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Items: 1 to 20 of 129

1.

nsv3920476

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ANTXRLP1
,
ANTXRL
,
AHCYP1
,
LOC105378577
Location information:
Clinical significance:
Likely benign
ID:
48483831
variant
2.

nsv3885445

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AHCYP1
,
ANTXRL
,
ANTXRLP1
,
LOC105378577
Location information:
Clinical significance:
not provided
ID:
48448800
variant
3.

esv3648516

Variant type:
copy number variation
Associated study:
estd216
Organism:
human
Genes(s) in region:
ANTXRL
,
AHCYP1
,
ANTXRLP1
,
LOC105378577
Location information:
Clinical significance:
not provided
ID:
24503756
variant
4.

nsv7137209

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU7-12P
,
RNU1-65P
,
AGAP6
,
RPL15P13
,
LHPP
,
MTCO2P23
,
CHAT
,
LINC02935
,
XRCC6P1
,
MIR548F1
,
ENTPD1-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55356054
variant
5.

nsv4675455

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MRLN
,
LOC102724778
,
ANK3
,
AGAP14P
,
ANXA2P3
,
SLC16A9
,
LOC105378291
,
LOC105378311
,
FAM21EP
,
PARGP1-AGAP4
,
LOC105378314
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272280
variant
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