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Items: 1 to 20 of 23

1.

nsv3876826

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SEC24A
,
JADE2
,
SAR1B
,
RNU6-1311P
Location information:
Clinical significance:
Likely benign
ID:
48440181
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.

nsv3884357

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TXNDC15
,
PCDHAC1
,
ZMAT2
,
RNU6-482P
,
PCDHB3
,
NCOA4P4
,
LOC101927488
,
ZRSR2P1
,
MIR548P
,
PCDHGA3
,
APBB3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447712
variant
4.

nsv3912937

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01023
,
CTB-99A3.1
,
RPL35AP15
,
LOC105379151
,
CTNNA1-AS1
,
PCDHGC3
,
RN7SKP57
,
SAP30L
,
WDR55
,
ARAP3
,
RPS13P6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476292
variant
5.

nsv3920627

ID:
48483982
variant
11.

nsv3924484

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
C5orf24
,
UBE2B
,
RPS10P11
,
DDX46
,
RPL34P13
,
JADE2
,
CAMLG
,
LOC105379183
,
RPS13P6
,
C5orf15
,
VDAC1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487839
variant
12.

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
13.

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
14.

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
15.

nsv3874238

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PJA2
,
LOC646058
,
PRRC1
,
HTR4
,
HSPD1P18
,
MSX2
,
LINC02147
,
PCDHB15
,
BTNL9
,
CTNNA1-AS1
,
RMND5B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437593
variant
16.

nsv3878636

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100288484
,
IL4
,
PDGFRB
,
ARHGAP26
,
SRA1
,
LOC105378230
,
IL3
,
PCDHGA4
,
RPL36AP20
,
DDX46
,
PCDHGA7
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48441991
variant
17.

nsv3923414

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HNRNPA3P7
,
RNU6-456P
,
RN7SL868P
,
PCDHGA8
,
PCDHB7
,
RPS27AP18
,
RN7SL803P
,
RNU6-1148P
,
LOC112267936
,
PCDHB10
,
PCDHGB8P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486769
variant
18.

nsv3914009

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UQCRQ
,
SNHG4
,
PPP2CA
,
RNA5SP196
,
SPATA24
,
SLC4A9
,
ANKRD49P3
,
KCTD16
,
PCDH12
,
TNIP1
,
GDF9
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477364
variant
19.

nsv3971975

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ACTBP4
,
CAMLG
,
CSF2
,
FBN2
,
GDF9
,
HINT1
,
HSPA4
,
IL3
,
IL4
,
IL5
,
IL9
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
48582992
variant
20.

nsv3884275

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986368
,
PRELID3BP9
,
POGLUT2P1
,
SFXN1
,
RPL35AP16
,
LOC105379151
,
LOC102723654
,
PCDHB2
,
DNAJC18
,
KLF3P1
,
LOC105379174
,
See more...
Location information:
Clinical significance:
Likely benign
ID:
48447630
variant
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