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Items: 1 to 20 of 35

1.

nsv3877669

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCNN2
Location information:
Clinical significance:
Benign
ID:
48441024
variant
2.

nsv3922544

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCNN2
Location information:
Clinical significance:
Uncertain significance
ID:
48485899
variant
3.

nsv3920717

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SKP89
,
KCNN2
Location information:
Clinical significance:
Benign
ID:
48484072
variant
4.

nsv6636644

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCNN2
,
RN7SKP89
Location information:
Clinical significance:
Uncertain significance
ID:
54355473
variant
5.

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
6.

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
7.

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
8.

nsv3915450

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MCTP1
,
LOC102467217
,
LINC02234
,
MTND5P10
,
RNU6-752P
,
MTND3P19
,
MTCYBP40
,
RPL28P3
,
LOC345571
,
LOC101927078
,
LOC100289569
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478805
variant
9.

nsv3916468

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105379149
,
LOC107986365
,
SNCAIP
,
LOC105379126
,
MTATP6P2
,
LOC105379083
,
MTCO1P24
,
DDX43P1
,
LOC345576
,
TICAM2-AS1
,
GRAMD2B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479823
variant
10.

nsv3920768

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC102724720
,
LOC107986388
,
LOC105379109
,
POU5F2
,
HMGN2P27
,
CTNNA1P1
,
RPS3AP21
,
SEMA6A-AS2
,
LOC101927023
,
LOC105379129
,
LVRN
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484123
variant
11.

nsv3872414

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZRSR2P1
,
LOC101930276
,
LINC00492
,
SLC25A46
,
RNU6-482P
,
LINC02148
,
RNA5SP188
,
LOC348958
,
RPS20P3
,
LOC101927488
,
LOC105379136
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48435769
variant
12.

nsv6313580

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FER
,
HMGN1P15
,
ST8SIA4
,
RGMB
,
SNORA13
,
CSNK1A1P3
,
RN7SKP230
,
YTHDF1P1
,
DCP2
,
LOC285638
,
LOC101929710
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677451
variant
13.

nsv3924205

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CSNK1G3
,
EPB41L4A-AS1
,
CCDC112
,
ZRSR2P1
,
LOC105379139
,
LINC02148
,
LOC105379136
,
LMNB1
,
SNX2
,
NREP-AS1
,
RN7SL174P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487560
variant
14.

nsv3923804

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FABP5P6
,
AP3S1
,
LOC105379139
,
LOC105379122
,
TNFAIP8
,
LOC285638
,
CCDC112
,
LOC107986441
,
LOC107986444
,
LOC105379119
,
TMED7
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487159
variant
15.

nsv3910959

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02208
,
LOC105379157
,
ZNF474
,
LOC105379137
,
LMNB1-DT
,
ZNF608
,
LAMTOR3P2
,
HMGB1P22
,
KRT18P16
,
LOC102467216
,
TICAM2-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474314
variant
16.

nsv6637111

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC12A2
,
CCDC192
,
ZNF608
,
RPS2P26
,
LAMTOR3P2
,
ZNF474
,
LMNB1-DT
,
LOC105379137
,
LOC112267949
,
LOC105379134
,
HSD17B4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355940
variant
17.

nsv4456071

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HMGN1P13
,
LOC101927023
,
LINC02215
,
RNU6-644P
,
WDR36
,
RNU6-701P
,
STARD4-AS1
,
NREP
,
TMEM183AP6
,
LOC100129526
,
LOC105379149
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49621706
variant
18.

nsv3874025

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02215
,
SEMA6A
,
CTNNA1P1
,
LOC101927023
,
SNX24
,
RPS3AP21
,
TMEM183AP6
,
RNU6-701P
,
PRDM6-AS1
,
LOC100128407
,
RNU6-644P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437380
variant
19.

nsv3920751

ID:
48484106
variant
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