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Items: 15

1.

nsv3882037

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ITGA1
,
PELO
Location information:
Clinical significance:
Benign
ID:
48445392
variant
2.

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
3.

nsv3923429

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ISCA1P1
,
LOC643307
,
LOC105378959
,
ITGA1
,
LOC105378979
,
IL6ST-DT
,
PART1
,
LOC105378976
,
LINC02225
,
LRRC70
,
SNX18
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486784
variant
5.

nsv4728831

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986380
,
RPS17P11
,
RPS10P12
,
MOCS2
,
MOCS2-DT
,
PELO
,
LOC202319
,
NDUFS4
,
LINC02105
,
KATNBL1P4
,
LOC107986379
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50372468
variant
6.

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
7.

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
8.

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
9.

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
10.

nsv3920391

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KRT18P56
,
LINC01265
,
RANBP3L
,
RNU6-381P
,
RNU6-1296P
,
LINC02224
,
LOC105378998
,
MIR449C
,
LOC100419851
,
KRT8P31
,
ASS1P9
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483746
variant
11.

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
12.

nsv3874099

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ASS1P9
,
LOC105378961
,
RPS19P4
,
RNA5SP182
,
LOC105378959
,
ITGA1
,
MFSD4BP1
,
RPL13AP13
,
LOC105378965
,
B3GNTL1P1
,
LOC105378962
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48437454
variant
13.

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
15.

nsv4456673

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ITGA2
,
MOCS2-DT
,
MOCS2
,
LOC107986380
,
RPL13AP13
,
ITGA1
,
PELO
,
LOC105378965
,
RPL17P21
,
B3GNTL1P1
Location information:
Clinical significance:
Uncertain significance
ID:
49622308
variant
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