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Items: 19

1.

nsv3883672

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CDV3
Location information:
Clinical significance:
Benign
ID:
48447027
variant
2.

nsv3877151

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CDV3
Location information:
Clinical significance:
Benign
ID:
48440506
variant
3.

nsv3888870

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CDV3
Location information:
Clinical significance:
Benign
ID:
48452225
variant
4.

nsv3889404

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CDV3
Location information:
Clinical significance:
Benign
ID:
48452759
variant
5.

nsv3920279

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NPHP3-AS1
,
RNA5SP142
,
PIK3CB
,
RPS17P9
,
OR7E129P
,
COL6A5
,
TRMT112P5
,
LOC105374117
,
LOC105374123
,
EEF1A1P25
,
TRPC1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483634
variant
6.

nsv6311770

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HNRNPA1P23
,
MIX23
,
SLC49A4
,
RAB7A
,
MARK2P6
,
DNAJB6P7
,
LOC90246
,
LOC105374115
,
ROPN1B
,
PRR23E
,
GOLGB1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53675641
variant
7.

nsv3921297

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BFSP2
,
YWHAQP6
,
MTCH2P1
,
RPL6P9
,
EIF2AK1P1
,
SPSB4
,
RNY4P4
,
RPL31P23
,
KRT18P35
,
EPHB1
,
GK5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484652
variant
8.

nsv3914757

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CLSTN2-AS1
,
COPB2
,
LOC105374115
,
PRR23C
,
CLDN18
,
SOX14
,
HMGB3P14
,
SNORA58
,
LOC105374132
,
PXYLP1
,
LOC102724068
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478112
variant
9.

nsv6112714

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-789P
,
FAM86HP
,
LOC105374121
,
ACAD9
,
NPHP3-ACAD11
,
RN7SKP212
,
CEP63
,
BCL2L12P1
,
GATA2
,
CRIPTOP6
,
UBA5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53150559
variant
12.

nsv3885606

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-62P
,
SEMA3B-AS1
,
TPRG1
,
ITPR1-DT
,
LOC107986112
,
H3P12
,
NT5DC2
,
OR7E122P
,
SRGAP3
,
C3orf36
,
LOC105377018
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448961
variant
13.

nsv3889228

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB4
,
LOC105374108
,
RPL6P7
,
RNY3P13
,
LINC00960
,
LOC107986110
,
TRH
,
LINC02016
,
LOC105377125
,
ZNF589
,
P2RY1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452583
variant
14.

nsv3880617

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP49
,
DLEC1
,
TFDP2
,
IGF2BP2
,
BTD
,
RBM5-AS1
,
RAB43
,
FANCD2
,
CYB561D2
,
PFN2
,
GPR149
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443972
variant
15.

nsv3918981

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02614
,
LINC02054
,
RNU6-143P
,
SEC62
,
MTCH2P1
,
LOC105374144
,
LOC105374041
,
SLC35G2
,
LOC105374147
,
RAP1BP2
,
LINC01998
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482336
variant
16.

nsv6637156

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
H1-10
,
AADACL2-AS1
,
PHF5AP7
,
LINC02014
,
LOC105374211
,
PPM1L
,
CEP70
,
SLC9A9
,
OTOL1
,
LOC105374128
,
CRADDP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355985
variant
17.

nsv3922717

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR7E53P
,
HSPA8P9
,
H3P12
,
RPS3AP14
,
OR5AC4P
,
RAD51AP1P1
,
ITGB5
,
ZBTB20-AS1
,
RLIG1P2
,
COL6A6
,
CHST2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486072
variant
19.

nsv3920834

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NCK1-DT
,
LOC107986126
,
CRIPTOP6
,
COPB2-DT
,
NUP210P1
,
RNU1-30P
,
FAM86HP
,
GATA2
,
RNU6-789P
,
KBTBD12
,
LINC02021
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48484189
variant
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