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Items: 1 to 20 of 35

1.

nsv3887969

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GLUL
Location information:
Clinical significance:
Benign
ID:
48451324
variant
2.

nsv3876010

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GLUL
Location information:
Clinical significance:
Benign
ID:
48439365
variant
3.

nsv3912840

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CRB1
,
STX6
,
RPS23P9
,
SLAMF1
,
CRTC2
,
RN7SL372P
,
IL6R
,
RNU6-693P
,
RPL35AP5
,
C1orf105
,
ATP8B2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476195
variant
4.

nsv3874431

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PTGS2
,
RASAL2-AS1
,
SNORD76
,
TOR1AIP2
,
LOC105371661
,
LINC00272
,
SNORD47
,
RNU6-157P
,
CDC73
,
LINC02816
,
RGSL1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437786
variant
5.

nsv3873192

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COLGALT2
,
NOS1AP
,
MR1P1
,
LINC02818
,
MIR556
,
MORF4L1P7
,
NTMT2
,
MIR3119-1
,
LOC107985232
,
RNASEL
,
LINC01688
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48436547
variant
6.

nsv3888143

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CSRP1-AS1
,
EEF1A1P44
,
LOC107985458
,
NPHS2
,
SMG7-AS1
,
LOC105371667
,
LINC01350
,
RNA5SP72
,
COLGALT2
,
LOC647150
,
MR1P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48451498
variant
7.

nsv4673925

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
QSOX1
,
PTPRC
,
TEDDM2P
,
OVAAL
,
FAM163A
,
RPL23AP22
,
HNRNPA1P54
,
LINC01633
,
PRG4
,
RNU7-183P
,
IER5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50270750
variant
8.

nsv3878624

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105371661
,
C1orf53
,
ZBTB41
,
LINC00272
,
LOC105371664
,
LOC100420254
,
RPS3AP9
,
CFHR1
,
ACBD6
,
MEF2AP1
,
F13B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48441979
variant
9.

nsv3905741

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC4A1APP2
,
EEF1A1P44
,
HNRNPA1P46
,
CFHR1
,
TOR1AIP2
,
LOC107985458
,
MEF2AP1
,
CDC73
,
C1orf53
,
ZBTB41
,
EDEM3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469096
variant
10.

nsv3904393

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL18P2
,
KIAA0040
,
MYOC
,
RASAL2
,
TEX50
,
RPL26P11
,
CEP350
,
RPL22P24
,
MCRIP2P2
,
RPSAP16
,
LOC646870
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467748
variant
11.

nsv3877653

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02818
,
LINC01720
,
ZBTB41
,
LOC647150
,
FDPSP1
,
AXDND1
,
HNRNPA1P46
,
EIF1P3
,
SLC4A1APP2
,
LINC01688
,
LOC127011
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48441008
variant
12.

nsv3896481

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL230P
,
RPS27AP5
,
RNU5F-2P
,
IER5
,
RNU6-983P
,
QSOX1
,
RPL23AP22
,
RNU7-183P
,
OVAAL
,
LINC01633
,
MIR12116
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48459836
variant
13.

nsv3901149

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RGSL1
,
RNU6-157P
,
PAPPA2
,
SNORD47
,
VAMP4
,
RALGPS2
,
RASAL2-AS1
,
TRUND-NNN7-1
,
PFN1P1
,
LOC105371655
,
AXDND1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48464504
variant
14.

nsv3886667

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CRYZL2P
,
RABGAP1L-AS1
,
SCARNA3
,
TSEN15
,
PRDX6-AS1
,
ASTN1
,
CLEC20A
,
BRINP2
,
HMCN1
,
LOC105371622
,
NCF2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48450022
variant
15.

nsv6637124

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101928933
,
KIAA1614-AS1
,
RGL1
,
RN7SKP156
,
TPR
,
LINC01732
,
GS1-204I12.4
,
VDAC1P4
,
LOC107985238
,
LOC105371636
,
CEP350
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355953
variant
16.

nsv6290451

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU7-13P
,
LOC105371642
,
GAPDHP75
,
LAMC2
,
RNA5SP69
,
LOC105371648
,
RNA5SP73
,
LAMC1
,
RPS3AP8
,
LOC100129573
,
LINC01701
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53635846
variant
17.

nsv3907850

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100129573
,
KIAA0040
,
RNA5SP69
,
LOC126860
,
RALGPS2-AS1
,
TEDDM1
,
RPSAP16
,
LOC105371636
,
RGL1
,
RPS3AP8
,
RPS14P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471205
variant
18.

nsv4436225

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIAA1614-AS1
,
LOC105371630
,
ABL2
,
LOC107985232
,
GLUL
,
RGS16
,
DHX9-AS1
,
LINC01344
,
LOC100421471
,
LOC101928933
,
GPR52
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49579829
variant
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