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Showing 1-20 of 4,808,335
Variant ID
Variant Type
Organism
Location
Alleles
Method Type
Study
ks620575545 SNV
Homo sapiens
chr16:65325711
( GRCh38 )
C>T
Sequencing
 kstd16
ks620576320 SNV
Homo sapiens
chr16:65818104
( GRCh38 )
A>C
Sequencing
 kstd16
ks620576335 SNV
Homo sapiens
chr16:65830822
( GRCh38 )
T>C
Sequencing
 kstd16
ks620576410 SNV
Homo sapiens
chr16:65869393
( GRCh38 )
C>T
Sequencing
 kstd16
ks620576746 SNV
Homo sapiens
chr16:66009693
( GRCh38 )
G>A
Sequencing
 kstd16
ks620577138 SNV
Homo sapiens
chr16:66217558
( GRCh38 )
C>G
Sequencing
 kstd16
ks620570323 SNV
Homo sapiens
chr16:62979097
( GRCh38 )
C>T
Sequencing
 kstd16
ks620570612 SNV
Homo sapiens
chr16:63108338
( GRCh38 )
C>A
Sequencing
 kstd16
ks620571349 SNV
Homo sapiens
chr16:63434272
( GRCh38 )
A>G
Sequencing
 kstd16
ks620571591 SNV
Homo sapiens
chr16:63542013
( GRCh38 )
T>C
Sequencing
 kstd16
ks620571655 SNV
Homo sapiens
chr16:63562991
( GRCh38 )
T>C
Sequencing
 kstd16
ks620571839 SNV
Homo sapiens
chr16:63661938
( GRCh38 )
T>A
Sequencing
 kstd16
ks616733239 SNV
Homo sapiens
chr2:224894799
( GRCh38 )
C>T
Sequencing
 kstd16
ks616733591 SNV
Homo sapiens
chr2:225062887
( GRCh38 )
T>C
Sequencing
 kstd16
ks616733661 SNV
Homo sapiens
chr2:225089528
( GRCh38 )
A>G
Sequencing
 kstd16
ks616734245 SNV
Homo sapiens
chr2:225279513
( GRCh38 )
G>C
Sequencing
 kstd16
ks620568251 Deletion
Homo sapiens
chr16:62096166
( GRCh38 )
TC>T
Sequencing
 kstd16
ks620568475 Deletion
Homo sapiens
chr16:62170659
( GRCh38 )
TAC>T
Sequencing
 kstd16
ks620569707 SNV
Homo sapiens
chr16:62713981
( GRCh38 )
T>C
Sequencing
 kstd16
ks620569797 SNV
Homo sapiens
chr16:62742024
( GRCh38 )
T>G
Sequencing
 kstd16
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