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Items: 1 to 20 of 745

1.

rs1490352778 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>G [Show Flanks]
    Chromosome:
    6:31621149 (GRCh38)
    6:31588926 (GRCh37)
    Canonical SPDI:
    NC_000006.12:31621148:T:G
    Gene:
    PRRC2A (Varview), SNORA38 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0./0 (ALFA)
    G=0.000021/3 (GnomAD)
    G=0.00003/8 (TOPMED)
    ...more
    HGVS:
    2.
    3.

    rs1488221650 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>A,G,T [Show Flanks]
      Chromosome:
      6:31621624 (GRCh38)
      6:31589401 (GRCh37)
      Canonical SPDI:
      NC_000006.12:31621623:C:A,NC_000006.12:31621623:C:G,NC_000006.12:31621623:C:T
      Gene:
      PRRC2A (Varview), SNORA38 (Varview)
      Functional Consequence:
      2KB_upstream_variant,upstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0./0 (ALFA)
      T=0.000014/2 (GnomAD)
      T=0.00067/3 (Estonian)
      ...more
      HGVS:
      4.

      rs1487123609 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>G [Show Flanks]
        Chromosome:
        6:31622458 (GRCh38)
        6:31590235 (GRCh37)
        Canonical SPDI:
        NC_000006.12:31622457:A:G
        Gene:
        PRRC2A (Varview), SNORA38 (Varview)
        Functional Consequence:
        2KB_upstream_variant,upstream_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        G=0.000071/1 (ALFA)
        G=0.000004/1 (TOPMED)
        G=0.000007/1 (GnomAD)
        ...more
        HGVS:
        5.

        rs1486015138 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>A [Show Flanks]
          Chromosome:
          6:31623101 (GRCh38)
          6:31590878 (GRCh37)
          Canonical SPDI:
          NC_000006.12:31623100:T:A
          Gene:
          PRRC2A (Varview), SNORA38 (Varview)
          Functional Consequence:
          non_coding_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          A=0./0 (ALFA)
          A=0.000004/1 (TOPMED)
          A=0.000007/1 (GnomAD)
          ...more
          HGVS:
          6.
          7.

          rs1484480110 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>T [Show Flanks]
            Chromosome:
            6:31623424 (GRCh38)
            6:31591201 (GRCh37)
            Canonical SPDI:
            NC_000006.12:31623423:C:T
            Gene:
            PRRC2A (Varview), SNORA38 (Varview)
            Functional Consequence:
            downstream_transcript_variant,500B_downstream_variant,intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            T=0./0 (ALFA)
            T=0.000004/1 (TOPMED)
            HGVS:
            8.

            rs1484377144 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              G>T [Show Flanks]
              Chromosome:
              6:31622553 (GRCh38)
              6:31590330 (GRCh37)
              Canonical SPDI:
              NC_000006.12:31622552:G:T
              Gene:
              PRRC2A (Varview), SNORA38 (Varview)
              Functional Consequence:
              2KB_upstream_variant,upstream_transcript_variant,intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0./0 (ALFA)
              T=0.000004/1 (TOPMED)
              T=0.000007/1 (GnomAD)
              T=0.000071/1 (TOMMO)
              ...more
              HGVS:
              9.

              rs1483476484 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                6:31621883 (GRCh38)
                6:31589660 (GRCh37)
                Canonical SPDI:
                NC_000006.12:31621882:G:A
                Gene:
                PRRC2A (Varview), SNORA38 (Varview)
                Functional Consequence:
                2KB_upstream_variant,upstream_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                A=0./0 (ALFA)
                A=0.000007/1 (GnomAD)
                HGVS:
                10.

                rs1481889165 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  6:31622023 (GRCh38)
                  6:31589800 (GRCh37)
                  Canonical SPDI:
                  NC_000006.12:31622022:A:G
                  Gene:
                  PRRC2A (Varview), SNORA38 (Varview)
                  Functional Consequence:
                  2KB_upstream_variant,upstream_transcript_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000011/3 (TOPMED)
                  G=0.000014/2 (GnomAD)
                  ...more
                  HGVS:
                  11.

                  rs1480827399 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>T [Show Flanks]
                    Chromosome:
                    6:31621384 (GRCh38)
                    6:31589161 (GRCh37)
                    Canonical SPDI:
                    NC_000006.12:31621383:C:T
                    Gene:
                    PRRC2A (Varview), SNORA38 (Varview)
                    Functional Consequence:
                    2KB_upstream_variant,upstream_transcript_variant,intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    T=0.000142/2 (ALFA)
                    T=0.000014/2 (GnomAD)
                    T=0.000035/1 (TOMMO)
                    T=0.000038/10 (TOPMED)
                    ...more
                    HGVS:
                    12.

                    rs1478944921 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      6:31621247 (GRCh38)
                      6:31589024 (GRCh37)
                      Canonical SPDI:
                      NC_000006.12:31621246:G:A
                      Gene:
                      PRRC2A (Varview), SNORA38 (Varview)
                      Functional Consequence:
                      2KB_upstream_variant,upstream_transcript_variant,intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.00006/16 (TOPMED)
                      A=0.000086/12 (GnomAD)
                      ...more
                      HGVS:
                      13.

                      rs1476583070 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        6:31622190 (GRCh38)
                        6:31589967 (GRCh37)
                        Canonical SPDI:
                        NC_000006.12:31622189:C:T
                        Gene:
                        PRRC2A (Varview), SNORA38 (Varview)
                        Functional Consequence:
                        2KB_upstream_variant,upstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0.000071/1 (ALFA)
                        T=0.000004/1 (TOPMED)
                        T=0.000007/1 (GnomAD)
                        ...more
                        HGVS:
                        14.

                        rs1476070578 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>T [Show Flanks]
                          Chromosome:
                          6:31621244 (GRCh38)
                          6:31589021 (GRCh37)
                          Canonical SPDI:
                          NC_000006.12:31621243:G:T
                          Gene:
                          PRRC2A (Varview), SNORA38 (Varview)
                          Functional Consequence:
                          2KB_upstream_variant,upstream_transcript_variant,intron_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          T=0./0 (ALFA)
                          T=0.000011/3 (TOPMED)
                          HGVS:
                          15.

                          rs1475059161 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>C [Show Flanks]
                            Chromosome:
                            6:31622828 (GRCh38)
                            6:31590605 (GRCh37)
                            Canonical SPDI:
                            NC_000006.12:31622827:T:C
                            Gene:
                            PRRC2A (Varview), SNORA38 (Varview)
                            Functional Consequence:
                            2KB_upstream_variant,upstream_transcript_variant,synonymous_variant,coding_sequence_variant
                            Validated:
                            by frequency
                            MAF:
                            C=0.000004/1 (GnomAD_exomes)
                            HGVS:
                            18.

                            rs1474499219 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>G [Show Flanks]
                              Chromosome:
                              6:31622643 (GRCh38)
                              6:31590420 (GRCh37)
                              Canonical SPDI:
                              NC_000006.12:31622642:A:G
                              Gene:
                              PRRC2A (Varview), SNORA38 (Varview)
                              Functional Consequence:
                              2KB_upstream_variant,upstream_transcript_variant,intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0./0 (ALFA)
                              G=0.000007/1 (GnomAD)
                              G=0.000015/4 (TOPMED)
                              ...more
                              HGVS:
                              19.

                              rs1474025346 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>G [Show Flanks]
                                Chromosome:
                                6:31623516 (GRCh38)
                                6:31591293 (GRCh37)
                                Canonical SPDI:
                                NC_000006.12:31623515:C:G
                                Gene:
                                PRRC2A (Varview), SNORA38 (Varview)
                                Functional Consequence:
                                500B_downstream_variant,downstream_transcript_variant,intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000008/2 (TOPMED)
                                HGVS:
                                20.

                                rs1473586211 has merged into rs3993756 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  TTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                                  Chromosome:
                                  6:31623272 (GRCh38)
                                  6:31591049 (GRCh37)
                                  Canonical SPDI:
                                  NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:31623259:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                                  Gene:
                                  PRRC2A (Varview), SNORA38 (Varview)
                                  Functional Consequence:
                                  downstream_transcript_variant,500B_downstream_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  TTTTTTTTTTTT=0./0 (ALFA)
                                  -=0.3544/1775 (1000Genomes)
                                  HGVS:
                                  NC_000006.12:g.31623272_31623284del, NC_000006.12:g.31623273_31623284del, NC_000006.12:g.31623274_31623284del, NC_000006.12:g.31623275_31623284del, NC_000006.12:g.31623276_31623284del, NC_000006.12:g.31623277_31623284del, NC_000006.12:g.31623278_31623284del, NC_000006.12:g.31623279_31623284del, NC_000006.12:g.31623280_31623284del, NC_000006.12:g.31623281_31623284del, NC_000006.12:g.31623282_31623284del, NC_000006.12:g.31623283_31623284del, NC_000006.12:g.31623284del, NC_000006.12:g.31623284dup, NC_000006.12:g.31623283_31623284dup, NC_000006.12:g.31623282_31623284dup, NC_000006.12:g.31623281_31623284dup, NC_000006.12:g.31623280_31623284dup, NC_000006.12:g.31623279_31623284dup, NC_000006.12:g.31623278_31623284dup, NC_000006.12:g.31623277_31623284dup, NC_000006.12:g.31623276_31623284dup, NC_000006.12:g.31623275_31623284dup, NC_000006.12:g.31623272_31623284dup, NC_000006.12:g.31623271_31623284dup, NC_000006.12:g.31623261_31623284dup, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.31623284_31623285insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591049_31591061del, NC_000006.11:g.31591050_31591061del, NC_000006.11:g.31591051_31591061del, NC_000006.11:g.31591052_31591061del, NC_000006.11:g.31591053_31591061del, NC_000006.11:g.31591054_31591061del, NC_000006.11:g.31591055_31591061del, NC_000006.11:g.31591056_31591061del, NC_000006.11:g.31591057_31591061del, NC_000006.11:g.31591058_31591061del, NC_000006.11:g.31591059_31591061del, NC_000006.11:g.31591060_31591061del, NC_000006.11:g.31591061del, NC_000006.11:g.31591061dup, NC_000006.11:g.31591060_31591061dup, NC_000006.11:g.31591059_31591061dup, NC_000006.11:g.31591058_31591061dup, NC_000006.11:g.31591057_31591061dup, NC_000006.11:g.31591056_31591061dup, NC_000006.11:g.31591055_31591061dup, NC_000006.11:g.31591054_31591061dup, NC_000006.11:g.31591053_31591061dup, NC_000006.11:g.31591052_31591061dup, NC_000006.11:g.31591049_31591061dup, NC_000006.11:g.31591048_31591061dup, NC_000006.11:g.31591038_31591061dup, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.31591061_31591062insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100558_3100570del, NT_113891.3:g.3100559_3100570del, NT_113891.3:g.3100560_3100570del, NT_113891.3:g.3100561_3100570del, NT_113891.3:g.3100562_3100570del, NT_113891.3:g.3100563_3100570del, NT_113891.3:g.3100564_3100570del, NT_113891.3:g.3100565_3100570del, NT_113891.3:g.3100566_3100570del, NT_113891.3:g.3100567_3100570del, NT_113891.3:g.3100568_3100570del, NT_113891.3:g.3100569_3100570del, NT_113891.3:g.3100570del, NT_113891.3:g.3100570dup, NT_113891.3:g.3100569_3100570dup, NT_113891.3:g.3100568_3100570dup, NT_113891.3:g.3100567_3100570dup, NT_113891.3:g.3100566_3100570dup, NT_113891.3:g.3100565_3100570dup, NT_113891.3:g.3100564_3100570dup, NT_113891.3:g.3100563_3100570dup, NT_113891.3:g.3100562_3100570dup, NT_113891.3:g.3100561_3100570dup, NT_113891.3:g.3100558_3100570dup, NT_113891.3:g.3100557_3100570dup, NT_113891.3:g.3100547_3100570dup, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3100570_3100571insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100664_3100676del, NT_113891.2:g.3100665_3100676del, NT_113891.2:g.3100666_3100676del, NT_113891.2:g.3100667_3100676del, NT_113891.2:g.3100668_3100676del, NT_113891.2:g.3100669_3100676del, NT_113891.2:g.3100670_3100676del, NT_113891.2:g.3100671_3100676del, NT_113891.2:g.3100672_3100676del, NT_113891.2:g.3100673_3100676del, NT_113891.2:g.3100674_3100676del, NT_113891.2:g.3100675_3100676del, NT_113891.2:g.3100676del, NT_113891.2:g.3100676dup, NT_113891.2:g.3100675_3100676dup, NT_113891.2:g.3100674_3100676dup, NT_113891.2:g.3100673_3100676dup, NT_113891.2:g.3100672_3100676dup, NT_113891.2:g.3100671_3100676dup, NT_113891.2:g.3100670_3100676dup, NT_113891.2:g.3100669_3100676dup, NT_113891.2:g.3100668_3100676dup, NT_113891.2:g.3100667_3100676dup, NT_113891.2:g.3100664_3100676dup, NT_113891.2:g.3100663_3100676dup, NT_113891.2:g.3100653_3100676dup, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3100676_3100677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879092_2879104del, NT_167248.2:g.2879093_2879104del, NT_167248.2:g.2879094_2879104del, NT_167248.2:g.2879095_2879104del, NT_167248.2:g.2879096_2879104del, NT_167248.2:g.2879097_2879104del, NT_167248.2:g.2879098_2879104del, NT_167248.2:g.2879099_2879104del, NT_167248.2:g.2879100_2879104del, NT_167248.2:g.2879101_2879104del, NT_167248.2:g.2879102_2879104del, NT_167248.2:g.2879103_2879104del, NT_167248.2:g.2879104del, NT_167248.2:g.2879104dup, NT_167248.2:g.2879103_2879104dup, NT_167248.2:g.2879102_2879104dup, NT_167248.2:g.2879101_2879104dup, NT_167248.2:g.2879100_2879104dup, NT_167248.2:g.2879099_2879104dup, NT_167248.2:g.2879098_2879104dup, NT_167248.2:g.2879097_2879104dup, NT_167248.2:g.2879096_2879104dup, NT_167248.2:g.2879095_2879104dup, NT_167248.2:g.2879092_2879104dup, NT_167248.2:g.2879091_2879104dup, NT_167248.2:g.2879081_2879104dup, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.2879104_2879105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884688_2884700del, NT_167248.1:g.2884689_2884700del, NT_167248.1:g.2884690_2884700del, NT_167248.1:g.2884691_2884700del, NT_167248.1:g.2884692_2884700del, NT_167248.1:g.2884693_2884700del, NT_167248.1:g.2884694_2884700del, NT_167248.1:g.2884695_2884700del, NT_167248.1:g.2884696_2884700del, NT_167248.1:g.2884697_2884700del, NT_167248.1:g.2884698_2884700del, NT_167248.1:g.2884699_2884700del, NT_167248.1:g.2884700del, NT_167248.1:g.2884700dup, NT_167248.1:g.2884699_2884700dup, NT_167248.1:g.2884698_2884700dup, NT_167248.1:g.2884697_2884700dup, NT_167248.1:g.2884696_2884700dup, NT_167248.1:g.2884695_2884700dup, NT_167248.1:g.2884694_2884700dup, NT_167248.1:g.2884693_2884700dup, NT_167248.1:g.2884692_2884700dup, NT_167248.1:g.2884691_2884700dup, NT_167248.1:g.2884688_2884700dup, NT_167248.1:g.2884687_2884700dup, NT_167248.1:g.2884677_2884700dup, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.2884700_2884701insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871046_2871048dup, NT_167245.2:g.2871039_2871048del, NT_167245.2:g.2871040_2871048del, NT_167245.2:g.2871041_2871048del, NT_167245.2:g.2871042_2871048del, NT_167245.2:g.2871043_2871048del, NT_167245.2:g.2871044_2871048del, NT_167245.2:g.2871045_2871048del, NT_167245.2:g.2871046_2871048del, NT_167245.2:g.2871047_2871048del, NT_167245.2:g.2871048del, NT_167245.2:g.2871048dup, NT_167245.2:g.2871047_2871048dup, NT_167245.2:g.2871045_2871048dup, NT_167245.2:g.2871044_2871048dup, NT_167245.2:g.2871043_2871048dup, NT_167245.2:g.2871042_2871048dup, NT_167245.2:g.2871041_2871048dup, NT_167245.2:g.2871040_2871048dup, NT_167245.2:g.2871039_2871048dup, NT_167245.2:g.2871038_2871048dup, NT_167245.2:g.2871037_2871048dup, NT_167245.2:g.2871036_2871048dup, NT_167245.2:g.2871033_2871048dup, NT_167245.2:g.2871032_2871048dup, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.2:g.2871048_2871049insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922552_2922564del, NT_167249.2:g.2922553_2922564del, NT_167249.2:g.2922554_2922564del, NT_167249.2:g.2922555_2922564del, NT_167249.2:g.2922556_2922564del, NT_167249.2:g.2922557_2922564del, NT_167249.2:g.2922558_2922564del, NT_167249.2:g.2922559_2922564del, NT_167249.2:g.2922560_2922564del, NT_167249.2:g.2922561_2922564del, NT_167249.2:g.2922562_2922564del, NT_167249.2:g.2922563_2922564del, NT_167249.2:g.2922564del, NT_167249.2:g.2922564dup, NT_167249.2:g.2922563_2922564dup, NT_167249.2:g.2922562_2922564dup, NT_167249.2:g.2922561_2922564dup, NT_167249.2:g.2922560_2922564dup, NT_167249.2:g.2922559_2922564dup, NT_167249.2:g.2922558_2922564dup, NT_167249.2:g.2922557_2922564dup, NT_167249.2:g.2922556_2922564dup, NT_167249.2:g.2922555_2922564dup, NT_167249.2:g.2922552_2922564dup, NT_167249.2:g.2922551_2922564dup, NT_167249.2:g.2922541_2922564dup, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.2922564_2922565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921850_2921862del, NT_167249.1:g.2921851_2921862del, NT_167249.1:g.2921852_2921862del, NT_167249.1:g.2921853_2921862del, NT_167249.1:g.2921854_2921862del, NT_167249.1:g.2921855_2921862del, NT_167249.1:g.2921856_2921862del, NT_167249.1:g.2921857_2921862del, NT_167249.1:g.2921858_2921862del, NT_167249.1:g.2921859_2921862del, NT_167249.1:g.2921860_2921862del, NT_167249.1:g.2921861_2921862del, NT_167249.1:g.2921862del, NT_167249.1:g.2921862dup, NT_167249.1:g.2921861_2921862dup, NT_167249.1:g.2921860_2921862dup, NT_167249.1:g.2921859_2921862dup, NT_167249.1:g.2921858_2921862dup, NT_167249.1:g.2921857_2921862dup, NT_167249.1:g.2921856_2921862dup, NT_167249.1:g.2921855_2921862dup, NT_167249.1:g.2921854_2921862dup, NT_167249.1:g.2921853_2921862dup, NT_167249.1:g.2921850_2921862dup, NT_167249.1:g.2921849_2921862dup, NT_167249.1:g.2921839_2921862dup, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.2921862_2921863insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.2928313_2928325del, NT_167246.2:g.2928314_2928325del, NT_167246.2:g.2928315_2928325del, NT_167246.2:g.2928316_2928325del, NT_167246.2:g.2928317_2928325del, NT_167246.2:g.2928318_2928325del, NT_167246.2:g.2928319_2928325del, NT_167246.2:g.2928320_2928325del, NT_167246.2:g.2928321_2928325del, NT_167246.2:g.2928322_2928325del, NT_167246.2:g.2928323_2928325del, NT_167246.2:g.2928324_2928325del, NT_167246.2:g.2928325del, NT_167246.2:g.2928325dup, NT_167246.2:g.2928324_2928325dup, NT_167246.2:g.2928323_2928325dup, NT_167246.2:g.2928322_2928325dup, NT_167246.2:g.2928321_2928325dup, NT_167246.2:g.2928320_2928325dup, NT_167246.2:g.2928319_2928325dup, NT_167246.2:g.2928318_2928325dup, NT_167246.2:g.2928317_2928325dup, NT_167246.2:g.2928316_2928325dup, NT_167246.2:g.2928313_2928325dup, NT_167246.2:g.2928312_2928325dup, NT_167246.2:g.2928302_2928325dup, NT_167246.2:g.2928299_2928325dup, NT_167246.2:g.2928298_2928325dup, NT_167246.2:g.2928325_2928326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.2928325_2928326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.2928325_2928326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.2928325_2928326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.2928325_2928326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.2928325_2928326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.2928325_2928326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.2928325_2928326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.2928325_2928326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.2933933_2933945del, NT_167246.1:g.2933934_2933945del, NT_167246.1:g.2933935_2933945del, NT_167246.1:g.2933936_2933945del, NT_167246.1:g.2933937_2933945del, NT_167246.1:g.2933938_2933945del, NT_167246.1:g.2933939_2933945del, NT_167246.1:g.2933940_2933945del, NT_167246.1:g.2933941_2933945del, NT_167246.1:g.2933942_2933945del, NT_167246.1:g.2933943_2933945del, NT_167246.1:g.2933944_2933945del, NT_167246.1:g.2933945del, NT_167246.1:g.2933945dup, NT_167246.1:g.2933944_2933945dup, NT_167246.1:g.2933943_2933945dup, NT_167246.1:g.2933942_2933945dup, NT_167246.1:g.2933941_2933945dup, NT_167246.1:g.2933940_2933945dup, NT_167246.1:g.2933939_2933945dup, NT_167246.1:g.2933938_2933945dup, NT_167246.1:g.2933937_2933945dup, NT_167246.1:g.2933936_2933945dup, NT_167246.1:g.2933933_2933945dup, NT_167246.1:g.2933932_2933945dup, NT_167246.1:g.2933922_2933945dup, NT_167246.1:g.2933919_2933945dup, NT_167246.1:g.2933918_2933945dup, NT_167246.1:g.2933945_2933946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.2933945_2933946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.2933945_2933946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.2933945_2933946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.2933945_2933946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.2933945_2933946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.2933945_2933946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.2933945_2933946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.2933945_2933946insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965160_2965164dup, NT_167247.2:g.2965157_2965164del, NT_167247.2:g.2965158_2965164del, NT_167247.2:g.2965159_2965164del, NT_167247.2:g.2965160_2965164del, NT_167247.2:g.2965161_2965164del, NT_167247.2:g.2965162_2965164del, NT_167247.2:g.2965163_2965164del, NT_167247.2:g.2965164del, NT_167247.2:g.2965164dup, NT_167247.2:g.2965163_2965164dup, NT_167247.2:g.2965162_2965164dup, NT_167247.2:g.2965161_2965164dup, NT_167247.2:g.2965159_2965164dup, NT_167247.2:g.2965158_2965164dup, NT_167247.2:g.2965157_2965164dup, NT_167247.2:g.2965156_2965164dup, NT_167247.2:g.2965155_2965164dup, NT_167247.2:g.2965154_2965164dup, NT_167247.2:g.2965153_2965164dup, NT_167247.2:g.2965152_2965164dup, NT_167247.2:g.2965151_2965164dup, NT_167247.2:g.2965150_2965164dup, NT_167247.2:g.2965147_2965164dup, NT_167247.2:g.2965146_2965164dup, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.2:g.2965164_2965165insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876631_2876633dup, NT_167245.1:g.2876624_2876633del, NT_167245.1:g.2876625_2876633del, NT_167245.1:g.2876626_2876633del, NT_167245.1:g.2876627_2876633del, NT_167245.1:g.2876628_2876633del, NT_167245.1:g.2876629_2876633del, NT_167245.1:g.2876630_2876633del, NT_167245.1:g.2876631_2876633del, NT_167245.1:g.2876632_2876633del, NT_167245.1:g.2876633del, NT_167245.1:g.2876633dup, NT_167245.1:g.2876632_2876633dup, NT_167245.1:g.2876630_2876633dup, NT_167245.1:g.2876629_2876633dup, NT_167245.1:g.2876628_2876633dup, NT_167245.1:g.2876627_2876633dup, NT_167245.1:g.2876626_2876633dup, NT_167245.1:g.2876625_2876633dup, NT_167245.1:g.2876624_2876633dup, NT_167245.1:g.2876623_2876633dup, NT_167245.1:g.2876622_2876633dup, NT_167245.1:g.2876621_2876633dup, NT_167245.1:g.2876618_2876633dup, NT_167245.1:g.2876617_2876633dup, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167245.1:g.2876633_2876634insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970745_2970749dup, NT_167247.1:g.2970742_2970749del, NT_167247.1:g.2970743_2970749del, NT_167247.1:g.2970744_2970749del, NT_167247.1:g.2970745_2970749del, NT_167247.1:g.2970746_2970749del, NT_167247.1:g.2970747_2970749del, NT_167247.1:g.2970748_2970749del, NT_167247.1:g.2970749del, NT_167247.1:g.2970749dup, NT_167247.1:g.2970748_2970749dup, NT_167247.1:g.2970747_2970749dup, NT_167247.1:g.2970746_2970749dup, NT_167247.1:g.2970744_2970749dup, NT_167247.1:g.2970743_2970749dup, NT_167247.1:g.2970742_2970749dup, NT_167247.1:g.2970741_2970749dup, NT_167247.1:g.2970740_2970749dup, NT_167247.1:g.2970739_2970749dup, NT_167247.1:g.2970738_2970749dup, NT_167247.1:g.2970737_2970749dup, NT_167247.1:g.2970736_2970749dup, NT_167247.1:g.2970735_2970749dup, NT_167247.1:g.2970732_2970749dup, NT_167247.1:g.2970731_2970749dup, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167247.1:g.2970749_2970750insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                                  ...more

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