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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7039284inversion1nstd229human GRCh38 chr3: 15,253,174-15,254,104 , GRCh37.p13 chr3: 15,294,681-15,295,611 SH3BP5, SH3BP5-AS1, 1 more genes
    nsv6717887copy number variation1nstd229human GRCh38 chr3: 15,206,001-15,207,200 , GRCh37.p13 chr3: 15,247,508-15,248,707 CAPN7, COL6A4P1
    nsv6714327copy number variation1nstd229human GRCh38 chr3: 15,244,536-15,246,182 , GRCh37.p13 chr3: 15,286,043-15,287,689 CAPN7
    nsv6712034copy number variation1nstd229human GRCh38 chr3: 14,670,901-15,564,100 , GRCh37.p13 chr3: 14,712,408-15,605,607 COLQ, RNU6-1024P, 22 more genes
    nsv6705548copy number variation1nstd229human GRCh38 chr3: 15,200,801-15,220,100 , GRCh37.p13 chr3: 15,242,308-15,261,607 CAPN7, COL6A4P1
    nsv6703151copy number variation1nstd229human GRCh38 chr3: 15,198,701-15,242,700 , GRCh37.p13 chr3: 15,240,208-15,284,207 COL6A4P1, CAPN7
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6547393inversion1nstd223human GRCh38 chr3: 15,221,185-15,221,966 , GRCh37.p13 chr3: 15,262,692-15,263,473 CAPN7
    nsv6367270copy number variation1nstd223human GRCh38 chr3: 15,244,501-15,245,500 , GRCh37.p13 chr3: 15,286,008-15,287,007 CAPN7
    nsv6359383copy number variation1nstd223human GRCh38 chr3: 15,110,376-15,205,291 , GRCh37.p13 chr3: 15,151,883-15,246,798 COL6A4P1, CAPN7, 2 more genes
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    nsv6291013copy number variation1nstd102humanUncertain significance GRCh37 chr3: 15,085,863-16,402,392 , GRCh38.p12 chr3: 15,044,356-16,360,885 MIR563, RNU6-1024P, 30 more genes
    nsv6253728mobile element insertion1nstd215human GRCh37.p13 chr3: 15,294,342-15,294,342 , GRCh38 chr3: 15,252,835-15,252,835 SH3BP5, CAPN7, 1 more genes
    nsv6043273insertion1nstd212human GRCh38 chr3: 15,224,240-15,224,240 , GRCh37.p13 chr3: 15,265,747-15,265,747 CAPN7
    nsv5968065inversion1nstd209human GRCh38 chr3: 14,742,874-15,551,121 , GRCh37.p13 chr3: 14,784,381-15,592,628 , NR2C2, 21 more genes
    nsv5965635insertion1nstd209human GRCh37.p13 chr3: 15,294,326-15,294,326 , GRCh38 chr3: 15,252,819-15,252,819 SH3BP5, CAPN7, 1 more genes
    nsv5692553mobile element insertion2nstd211human GRCh38 chr3: 15,238,873-15,238,873 , GRCh37.p13 chr3: 15,280,380-15,280,380 CAPN7
    nsv5679861mobile element insertion2nstd211human GRCh38 chr3: 15,252,835-15,252,835 , GRCh37.p13 chr3: 15,294,342-15,294,342 SH3BP5, CAPN7, 1 more genes
    nsv5606581insertion1nstd207human GRCh38 chr3: 15,252,826-15,252,826 , GRCh37.p13 chr3: 15,294,333-15,294,333 SH3BP5, CAPN7, 1 more genes
    nsv5559332sequence alteration1nstd206human GRCh38 chr3: 15,253,173-15,254,103 , GRCh37.p13 chr3: 15,294,680-15,295,610 SH3BP5, CAPN7, 1 more genes
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