SNP Links for Nucleotide (Select 261862244) - SNP

Links from Nucleotide

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Select item 14915714111.

rs1491571411 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: Y:1518438 (GRCh38)
Y:1587332 (GRCh37)
Canonical SPDI:: NC_000024.10:1518438:T:TT
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000017/2 (GnomAD)
HGVS:: NC_000024.10:g.1518439dup, NC_000024.9:g.1587332dup, NG_013252.1:g.23706dup, NC_000023.11:g.1518439dup, NC_000023.10:g.1637332dup

Select item 14915668312.

rs1491566831 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: Y:1460591 (GRCh38)
Y:1529484 (GRCh37)
Canonical SPDI:: NC_000024.10:1460589:TCT:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000017/2 (GnomAD)
-=0.00003/8 (TOPMED)
HGVS:: NC_000024.10:g.1460591_1460592del, NC_000024.9:g.1529484_1529485del, NG_013252.1:g.81554_81555del, NC_000023.11:g.1460591_1460592del, NC_000023.10:g.1579484_1579485del

Select item 14915575293.

rs1491557529 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,AA [Show Flanks]
Chromosome:: Y:1504314 (GRCh38)
Y:1573208 (GRCh37)
Canonical SPDI:: NC_000024.10:1504314::A,NC_000024.10:1504314::AA
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: AA=0.00037/6 (ALFA)
HGVS:: NC_000024.10:g.1504314_1504315insA, NC_000024.10:g.1504314_1504315insAA, NC_000024.9:g.1573207_1573208insA, NC_000024.9:g.1573207_1573208insAA, NG_013252.1:g.37830_37831insT, NG_013252.1:g.37830_37831insTT, NC_000023.11:g.1504314_1504315insA, NC_000023.11:g.1504314_1504315insAA, NC_000023.10:g.1623207_1623208insA, NC_000023.10:g.1623207_1623208insAA

Select item 14915538744.

rs1491553874 has merged into rs1159260456 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: Y:1471322 (GRCh38)
Y:1540215 (GRCh37)
Canonical SPDI:: NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1471309:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: P2RY8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000024.10:g.1471322_1471331del, NC_000024.10:g.1471323_1471331del, NC_000024.10:g.1471324_1471331del, NC_000024.10:g.1471325_1471331del, NC_000024.10:g.1471326_1471331del, NC_000024.10:g.1471327_1471331del, NC_000024.10:g.1471328_1471331del, NC_000024.10:g.1471329_1471331del, NC_000024.10:g.1471330_1471331del, NC_000024.10:g.1471331del, NC_000024.10:g.1471331dup, NC_000024.10:g.1471330_1471331dup, NC_000024.10:g.1471329_1471331dup, NC_000024.10:g.1471328_1471331dup, NC_000024.10:g.1471327_1471331dup, NC_000024.10:g.1471326_1471331dup, NC_000024.10:g.1471325_1471331dup, NC_000024.10:g.1471324_1471331dup, NC_000024.10:g.1471320_1471331dup, NC_000024.10:g.1471319_1471331dup, NC_000024.10:g.1471318_1471331dup, NC_000024.10:g.1471311_1471331dup, NC_000024.10:g.1471310_1471331dup, NC_000024.9:g.1540215_1540224del, NC_000024.9:g.1540216_1540224del, NC_000024.9:g.1540217_1540224del, NC_000024.9:g.1540218_1540224del, NC_000024.9:g.1540219_1540224del, NC_000024.9:g.1540220_1540224del, NC_000024.9:g.1540221_1540224del, NC_000024.9:g.1540222_1540224del, NC_000024.9:g.1540223_1540224del, NC_000024.9:g.1540224del, NC_000024.9:g.1540224dup, NC_000024.9:g.1540223_1540224dup, NC_000024.9:g.1540222_1540224dup, NC_000024.9:g.1540221_1540224dup, NC_000024.9:g.1540220_1540224dup, NC_000024.9:g.1540219_1540224dup, NC_000024.9:g.1540218_1540224dup, NC_000024.9:g.1540217_1540224dup, NC_000024.9:g.1540213_1540224dup, NC_000024.9:g.1540212_1540224dup, NC_000024.9:g.1540211_1540224dup, NC_000024.9:g.1540204_1540224dup, NC_000024.9:g.1540203_1540224dup, NG_013252.1:g.70826_70835del, NG_013252.1:g.70827_70835del, NG_013252.1:g.70828_70835del, NG_013252.1:g.70829_70835del, NG_013252.1:g.70830_70835del, NG_013252.1:g.70831_70835del, NG_013252.1:g.70832_70835del, NG_013252.1:g.70833_70835del, NG_013252.1:g.70834_70835del, NG_013252.1:g.70835del, NG_013252.1:g.70835dup, NG_013252.1:g.70834_70835dup, NG_013252.1:g.70833_70835dup, NG_013252.1:g.70832_70835dup, NG_013252.1:g.70831_70835dup, NG_013252.1:g.70830_70835dup, NG_013252.1:g.70829_70835dup, NG_013252.1:g.70828_70835dup, NG_013252.1:g.70824_70835dup, NG_013252.1:g.70823_70835dup, NG_013252.1:g.70822_70835dup, NG_013252.1:g.70815_70835dup, NG_013252.1:g.70814_70835dup, NC_000023.11:g.1471322_1471331del, NC_000023.11:g.1471323_1471331del, NC_000023.11:g.1471324_1471331del, NC_000023.11:g.1471325_1471331del, NC_000023.11:g.1471326_1471331del, NC_000023.11:g.1471327_1471331del, NC_000023.11:g.1471328_1471331del, NC_000023.11:g.1471329_1471331del, NC_000023.11:g.1471330_1471331del, NC_000023.11:g.1471331del, NC_000023.11:g.1471331dup, NC_000023.11:g.1471330_1471331dup, NC_000023.11:g.1471329_1471331dup, NC_000023.11:g.1471328_1471331dup, NC_000023.11:g.1471327_1471331dup, NC_000023.11:g.1471326_1471331dup, NC_000023.11:g.1471325_1471331dup, NC_000023.11:g.1471324_1471331dup, NC_000023.11:g.1471320_1471331dup, NC_000023.11:g.1471319_1471331dup, NC_000023.11:g.1471318_1471331dup, NC_000023.11:g.1471311_1471331dup, NC_000023.11:g.1471310_1471331dup, NC_000023.10:g.1590215_1590224del, NC_000023.10:g.1590216_1590224del, NC_000023.10:g.1590217_1590224del, NC_000023.10:g.1590218_1590224del, NC_000023.10:g.1590219_1590224del, NC_000023.10:g.1590220_1590224del, NC_000023.10:g.1590221_1590224del, NC_000023.10:g.1590222_1590224del, NC_000023.10:g.1590223_1590224del, NC_000023.10:g.1590224del, NC_000023.10:g.1590224dup, NC_000023.10:g.1590223_1590224dup, NC_000023.10:g.1590222_1590224dup, NC_000023.10:g.1590221_1590224dup, NC_000023.10:g.1590220_1590224dup, NC_000023.10:g.1590219_1590224dup, NC_000023.10:g.1590218_1590224dup, NC_000023.10:g.1590217_1590224dup, NC_000023.10:g.1590213_1590224dup, NC_000023.10:g.1590212_1590224dup, NC_000023.10:g.1590211_1590224dup, NC_000023.10:g.1590204_1590224dup, NC_000023.10:g.1590203_1590224dup

Select item 14915439235.

rs1491543923 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACC,TCC [Show Flanks]
Chromosome:: Y:1461161 (GRCh38)
Y:1530055 (GRCh37)
Canonical SPDI:: NC_000024.10:1461161:CC:CCACC,NC_000024.10:1461161:CC:CCTCC
Validated:: by frequency,by alfa,by cluster
MAF:: CCTCC=0./0 (ALFA)
HGVS:: NC_000024.10:g.1461163_1461164insACC, NC_000024.10:g.1461163_1461164insTCC, NC_000024.9:g.1530056_1530057insACC, NC_000024.9:g.1530056_1530057insTCC, NG_013252.1:g.80983_80984insTGG, NG_013252.1:g.80983_80984insAGG, NC_000023.11:g.1461163_1461164insACC, NC_000023.11:g.1461163_1461164insTCC, NC_000023.10:g.1580056_1580057insACC, NC_000023.10:g.1580056_1580057insTCC

Select item 14915264476.

rs1491526447 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G,GG,GGG,GGGG [Show Flanks]
Chromosome:: Y:1515947 (GRCh38)
Y:1584841 (GRCh37)
Canonical SPDI:: NC_000024.10:1515947:GGGGGG:GGGGGGG,NC_000024.10:1515947:GGGGGG:GGGGGGGG,NC_000024.10:1515947:GGGGGG:GGGGGGGGG,NC_000024.10:1515947:GGGGGG:GGGGGGGGGG
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGGG=0./0 (ALFA)
G=0.00556/73 (TOMMO)
HGVS:: NC_000024.10:g.1515953dup, NC_000024.10:g.1515952_1515953dup, NC_000024.10:g.1515951_1515953dup, NC_000024.10:g.1515950_1515953dup, NC_000024.9:g.1584846dup, NC_000024.9:g.1584845_1584846dup, NC_000024.9:g.1584844_1584846dup, NC_000024.9:g.1584843_1584846dup, NG_013252.1:g.26197dup, NG_013252.1:g.26196_26197dup, NG_013252.1:g.26195_26197dup, NG_013252.1:g.26194_26197dup, NC_000023.11:g.1515953dup, NC_000023.11:g.1515952_1515953dup, NC_000023.11:g.1515951_1515953dup, NC_000023.11:g.1515950_1515953dup, NC_000023.10:g.1634846dup, NC_000023.10:g.1634845_1634846dup, NC_000023.10:g.1634844_1634846dup, NC_000023.10:g.1634843_1634846dup

Select item 14915116987.

rs1491511698 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GA [Show Flanks]
Chromosome:: Y:1497222 (GRCh38)
Y:1566116 (GRCh37)
Canonical SPDI:: NC_000024.10:1497222:A:AGA
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: AGA=0./0 (ALFA)
AG=0.000011/3 (TOPMED)
HGVS:: NC_000024.10:g.1497223_1497224insGA, NC_000024.9:g.1566116_1566117insGA, NG_013252.1:g.44922_44923insCT, NC_000023.11:g.1497223_1497224insGA, NC_000023.10:g.1616116_1616117insGA

Select item 14915093078.

rs1491509307 has merged into rs771296428 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGTGTGTGTGTGTG>-,TG,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTG [Show Flanks]
Chromosome:: Y:1488751 (GRCh38)
Y:1557644 (GRCh37)
Canonical SPDI:: NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000024.10:1488733:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Gene:: P2RY8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTGTGTGTGTGTGTGTG=0./0 (ALFA)
GT=0.3134/1183 (1000Genomes)
HGVS:: NC_000024.10:g.1488735TG[8], NC_000024.10:g.1488735TG[9], NC_000024.10:g.1488735TG[10], NC_000024.10:g.1488735TG[11], NC_000024.10:g.1488735TG[12], NC_000024.10:g.1488735TG[13], NC_000024.10:g.1488735TG[14], NC_000024.10:g.1488735TG[16], NC_000024.10:g.1488735TG[17], NC_000024.10:g.1488735TG[18], NC_000024.10:g.1488735TG[19], NC_000024.10:g.1488735TG[20], NC_000024.10:g.1488735TG[21], NC_000024.10:g.1488735TG[22], NC_000024.9:g.1557628TG[8], NC_000024.9:g.1557628TG[9], NC_000024.9:g.1557628TG[10], NC_000024.9:g.1557628TG[11], NC_000024.9:g.1557628TG[12], NC_000024.9:g.1557628TG[13], NC_000024.9:g.1557628TG[14], NC_000024.9:g.1557628TG[16], NC_000024.9:g.1557628TG[17], NC_000024.9:g.1557628TG[18], NC_000024.9:g.1557628TG[19], NC_000024.9:g.1557628TG[20], NC_000024.9:g.1557628TG[21], NC_000024.9:g.1557628TG[22], NG_013252.1:g.53382AC[8], NG_013252.1:g.53382AC[9], NG_013252.1:g.53382AC[10], NG_013252.1:g.53382AC[11], NG_013252.1:g.53382AC[12], NG_013252.1:g.53382AC[13], NG_013252.1:g.53382AC[14], NG_013252.1:g.53382AC[16], NG_013252.1:g.53382AC[17], NG_013252.1:g.53382AC[18], NG_013252.1:g.53382AC[19], NG_013252.1:g.53382AC[20], NG_013252.1:g.53382AC[21], NG_013252.1:g.53382AC[22], NC_000023.11:g.1488735TG[8], NC_000023.11:g.1488735TG[9], NC_000023.11:g.1488735TG[10], NC_000023.11:g.1488735TG[11], NC_000023.11:g.1488735TG[12], NC_000023.11:g.1488735TG[13], NC_000023.11:g.1488735TG[14], NC_000023.11:g.1488735TG[16], NC_000023.11:g.1488735TG[17], NC_000023.11:g.1488735TG[18], NC_000023.11:g.1488735TG[19], NC_000023.11:g.1488735TG[20], NC_000023.11:g.1488735TG[21], NC_000023.11:g.1488735TG[22], NC_000023.10:g.1607628TG[8], NC_000023.10:g.1607628TG[9], NC_000023.10:g.1607628TG[10], NC_000023.10:g.1607628TG[11], NC_000023.10:g.1607628TG[12], NC_000023.10:g.1607628TG[13], NC_000023.10:g.1607628TG[14], NC_000023.10:g.1607628TG[16], NC_000023.10:g.1607628TG[17], NC_000023.10:g.1607628TG[18], NC_000023.10:g.1607628TG[19], NC_000023.10:g.1607628TG[20], NC_000023.10:g.1607628TG[21], NC_000023.10:g.1607628TG[22]

Select item 14915081749.

rs1491508174 has merged into rs1161266886 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: Y:1539064 (GRCh38)
Y:1607957 (GRCh37)
Canonical SPDI:: NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000024.10:1539050:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: P2RY8 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.000023/6 (TOPMED)
HGVS:: NC_000024.10:g.1539064_1539070del, NC_000024.10:g.1539065_1539070del, NC_000024.10:g.1539066_1539070del, NC_000024.10:g.1539067_1539070del, NC_000024.10:g.1539068_1539070del, NC_000024.10:g.1539069_1539070del, NC_000024.10:g.1539070del, NC_000024.10:g.1539070dup, NC_000024.10:g.1539069_1539070dup, NC_000024.10:g.1539068_1539070dup, NC_000024.10:g.1539067_1539070dup, NC_000024.10:g.1539066_1539070dup, NC_000024.10:g.1539062_1539070dup, NC_000024.10:g.1539061_1539070dup, NC_000024.10:g.1539060_1539070dup, NC_000024.9:g.1607957_1607963del, NC_000024.9:g.1607958_1607963del, NC_000024.9:g.1607959_1607963del, NC_000024.9:g.1607960_1607963del, NC_000024.9:g.1607961_1607963del, NC_000024.9:g.1607962_1607963del, NC_000024.9:g.1607963del, NC_000024.9:g.1607963dup, NC_000024.9:g.1607962_1607963dup, NC_000024.9:g.1607961_1607963dup, NC_000024.9:g.1607960_1607963dup, NC_000024.9:g.1607959_1607963dup, NC_000024.9:g.1607955_1607963dup, NC_000024.9:g.1607954_1607963dup, NC_000024.9:g.1607953_1607963dup, NG_013252.1:g.3088_3094del, NG_013252.1:g.3089_3094del, NG_013252.1:g.3090_3094del, NG_013252.1:g.3091_3094del, NG_013252.1:g.3092_3094del, NG_013252.1:g.3093_3094del, NG_013252.1:g.3094del, NG_013252.1:g.3094dup, NG_013252.1:g.3093_3094dup, NG_013252.1:g.3092_3094dup, NG_013252.1:g.3091_3094dup, NG_013252.1:g.3090_3094dup, NG_013252.1:g.3086_3094dup, NG_013252.1:g.3085_3094dup, NG_013252.1:g.3084_3094dup, NC_000023.11:g.1539064_1539070del, NC_000023.11:g.1539065_1539070del, NC_000023.11:g.1539066_1539070del, NC_000023.11:g.1539067_1539070del, NC_000023.11:g.1539068_1539070del, NC_000023.11:g.1539069_1539070del, NC_000023.11:g.1539070del, NC_000023.11:g.1539070dup, NC_000023.11:g.1539069_1539070dup, NC_000023.11:g.1539068_1539070dup, NC_000023.11:g.1539067_1539070dup, NC_000023.11:g.1539066_1539070dup, NC_000023.11:g.1539062_1539070dup, NC_000023.11:g.1539061_1539070dup, NC_000023.11:g.1539060_1539070dup, NC_000023.10:g.1657957_1657963del, NC_000023.10:g.1657958_1657963del, NC_000023.10:g.1657959_1657963del, NC_000023.10:g.1657960_1657963del, NC_000023.10:g.1657961_1657963del, NC_000023.10:g.1657962_1657963del, NC_000023.10:g.1657963del, NC_000023.10:g.1657963dup, NC_000023.10:g.1657962_1657963dup, NC_000023.10:g.1657961_1657963dup, NC_000023.10:g.1657960_1657963dup, NC_000023.10:g.1657959_1657963dup, NC_000023.10:g.1657955_1657963dup, NC_000023.10:g.1657954_1657963dup, NC_000023.10:g.1657953_1657963dup

Select item 149149829510.

rs1491498295 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: Y:1471309 (GRCh38)
Y:1540202 (GRCh37)
Canonical SPDI:: NC_000024.10:1471308:AT:
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.0172/204 (ALFA)
-=0.02505/1653 (GnomAD)
HGVS:: NC_000024.10:g.1471309_1471310del, NC_000024.9:g.1540202_1540203del, NG_013252.1:g.70835_70836del, NC_000023.11:g.1471309_1471310del, NC_000023.10:g.1590202_1590203del

Select item 149149412911.

rs1491494129 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>-,ATAT [Show Flanks]
Chromosome:: Y:1534150 (GRCh38)
Y:1603043 (GRCh37)
Canonical SPDI:: NC_000024.10:1534143:ATATATAT:ATATAT,NC_000024.10:1534143:ATATATAT:ATATATATAT
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATAT=0.00005/1 (ALFA)
HGVS:: NC_000024.10:g.1534144AT[3], NC_000024.10:g.1534144AT[5], NC_000024.9:g.1603037AT[3], NC_000024.9:g.1603037AT[5], NG_013252.1:g.7994AT[3], NG_013252.1:g.7994AT[5], NC_000023.11:g.1534144AT[3], NC_000023.11:g.1534144AT[5], NC_000023.10:g.1653037AT[3], NC_000023.10:g.1653037AT[5]

Select item 149147955512.

rs1491479555 [Homo sapiens]

Variant type:: INS
Alleles:: ->CTACAGTCCACCCAG [Show Flanks]
Chromosome:: Y:1495590 (GRCh38)
Y:1564484 (GRCh37)
Canonical SPDI:: NC_000024.10:1495590::CTACAGTCCACCCAG
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.1495590_1495591insCTACAGTCCACCCAG, NC_000024.9:g.1564483_1564484insCTACAGTCCACCCAG, NG_013252.1:g.46554_46555insCTGGGTGGACTGTAG, NC_000023.11:g.1495590_1495591insCTACAGTCCACCCAG, NC_000023.10:g.1614483_1614484insCTACAGTCCACCCAG

Select item 149147688313.

rs1491476883 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AC,CAC,CCGC,CGC,CTC,GC [Show Flanks]
Chromosome:: Y:1461170 (GRCh38)
Y:1530064 (GRCh37)
Canonical SPDI:: NC_000024.10:1461170:C:CAC,NC_000024.10:1461170:C:CCAC,NC_000024.10:1461170:C:CCCGC,NC_000024.10:1461170:C:CCGC,NC_000024.10:1461170:C:CCTC,NC_000024.10:1461170:C:CGC
Validated:: by frequency,by alfa,by cluster
MAF:: CCAC=0./0 (ALFA)
HGVS:: NC_000024.10:g.1461171_1461172insAC, NC_000024.10:g.1461171_1461172insCAC, NC_000024.10:g.1461171_1461172insCCGC, NC_000024.10:g.1461171_1461172insCGC, NC_000024.10:g.1461171_1461172insCTC, NC_000024.10:g.1461171_1461172insGC, NC_000024.9:g.1530064_1530065insAC, NC_000024.9:g.1530064_1530065insCAC, NC_000024.9:g.1530064_1530065insCCGC, NC_000024.9:g.1530064_1530065insCGC, NC_000024.9:g.1530064_1530065insCTC, NC_000024.9:g.1530064_1530065insGC, NG_013252.1:g.80974_80975insTG, NG_013252.1:g.80974_80975insTGG, NG_013252.1:g.80974_80975insCGGG, NG_013252.1:g.80974_80975insCGG, NG_013252.1:g.80974_80975insAGG, NG_013252.1:g.80974_80975insCG, NC_000023.11:g.1461171_1461172insAC, NC_000023.11:g.1461171_1461172insCAC, NC_000023.11:g.1461171_1461172insCCGC, NC_000023.11:g.1461171_1461172insCGC, NC_000023.11:g.1461171_1461172insCTC, NC_000023.11:g.1461171_1461172insGC, NC_000023.10:g.1580064_1580065insAC, NC_000023.10:g.1580064_1580065insCAC, NC_000023.10:g.1580064_1580065insCCGC, NC_000023.10:g.1580064_1580065insCGC, NC_000023.10:g.1580064_1580065insCTC, NC_000023.10:g.1580064_1580065insGC

Select item 149147380914.

rs1491473809 has merged into rs1163534557 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,TT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: Y:1521046 (GRCh38)
Y:1589939 (GRCh37)
Canonical SPDI:: NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:1521034:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: P2RY8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000024.10:g.1521046_1521053del, NC_000024.10:g.1521048_1521053del, NC_000024.10:g.1521051_1521053del, NC_000024.10:g.1521052_1521053del, NC_000024.10:g.1521053del, NC_000024.10:g.1521053dup, NC_000024.10:g.1521052_1521053dup, NC_000024.10:g.1521051_1521053dup, NC_000024.10:g.1521050_1521053dup, NC_000024.10:g.1521049_1521053dup, NC_000024.10:g.1521048_1521053dup, NC_000024.10:g.1521047_1521053dup, NC_000024.10:g.1521046_1521053dup, NC_000024.10:g.1521045_1521053dup, NC_000024.10:g.1521044_1521053dup, NC_000024.10:g.1521042_1521053dup, NC_000024.10:g.1521041_1521053dup, NC_000024.10:g.1521036_1521053dup, NC_000024.9:g.1589939_1589946del, NC_000024.9:g.1589941_1589946del, NC_000024.9:g.1589944_1589946del, NC_000024.9:g.1589945_1589946del, NC_000024.9:g.1589946del, NC_000024.9:g.1589946dup, NC_000024.9:g.1589945_1589946dup, NC_000024.9:g.1589944_1589946dup, NC_000024.9:g.1589943_1589946dup, NC_000024.9:g.1589942_1589946dup, NC_000024.9:g.1589941_1589946dup, NC_000024.9:g.1589940_1589946dup, NC_000024.9:g.1589939_1589946dup, NC_000024.9:g.1589938_1589946dup, NC_000024.9:g.1589937_1589946dup, NC_000024.9:g.1589935_1589946dup, NC_000024.9:g.1589934_1589946dup, NC_000024.9:g.1589929_1589946dup, NG_013252.1:g.21103_21110del, NG_013252.1:g.21105_21110del, NG_013252.1:g.21108_21110del, NG_013252.1:g.21109_21110del, NG_013252.1:g.21110del, NG_013252.1:g.21110dup, NG_013252.1:g.21109_21110dup, NG_013252.1:g.21108_21110dup, NG_013252.1:g.21107_21110dup, NG_013252.1:g.21106_21110dup, NG_013252.1:g.21105_21110dup, NG_013252.1:g.21104_21110dup, NG_013252.1:g.21103_21110dup, NG_013252.1:g.21102_21110dup, NG_013252.1:g.21101_21110dup, NG_013252.1:g.21099_21110dup, NG_013252.1:g.21098_21110dup, NG_013252.1:g.21093_21110dup, NC_000023.11:g.1521046_1521053del, NC_000023.11:g.1521048_1521053del, NC_000023.11:g.1521051_1521053del, NC_000023.11:g.1521052_1521053del, NC_000023.11:g.1521053del, NC_000023.11:g.1521053dup, NC_000023.11:g.1521052_1521053dup, NC_000023.11:g.1521051_1521053dup, NC_000023.11:g.1521050_1521053dup, NC_000023.11:g.1521049_1521053dup, NC_000023.11:g.1521048_1521053dup, NC_000023.11:g.1521047_1521053dup, NC_000023.11:g.1521046_1521053dup, NC_000023.11:g.1521045_1521053dup, NC_000023.11:g.1521044_1521053dup, NC_000023.11:g.1521042_1521053dup, NC_000023.11:g.1521041_1521053dup, NC_000023.11:g.1521036_1521053dup, NC_000023.10:g.1639939_1639946del, NC_000023.10:g.1639941_1639946del, NC_000023.10:g.1639944_1639946del, NC_000023.10:g.1639945_1639946del, NC_000023.10:g.1639946del, NC_000023.10:g.1639946dup, NC_000023.10:g.1639945_1639946dup, NC_000023.10:g.1639944_1639946dup, NC_000023.10:g.1639943_1639946dup, NC_000023.10:g.1639942_1639946dup, NC_000023.10:g.1639941_1639946dup, NC_000023.10:g.1639940_1639946dup, NC_000023.10:g.1639939_1639946dup, NC_000023.10:g.1639938_1639946dup, NC_000023.10:g.1639937_1639946dup, NC_000023.10:g.1639935_1639946dup, NC_000023.10:g.1639934_1639946dup, NC_000023.10:g.1639929_1639946dup

Select item 149143724615.

rs1491437246 [Homo sapiens]

Variant type:: DELINS
Alleles:: AC>- [Show Flanks]
Chromosome:: Y:1500011 (GRCh38)
Y:1568904 (GRCh37)
Canonical SPDI:: NC_000024.10:1500009:CAC:C
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.0005/2 (ALFA)
-=0.00025/17 (GnomAD)
-=0.00028/5 (TOMMO)
HGVS:: NC_000024.10:g.1500011_1500012del, NC_000024.9:g.1568904_1568905del, NG_013252.1:g.42134_42135del, NC_000023.11:g.1500011_1500012del, NC_000023.10:g.1618904_1618905del

Select item 149142972316.

rs1491429723 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: Y:1468758 (GRCh38)
Y:1537652 (GRCh37)
Canonical SPDI:: NC_000024.10:1468758::T
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.002525/1 (GnomAD)
HGVS:: NC_000024.10:g.1468758_1468759insT, NC_000024.9:g.1537651_1537652insT, NG_013252.1:g.73386_73387insA, NC_000023.11:g.1468758_1468759insT, NC_000023.10:g.1587651_1587652insT

Select item 149142961717.

rs1491429617 [Homo sapiens]

Variant type:: DEL
Alleles:: CG>- [Show Flanks]
Chromosome:: Y:1515947 (GRCh38)
Y:1584840 (GRCh37)
Canonical SPDI:: NC_000024.10:1515946:CG:
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00015/11 (GnomAD)
HGVS:: NC_000024.10:g.1515947_1515948del, NC_000024.9:g.1584840_1584841del, NG_013252.1:g.26197_26198del, NC_000023.11:g.1515947_1515948del, NC_000023.10:g.1634840_1634841del

Select item 149142328618.

rs1491423286 has merged into rs1452320657 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGGGTGG>-,GTGG,GTGGGTGGGTGG [Show Flanks]
Chromosome:: Y:1473541 (GRCh38)
Y:1542434 (GRCh37)
Canonical SPDI:: NC_000024.10:1473533:TGGGTGGGTGGGTGG:TGGGTGG,NC_000024.10:1473533:TGGGTGGGTGGGTGG:TGGGTGGGTGG,NC_000024.10:1473533:TGGGTGGGTGGGTGG:TGGGTGGGTGGGTGGGTGG
Gene:: P2RY8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGGGTGGGTGGGTGGGTGG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
TGGG=0.000061/1 (TOMMO)
HGVS:: NC_000024.10:g.1473537GTGG[1], NC_000024.10:g.1473537GTGG[2], NC_000024.10:g.1473537GTGG[4], NC_000024.9:g.1542430GTGG[1], NC_000024.9:g.1542430GTGG[2], NC_000024.9:g.1542430GTGG[4], NG_013252.1:g.68600CCCA[1], NG_013252.1:g.68600CCCA[2], NG_013252.1:g.68600CCCA[4], NC_000023.11:g.1473537GTGG[1], NC_000023.11:g.1473537GTGG[2], NC_000023.11:g.1473537GTGG[4], NC_000023.10:g.1592430GTGG[1], NC_000023.10:g.1592430GTGG[2], NC_000023.10:g.1592430GTGG[4]

Select item 149142265919.

rs1491422659 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: Y:1540219 (GRCh38)
Y:1609112 (GRCh37)
Canonical SPDI:: NC_000024.10:1540218:CA:
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000024.10:g.1540219_1540220del, NC_000024.9:g.1609112_1609113del, NG_013252.1:g.1925_1926del, NC_000023.11:g.1540219_1540220del, NC_000023.10:g.1659112_1659113del

Select item 149141775820.

rs1491417758 has merged into rs56347942 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCC>-,C,CC,CCCC,CCCCC,CCCCCC,CCCCCCC,CCCCCCCC,CCCCCCCCC [Show Flanks]
Chromosome:: Y:1461169 (GRCh38)
Y:1530062 (GRCh37)
Canonical SPDI:: NC_000024.10:1461160:CCCCCCCCCCC:CCCCCCCC,NC_000024.10:1461160:CCCCCCCCCCC:CCCCCCCCC,NC_000024.10:1461160:CCCCCCCCCCC:CCCCCCCCCC,NC_000024.10:1461160:CCCCCCCCCCC:CCCCCCCCCCCC,NC_000024.10:1461160:CCCCCCCCCCC:CCCCCCCCCCCCC,NC_000024.10:1461160:CCCCCCCCCCC:CCCCCCCCCCCCCC,NC_000024.10:1461160:CCCCCCCCCCC:CCCCCCCCCCCCCCC,NC_000024.10:1461160:CCCCCCCCCCC:CCCCCCCCCCCCCCCC,NC_000024.10:1461160:CCCCCCCCCCC:CCCCCCCCCCCCCCCCC
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCCCCCC=0./0 (ALFA)
HGVS:: NC_000024.10:g.1461169_1461171del, NC_000024.10:g.1461170_1461171del, NC_000024.10:g.1461171del, NC_000024.10:g.1461171dup, NC_000024.10:g.1461170_1461171dup, NC_000024.10:g.1461169_1461171dup, NC_000024.10:g.1461168_1461171dup, NC_000024.10:g.1461167_1461171dup, NC_000024.10:g.1461166_1461171dup, NC_000024.9:g.1530062_1530064del, NC_000024.9:g.1530063_1530064del, NC_000024.9:g.1530064del, NC_000024.9:g.1530064dup, NC_000024.9:g.1530063_1530064dup, NC_000024.9:g.1530062_1530064dup, NC_000024.9:g.1530061_1530064dup, NC_000024.9:g.1530060_1530064dup, NC_000024.9:g.1530059_1530064dup, NG_013252.1:g.80982_80984del, NG_013252.1:g.80983_80984del, NG_013252.1:g.80984del, NG_013252.1:g.80984dup, NG_013252.1:g.80983_80984dup, NG_013252.1:g.80982_80984dup, NG_013252.1:g.80981_80984dup, NG_013252.1:g.80980_80984dup, NG_013252.1:g.80979_80984dup, NC_000023.11:g.1461169_1461171del, NC_000023.11:g.1461170_1461171del, NC_000023.11:g.1461171del, NC_000023.11:g.1461171dup, NC_000023.11:g.1461170_1461171dup, NC_000023.11:g.1461169_1461171dup, NC_000023.11:g.1461168_1461171dup, NC_000023.11:g.1461167_1461171dup, NC_000023.11:g.1461166_1461171dup, NC_000023.10:g.1580062_1580064del, NC_000023.10:g.1580063_1580064del, NC_000023.10:g.1580064del, NC_000023.10:g.1580064dup, NC_000023.10:g.1580063_1580064dup, NC_000023.10:g.1580062_1580064dup, NC_000023.10:g.1580061_1580064dup, NC_000023.10:g.1580060_1580064dup, NC_000023.10:g.1580059_1580064dup

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