U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 29

1.

nsv3880606

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF2A
Location information:
Clinical significance:
Benign
ID:
48443961
variant
2.

nsv3883529

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF2A
Location information:
Clinical significance:
Benign
ID:
48446884
variant
3.

nsv6312112

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF2A
Location information:
Clinical significance:
Uncertain significance
ID:
53675983
variant
4.

nsv6312113

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF2A
,
LOC100421358
Location information:
Clinical significance:
Uncertain significance
ID:
53675984
variant
5.

nsv7096780

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DIMT1
,
KIF2A
Location information:
Clinical significance:
Uncertain significance
ID:
55276969
variant
6.

nsv7096781

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF2A
,
DIMT1
Location information:
Clinical significance:
Uncertain significance
ID:
55276970
variant
7.

nsv6312205

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF2A
,
LOC100421358
,
DIMT1
Location information:
Clinical significance:
Uncertain significance
ID:
53676076
variant
8.

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
9.

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
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.

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
16.

nsv4578696

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRIM23
,
BTF3
,
CCNB1
,
CDH12P2
,
CDK7
,
CFL1P5
,
ERCC8
,
EEF1B2P2
,
FOXD1
,
GTF2H2
,
HTR1A
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
50058446
variant
17.

nsv3883692

ID:
48447047
variant
18.

nsv3880956

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CKS1BP3
,
LRRC70
,
LOC100421358
,
IPO11-LRRC70
,
RNU6-661P
,
KIF2A
,
DIMT1
,
IPO11
,
RPL35AP14
Location information:
Clinical significance:
Benign
ID:
48444311
variant
19.

nsv3884687

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DIMT1
,
IPO11
,
KIF2A
,
CKS1BP3
,
LOC100421358
,
RNU6-661P
Location information:
Clinical significance:
Benign
ID:
48448042
variant
20.

nsv4676090

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IPO11-LRRC70
,
LRRC70
,
LOC100421358
,
RPL35AP14
,
DIMT1
,
RNU6-661P
,
LOC105378998
,
IPO11
,
CKS1BP3
,
KIF2A
,
RN7SKP157
,
See more...
Location information:
Clinical significance:
Likely benign
ID:
50272915
variant
Format
Items per page

Send to:

Choose Destination

Supplemental Content

Find related data

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center