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Showing 1-20 of 931

Variant ID
Variant Type
Organism
Location
Alleles
Method Type
Study
ks228514 SNV
Homo sapiens
chr1:219174752
( GRCh38 )
C>A
Sequencing
kstd1
ks228515 SNV
Homo sapiens
chr1:219175105
( GRCh38 )
C>A
Sequencing
kstd1
ks228516 SNV
Homo sapiens
chr1:219176470
( GRCh38 )
A>G
Sequencing
kstd1
ks228517 SNV
Homo sapiens
chr1:219177431
( GRCh38 )
A>G
Sequencing
kstd1
ks228518 SNV
Homo sapiens
chr1:219178871
( GRCh38 )
T>C
Sequencing
kstd1
ks228519 SNV
Homo sapiens
chr1:219180931
( GRCh38 )
A>C
Sequencing
kstd1
ks228520 SNV
Homo sapiens
chr1:219184082
( GRCh38 )
A>G
Sequencing
kstd1
ks228521 SNV
Homo sapiens
chr1:219184811
( GRCh38 )
A>G
Sequencing
kstd1
ks228522 SNV
Homo sapiens
chr1:219185432
( GRCh38 )
T>G
Sequencing
kstd1
ks228523 SNV
Homo sapiens
chr1:219185735
( GRCh38 )
A>G
Sequencing
kstd1
ks228524 Insertion
Homo sapiens
chr1:219188681
( GRCh38 )
C>CTT
Sequencing
kstd1
ks228525 Insertion
Homo sapiens
chr1:219190622
( GRCh38 )
T>TAAAAA
Sequencing
kstd1
ks228526 Insertion
Homo sapiens
chr1:219190622
( GRCh38 )
T>TAAAAAAA
Sequencing
kstd1
ks228527 SNV
Homo sapiens
chr1:219191759
( GRCh38 )
A>T
Sequencing
kstd1
ks228528 SNV
Homo sapiens
chr1:219193058
( GRCh38 )
T>G
Sequencing
kstd1
ks228529 Insertion
Homo sapiens
chr1:219193061
( GRCh38 )
G>GC
Sequencing
kstd1
ks228530 SNV
Homo sapiens
chr1:219195027
( GRCh38 )
A>G
Sequencing
kstd1
ks228531 SNV
Homo sapiens
chr1:219196372
( GRCh38 )
A>G
Sequencing
kstd1
ks228532 SNV
Homo sapiens
chr1:219196463
( GRCh38 )
A>G
Sequencing
kstd1
ks228533 SNV
Homo sapiens
chr1:219197724
( GRCh38 )
T>G
Sequencing
kstd1
Filter(3)
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