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Items: 15

1.

nsv3886606

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNX7
Location information:
Clinical significance:
Uncertain significance
ID:
48449961
variant
2.

nsv3902590

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PLPPR5-AS1
,
PLPPR5
,
SNX7
Location information:
Clinical significance:
Uncertain significance
ID:
48465945
variant
3.

nsv3900925

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNX7
,
PLPPR5-AS1
,
PLPPR5
Location information:
Clinical significance:
Uncertain significance
ID:
48464280
variant
4.

nsv6313675

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01307
,
FTLP17
,
KATNBL1P2
,
UBL4B
,
DPH5-DT
,
LINC01761
,
RNU6-965P
,
LINC01930
,
KCNA10
,
LOC105378899
,
WDR47
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677546
variant
5.

nsv3893941

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPSAP19
,
ATXN7L2
,
NDE1P1
,
MYBPHL
,
GNAT2
,
SLC6A17-AS1
,
LOC105378874
,
LOC107985174
,
RNU4-75P
,
RTCA-AS1
,
MIR2682
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457296
variant
6.

nsv3909776

ID:
48473131
variant
8.

nsv3877365

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MARK1
,
LINC02766
,
FDPS
,
PRUNE1
,
GJB4
,
RN7SL653P
,
PPIEL
,
CRB1
,
SELENBP1
,
LBR
,
CHML
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48440720
variant
9.

nsv3885206

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNAP47
,
STK40
,
RNU6-750P
,
LINC01138
,
MIR4632
,
LOC107985100
,
EIF2D
,
SEPTIN7P13
,
RAB13
,
LOC107985524
,
DR1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448561
variant
10.

nsv3884414

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU1-153P
,
MIR3917
,
LOC105378793
,
CCDC190
,
RPL29P6
,
RUNX3-AS1
,
MIXL1
,
LCE1B
,
NAXE
,
PDC-AS1
,
BNIPL
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447769
variant
11.

nsv3882464

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02607
,
RNVU1-19
,
MIR137HG
,
TLCD4
,
LOC105378901
,
TRN-GTT7-1
,
LOC107985524
,
RN7SKP270
,
LOC646970
,
DNAJA1P5
,
LOC107985447
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48445819
variant
12.

nsv3898327

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01773
,
LOC107985095
,
OLFM3
,
LMO4
,
PKN2-AS1
,
LOC105378835
,
LOC105378838
,
RNU1-130P
,
FEN1P1
,
LRRC39
,
LINC01650
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461682
variant
13.

nsv3884558

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC25A24
,
LOC100271656
,
MIR378G
,
RNPC3
,
GSTM1
,
GSTM3
,
LINC01397
,
CNN3-DT
,
DPYD-AS2
,
PSMA5
,
DNAJA1P5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447913
variant
14.

nsv3906578

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DPYD-AS1
,
PLPPR5-AS1
,
RPL26P9
,
PLPPR5
,
NDUFS5P2
,
EEF1A1P11
,
LOC105378866
,
RPL7P9
,
LOC101060164
,
MIR2682
,
MIR137HG
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48469933
variant
15.

nsv4436181

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01776
,
IGSF21-AS1
,
BRI3P1
,
LINC01635
,
ACOT11
,
RPL23AP17
,
NFYC
,
RPL7L1P22
,
EPHA2-AS1
,
SH3BGRL3
,
ECE1-AS1
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
49579785
variant
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