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Items: 1 to 20 of 44

1.

nsv3921817

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SKP293
,
LOC105374906
,
LOC107986570
,
PRPF4B
,
SUMO2P12
,
SLC35B3
,
FAM50B
,
LOC105374946
,
LINC02525
,
RPL7AP36
,
SCARNA27
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485172
variant
2.

nsv3911792

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SIRT5
,
PKMP5
,
LOC105374911
,
HIVEP1
,
LOC105374931
,
ELOVL2
,
TEX56P
,
LOC105374934
,
PPP1R3G
,
LINC03066
,
SMIM13
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475147
variant
3.

nsv3873362

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100506207
,
HTATSF1P2
,
MRPL48P1
,
GCNT2P1
,
RN7SL352P
,
LOC107986559
,
LOC105374889
,
LOC107986516
,
TUBB2BP1
,
LOC105374929
,
LOC101928047
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48436717
variant
4.

nsv3914068

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SSR1
,
LOC107986560
,
LOC100422564
,
TMEM14B
,
LINC00518
,
LOC101928191
,
AMD1P4
,
PAK1IP1
,
LOC105374910
,
THAP12P5
,
LOC102724096
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477423
variant
5.

nsv3923249

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100506207
,
LOC105374889
,
RN7SL352P
,
LOC107986516
,
SERPINB8P1
,
LOC107986559
,
BPHL
,
BTF3P7
,
LOC105374869
,
DUSP22
,
HMGN2P28
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486604
variant
19.

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
20.

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
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