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Items: 1 to 20 of 296

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097362copy number variation1nstd102humanPathogenic GRCh37 chr7: 193,200-1,498,962 , GRCh38.p12 chr7: 193,200-1,459,326 ZFAND2A-DT, MICALL2, 28 more genes
    nsv7050264inversion1nstd229human GRCh38 chr7: 1,220,977-1,240,812 , GRCh37.p13 chr7: 1,260,613-1,280,448 UNCX
    nsv7045642inversion1nstd229human GRCh38 chr7: 1,011,666-1,336,840 , GRCh37.p13 chr7: 1,051,302-1,376,476 MIR339, ZFAND2A-DT, 7 more genes
    nsv7044854inversion1nstd229human GRCh38 chr7: 1,222,704-1,284,876 , GRCh37.p13 chr7: 1,262,340-1,324,512 UNCX
    nsv6812599copy number variation1nstd229human GRCh38 chr7: 1,110,364-1,254,582 , GRCh37.p13 chr7: 1,150,000-1,294,218 ZFAND2A-DT, C7orf50, 3 more genes
    nsv6808237copy number variation1nstd229human GRCh38 chr7: 1,233,001-1,235,800 , GRCh37.p13 chr7: 1,272,637-1,275,436 UNCX
    nsv6807370copy number variation1nstd229human GRCh38 chr7: 1,195,801-1,455,600 , GRCh37.p13 chr7: 1,235,437-1,495,236 UNCX, MICALL2
    nsv6805668copy number variation1nstd229human GRCh38 chr7: 1,156,501-1,290,700 , GRCh37.p13 chr7: 1,196,137-1,330,336 ZFAND2A-DT, ZFAND2A, 1 more genes
    nsv6798922copy number variation1nstd229human GRCh38 chr7: 680,698-1,325,106 , GRCh37.p13 chr7: 720,335-1,364,742 DNAAF5, MIR339, 14 more genes
    nsv6798214copy number variation1nstd229human GRCh38 chr7: 1,231,107-1,231,541 , GRCh37.p13 chr7: 1,270,743-1,271,177 UNCX
    nsv6636783copy number variation1nstd102humanUncertain significance GRCh37 chr7: 1,142,498-1,376,883 , GRCh38.p12 chr7: 1,102,862-1,337,247 UNCX, LOC102723758, 3 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634339copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-9,649,794 , GRCh38.p12 chr7: 43,360-9,610,164 MRM2, FOXL3, 182 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632476copy number variation1nstd224human GRCh37 chr7: 93,811-2,255,893 , GRCh38.p12 chr7: 93,811-2,216,258 INTS1, DNAAF5, 52 more genes
    nsv6631557copy number variation1nstd224human GRCh37 chr7: 1,260,636-1,377,077 , GRCh38.p12 chr7: 1,221,000-1,337,441 UNCX
    nsv6611795copy number variation1nstd223human GRCh38 chr7: 1,236,947-1,377,161 , GRCh37.p13 chr7: 1,276,583-1,416,797 UNCX
    nsv6609691copy number variation1nstd223human GRCh38 chr7: 1,232,201-1,233,500 , GRCh37.p13 chr7: 1,271,837-1,273,136 UNCX
    nsv6607797copy number variation1nstd223human GRCh38 chr7: 1,196,409-1,341,939 , GRCh37.p13 chr7: 1,236,045-1,381,575 UNCX
    nsv6605857copy number variation1nstd223human GRCh38 chr7: 1,235,101-1,239,200 , GRCh37.p13 chr7: 1,274,737-1,278,836 UNCX
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