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Items: 1 to 20 of 46

1.

nsv7097689

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COQ4
,
TRUB2
Location information:
Clinical significance:
Uncertain significance
ID:
55277878
variant
9.

nsv3914825

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU7-171P
,
TBC1D13
,
PHYHD1
,
LOC101929270
,
MIR3154
,
LRRC8A
,
SLC25A25-AS1
,
CERCAM
,
ZER1
,
LOC101929291
,
NUP188
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478180
variant
10.

nsv4768374

ID:
50453179
variant
11.

nsv4450425

ID:
49616060
variant
12.

nsv4683557

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SWI5
,
LOC105379841
,
LOC105376286
,
TRR-TCT3-1
,
TMSB4XP4
,
SLC25A25
,
CERCAM
,
PTGES2
,
COQ4
,
TRUB2
,
URM1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50286237
variant
13.

nsv3924593

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LRRC8A
,
SPOUT1
,
RNU7-171P
,
MIR199B
,
LOC105376286
,
SET
,
SWI5
,
ENDOG
,
PKN3
,
MIR219A2
,
RN7SL560P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487948
variant
14.

nsv3912247

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ALOX15P2
,
LOC107987061
,
OR5C1
,
NCLP1
,
FOCAD
,
LOC105375969
,
CDRT15P14
,
TLE4
,
LOC105376184
,
LOC401557
,
LOC105376313
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475602
variant
15.

nsv3890420

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TBC1D13
,
LOC105376186
,
ZDHHC21
,
ZYG11AP1
,
GBGT1
,
VN2R7P
,
PARK7P2
,
ORM1
,
FGF7P6
,
LOC105376292
,
RN7SL544P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453775
variant
16.

nsv3905118

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR219A2
,
CLCN3P1
,
RORB-AS1
,
KLHL9
,
KRT18P24
,
POLR1E
,
CARD19
,
RNU6-1293P
,
RPS2P34
,
NR5A1
,
IL9RP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468473
variant
17.

nsv3891842

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR13C1P
,
CDC37L1
,
IGKV1OR-3
,
NDUFB6
,
GXYLT1P6
,
LOC105375957
,
CAVIN4
,
ACTL7A
,
CYP4F25P
,
MIGA2
,
LOC105379807
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455197
variant
18.

nsv3895453

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL19P15
,
SPATA31D5P
,
PTENP1-AS
,
CARNMT1-AS1
,
MIR4667
,
HSPA5
,
LOC105376020
,
XLOC_007697
,
BSPRY
,
MIR4672
,
LOC107987109
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458808
variant
19.

nsv3900967

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BANCR
,
SETX
,
FBXW2
,
PTGES
,
OR13C5
,
PTENP1
,
CRAT
,
SLC24A2
,
FAM95C
,
LOC105376184
,
ZNG1A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48464322
variant
20.

nsv3907479

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR2AM1P
,
RN7SL565P
,
MIR3689F
,
DOCK8
,
PRSS3
,
MFSD14B
,
MAMDC2-AS1
,
HSPC324
,
COL5A1
,
TMEM203
,
MSANTD3-TMEFF1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470834
variant
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