertain significance
ID:
55278319
variant
12.

nsv7097384

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCTD7
Location information:
Clinical significance:
Uncertain significance
ID:
55277573
variant
13.

nsv6636632

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100996437
,
RABGEF1
,
KCTD7
Location information:
Clinical significance:
Uncertain significance
ID:
54355461
variant
14.

nsv3919826

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-438P
,
LOC105375300
,
URGCP
,
MOXD2P
,
LOC105375171
,
SP4
,
LOC105375194
,
LOC105375277
,
TRBV21-1
,
MIR4283-1
,
VN1R24P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483181
variant
15.

nsv3888815

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986817
,
DNAJB9
,
LRRN3
,
SKAP2
,
LOC107986794
,
MAGI2-AS2
,
CPA2
,
MIR10525
,
VN1R37P
,
SPDYE7P
,
DPY19L1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452170
variant
16.

nsv3917508

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GTF2IP4
,
ZNF680P1
,
FKBP6
,
LOC112267981
,
CRCP
,
HNRNPA1P75
,
LOC346329
,
TNRC18P2
,
LOC102724777
,
LINC01005
,
LINC03006
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480863
variant
18.

nsv3906315

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01372
,
CLUHP7
,
LOC100419781
,
LOC105375330
,
VN1R42P
,
INTS4P1
,
INTS4P2
,
ZNF107
,
RNU6-229P
,
LOC644387
,
LOC107986704
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469670
variant
19.

nsv3894780

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-565P
,
LAMB1
,
MIR5707
,
LOC100419774
,
ZNF786
,
ELK1P1
,
MTCYBP42
,
SSU72L6
,
EEF1A1P27
,
LOC105375200
,
THUMPD3P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458135
variant
20.

nsv4455091

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP51
,
FLJ40288
,
STAG3L2
,
FKBP9
,
BNIP3P11
,
GPR37
,
LOC105375251
,
LOC100419642
,
LOC105375148
,
PMS2P7
,
TRBV10-3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49620726
variant
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