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Items: 12

1.

nsv3877040

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105378061
,
MIR4640
,
FUCA2
,
TRV-CAC9-1
,
MRPL35P1
,
SFT2D1
,
PLN
,
EIF3EP1
,
EEF1E1
,
LOC105375018
,
MTRF1L
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48440395
variant
2.

nsv3879811

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-411P
,
LOC107986611
,
RPL5P18
,
MIR1273C
,
TRQ-TTG3-2
,
BVES
,
RPL12P23
,
LOC100421330
,
LOC105378095
,
OR14J1
,
TRA-TGC6-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443166
variant
3.

nsv3887898

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SOD1P1
,
HLA-DPB1
,
H2AC8
,
RNY3P15
,
FBXO30
,
ZDHHC14
,
LOC105378104
,
ZNF76
,
LOC100507547
,
IL17F
,
SLC35D3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48451253
variant
4.

nsv3889814

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ITPR3
,
HSD17B8
,
TRAM2-AS1
,
RPL12P23
,
LOC100132834
,
LOC105374869
,
MIR548AJ1
,
H2BC4
,
OR2J2
,
BTF3P7
,
TRA-AGC23-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453169
variant
5.

nsv4350067

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HLA-DPB2
,
CIMIP3
,
LY6G5B
,
MEP1A
,
CILK1
,
NCR2
,
SKIC2
,
SNORD52
,
COL19A1
,
CLNS1AP1
,
HLA-DQB1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49344980
variant
6.

nsv3913920

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRR-ACG1-2
,
TMEM217
,
POLR1HASP
,
HLA-DPA3
,
ZNF70P1
,
OR2J3
,
TRMEP1
,
RNY4P10
,
PEX6
,
TRM-CAT4-2
,
LOC112267955
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477275
variant
7.

nsv4675941

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AGER
,
AIF1
,
ATP6V1G2
,
BAK1
,
CFB
,
C2
,
C4A
,
C4B
,
CDSN
,
CLIC1
,
COL11A2
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
50272766
variant
8.

nsv7097426

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LEMD2
,
PSORS1C1
,
HSPE1P11
,
C4B
,
IP6K3
,
PSMB8
,
ILRUN-AS1
,
PPT2
,
SFTA2
,
BTNL2
,
LOC101929309
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
55277615
variant
9.

nsv3870570

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105375002
,
SKIC2
,
LINC01556
,
DDR1
,
TRNAL47P
,
MAS1LP1
,
WASF5P
,
PSORS1C3
,
TRF-GAA1-1
,
PRRC2A
,
OR2B4P
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48433925
variant
12.

nsv3921657

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CLIC1
,
SAPCD1
,
LY6G6F
,
LSM2
,
DDAH2
,
MSH5
,
LY6G6E
,
LY6G6F-LY6G6D
,
NEU1
,
MPIG6B
,
HSPA1B
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48485012
variant
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