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Items: 9

1.

nsv3889848

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MEGF10
,
LOC100128407
,
RPL36AP20
,
CSNK1A1
,
LOC105374695
,
RPL36AP21
,
RNU4-14P
,
LOC105374672
,
LOC105377715
,
CATSPER2P2
,
LOC101927046
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453203
variant
2.

nsv3886374

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374618
,
HARS1
,
TRQ-CTG13-1
,
GEMIN5
,
GABRG2
,
LOC728575
,
BOLA3P3
,
RPL23AP44
,
SMIM3
,
PRDM6-AS1
,
SLC30A5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48449729
variant
3.

nsv3871533

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PCDHGC5
,
RGS14
,
CDC42SE2
,
MCIDAS
,
TRPC6P2
,
RNA5SP188
,
PCYOX1L
,
LINC01170
,
LOC105377730
,
TNIP1
,
ATG10
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48434888
variant
4.

nsv3875235

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SPEF2
,
NDST1
,
GALNT10
,
MTND5P11
,
CTBP2P4
,
SSBP2
,
PCDHB15
,
SLC2A3P1
,
LOC101927514
,
LINC02058
,
FBXW11
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438590
variant
5.

nsv3911585

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02241
,
ATPSCKMT
,
BTF3
,
IRX1
,
LINC02116
,
PRELID3BP4
,
RPL19P11
,
KRT8P31
,
RN7SL58P
,
SLC6A18
,
SUMO2P4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474940
variant
6.

nsv4675667

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101929380
,
LIX1-AS1
,
RPS23
,
RN7SL814P
,
RNU6-308P
,
LOC105379096
,
NCRUPAR
,
LOC644936
,
CERT1
,
ACTBP2
,
LINC01331
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272492
variant
7.

nsv4436202

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU1-150P
,
RNU6-727P
,
MIR12130
,
TRPC6P2
,
LNPEP
,
RPS17P2
,
ADAMTS6
,
UQCRQ
,
LOC100505796
,
LOC105374719
,
MRPS5P3
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
49579806
variant
8.

nsv3912593

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105378993
,
LOC107986375
,
LOC105379016
,
IRX4
,
PPIGP1
,
CD180
,
CAPSL
,
LOC100130177
,
RETREG1
,
LOC105374702
,
GMCL2
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48475948
variant
9.

nsv4675088

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NSA2
,
RNU7-196P
,
ANKRA2
,
UTP15
,
RN7SL814P
,
LINC02122
,
LINC01333
,
RNU6-1330P
,
HEXB
,
LOC105379035
,
LOC107986423
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50271913
variant
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