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1.

rs1491580575 has merged into rs55660217 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    CACACACACA>-,CA,CACA,CACACA,CACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA [Show Flanks]
    Chromosome:
    5:99548518 (GRCh38)
    5:98884222 (GRCh37)
    Canonical SPDI:
    NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA
    Gene:
    LINC02113 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    ACACACACACACACA=0./0 (ALFA)
    -=0./0 (KOREAN)
    HGVS:
    2.

    rs1491541311 has merged into rs35601920 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TCTCTCTCTCTC>-,TC,TCTC,TCTCTC,TCTCTCTC,TCTCTCTCTC,TCTCTCTCTCTCTC,TCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC [Show Flanks]
      Chromosome:
      5:99575467 (GRCh38)
      5:98911171 (GRCh37)
      Canonical SPDI:
      NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC
      Gene:
      LINC02113 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      CTCTCTCTCTCTCTC=0./0 (ALFA)
      CT=0.2987/1496 (1000Genomes)
      HGVS:
      NC_000005.10:g.99575455TC[6], NC_000005.10:g.99575455TC[7], NC_000005.10:g.99575455TC[8], NC_000005.10:g.99575455TC[9], NC_000005.10:g.99575455TC[10], NC_000005.10:g.99575455TC[11], NC_000005.10:g.99575455TC[13], NC_000005.10:g.99575455TC[14], NC_000005.10:g.99575455TC[15], NC_000005.10:g.99575455TC[16], NC_000005.10:g.99575455TC[17], NC_000005.10:g.99575455TC[18], NC_000005.10:g.99575455TC[19], NC_000005.10:g.99575455TC[20], NC_000005.10:g.99575455TC[21], NC_000005.10:g.99575455TC[22], NC_000005.10:g.99575455TC[23], NC_000005.9:g.98911159TC[6], NC_000005.9:g.98911159TC[7], NC_000005.9:g.98911159TC[8], NC_000005.9:g.98911159TC[9], NC_000005.9:g.98911159TC[10], NC_000005.9:g.98911159TC[11], NC_000005.9:g.98911159TC[13], NC_000005.9:g.98911159TC[14], NC_000005.9:g.98911159TC[15], NC_000005.9:g.98911159TC[16], NC_000005.9:g.98911159TC[17], NC_000005.9:g.98911159TC[18], NC_000005.9:g.98911159TC[19], NC_000005.9:g.98911159TC[20], NC_000005.9:g.98911159TC[21], NC_000005.9:g.98911159TC[22], NC_000005.9:g.98911159TC[23]
      3.

      rs1491529563 has merged into rs200616095 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        ATATAT>-,ATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATTTTAAAATATATGTATTTTAAAATATATATATATATATATATATATAT [Show Flanks]
        Chromosome:
        5:99541635 (GRCh38)
        5:98877339 (GRCh37)
        Canonical SPDI:
        NC_000005.10:99541626:ATATATATATATAT:ATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATATATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATATATATTTTAAAATATATGTATTTTAAAATATATATATATATATATATATATAT
        Gene:
        LINC02113 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        ATATATATATAT=0./0 (ALFA)
        AT=0.075/3 (GENOME_DK)
        HGVS:
        4.

        rs1491418769 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          ->GT [Show Flanks]
          Chromosome:
          5:99541627 (GRCh38)
          5:98877332 (GRCh37)
          Canonical SPDI:
          NC_000005.10:99541627:T:TGT
          Gene:
          LINC02113 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          TGT=0./0 (ALFA)
          TG=0.000004/1 (TOPMED)
          HGVS:
          5.

          rs1491369328 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            ->CA [Show Flanks]
            Chromosome:
            5:99536643 (GRCh38)
            5:98872348 (GRCh37)
            Canonical SPDI:
            NC_000005.10:99536643:CA:CACA
            Gene:
            LINC02113 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            CACA=0.000084/1 (ALFA)
            CA=0.00015/21 (GnomAD)
            CA=0.001734/29 (TOMMO)
            HGVS:
            6.

            rs1491229787 [Homo sapiens]
              Variant type:
              DEL
              Alleles:
              GC>- [Show Flanks]
              Chromosome:
              5:99536643 (GRCh38)
              5:98872347 (GRCh37)
              Canonical SPDI:
              NC_000005.10:99536642:GC:
              Gene:
              LINC02113 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              -=0./0 (ALFA)
              -=0.000004/1 (TOPMED)
              -=0.000007/1 (GnomAD)
              HGVS:
              7.

              rs1491088698 has merged into rs369399517 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                TATATA>-,TA,TATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA [Show Flanks]
                Chromosome:
                5:99541674 (GRCh38)
                5:98877378 (GRCh37)
                Canonical SPDI:
                NC_000005.10:99541662:ATATATATATATATATA:ATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATATATATATA
                Gene:
                LINC02113 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                ATATATATATATA=0./0 (ALFA)
                ATAT=0.21526/1078 (1000Genomes)
                HGVS:
                8.

                rs1491080097 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  ->GC [Show Flanks]
                  Chromosome:
                  5:99548515 (GRCh38)
                  5:98884220 (GRCh37)
                  Canonical SPDI:
                  NC_000005.10:99548515:C:CGC
                  Gene:
                  LINC02113 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  CGC=0./0 (ALFA)
                  HGVS:
                  9.

                  rs1491014516 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AT>- [Show Flanks]
                    Chromosome:
                    5:99548585 (GRCh38)
                    5:98884289 (GRCh37)
                    Canonical SPDI:
                    NC_000005.10:99548583:TAT:T
                    Gene:
                    LINC02113 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    T=0./0 (ALFA)
                    -=0.00018/3 (TOMMO)
                    HGVS:
                    10.

                    rs1490982358 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>G [Show Flanks]
                      Chromosome:
                      5:99537747 (GRCh38)
                      5:98873451 (GRCh37)
                      Canonical SPDI:
                      NC_000005.10:99537746:A:G
                      Gene:
                      LINC02113 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      G=0./0 (ALFA)
                      HGVS:
                      11.

                      rs1490913394 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>A [Show Flanks]
                        Chromosome:
                        5:99552048 (GRCh38)
                        5:98887752 (GRCh37)
                        Canonical SPDI:
                        NC_000005.10:99552047:G:A
                        Gene:
                        LINC02113 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        A=0./0 (ALFA)
                        HGVS:
                        12.

                        rs1490829190 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>C [Show Flanks]
                          Chromosome:
                          5:99564335 (GRCh38)
                          5:98900039 (GRCh37)
                          Canonical SPDI:
                          NC_000005.10:99564334:G:C
                          Gene:
                          LINC02113 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0./0 (ALFA)
                          C=0.000004/1 (TOPMED)
                          C=0.000007/1 (GnomAD)
                          HGVS:
                          13.

                          rs1490731579 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>G,T [Show Flanks]
                            Chromosome:
                            5:99559598 (GRCh38)
                            5:98895302 (GRCh37)
                            Canonical SPDI:
                            NC_000005.10:99559597:C:G,NC_000005.10:99559597:C:T
                            Gene:
                            LINC02113 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000014/2 (GnomAD)
                            T=0.000068/18 (TOPMED)
                            T=0.000177/3 (TOMMO)
                            T=0.001092/2 (Korea1K)
                            HGVS:
                            14.

                            rs1490680194 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>C [Show Flanks]
                              Chromosome:
                              5:99565386 (GRCh38)
                              5:98901090 (GRCh37)
                              Canonical SPDI:
                              NC_000005.10:99565385:A:C
                              Gene:
                              LINC02113 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              C=0./0 (ALFA)
                              C=0.000004/1 (TOPMED)
                              HGVS:
                              15.

                              rs1490645581 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>C [Show Flanks]
                                Chromosome:
                                5:99546822 (GRCh38)
                                5:98882526 (GRCh37)
                                Canonical SPDI:
                                NC_000005.10:99546821:T:C
                                Gene:
                                LINC02113 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                C=0./0 (ALFA)
                                C=0.000008/2 (TOPMED)
                                C=0.000014/2 (GnomAD)
                                HGVS:
                                16.

                                rs1490593110 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>A,C [Show Flanks]
                                  Chromosome:
                                  5:99558718 (GRCh38)
                                  5:98894422 (GRCh37)
                                  Canonical SPDI:
                                  NC_000005.10:99558717:T:A,NC_000005.10:99558717:T:C
                                  Gene:
                                  LINC02113 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  C=0./0 (ALFA)
                                  C=0.000029/4 (GnomAD)
                                  HGVS:
                                  17.

                                  rs1490589437 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>C,G [Show Flanks]
                                    Chromosome:
                                    5:99572568 (GRCh38)
                                    5:98908272 (GRCh37)
                                    Canonical SPDI:
                                    NC_000005.10:99572567:A:C,NC_000005.10:99572567:A:G
                                    Gene:
                                    LINC02113 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000014/2 (GnomAD)
                                    HGVS:
                                    18.

                                    rs1490577295 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>G [Show Flanks]
                                      Chromosome:
                                      5:99533047 (GRCh38)
                                      5:98868751 (GRCh37)
                                      Canonical SPDI:
                                      NC_000005.10:99533046:C:G
                                      Gene:
                                      LINC02113 (Varview)
                                      Functional Consequence:
                                      upstream_transcript_variant,2KB_upstream_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      G=0./0 (ALFA)
                                      HGVS:
                                      19.

                                      rs1490568123 [Homo sapiens]
                                        Variant type:
                                        SNV:
                                        Alleles:
                                        G>A
                                        Chromosome:
                                        no mapping
                                        Canonical SPDI:
                                        20.

                                        rs1490567363 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>G [Show Flanks]
                                          Chromosome:
                                          5:99560006 (GRCh38)
                                          5:98895710 (GRCh37)
                                          Canonical SPDI:
                                          NC_000005.10:99560005:T:G
                                          Gene:
                                          LINC02113 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          G=0./0 (ALFA)
                                          G=0.000004/1 (TOPMED)
                                          HGVS:

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