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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
    nsv7048812inversion1nstd229human GRCh38 chr7: 732,942-1,080,874 , GRCh37.p13 chr7: 772,579-1,120,510 GPR146, LOC105375120, 8 more genes
    nsv7045642inversion1nstd229human GRCh38 chr7: 1,011,666-1,336,840 , GRCh37.p13 chr7: 1,051,302-1,376,476 MIR339, ZFAND2A-DT, 7 more genes
    nsv6811077copy number variation1nstd229human GRCh38 chr7: 1,050,165-1,075,620 , GRCh37.p13 chr7: 1,089,801-1,115,256 GPR146, LOC105375120, 1 more genes
    nsv6811068copy number variation1nstd229human GRCh38 chr7: 990,725-1,080,383 , GRCh37.p13 chr7: 1,030,361-1,120,019 LOC105375120, C7orf50, 2 more genes
    nsv6807577copy number variation1nstd229human GRCh38 chr7: 1,059,592-1,068,289 , GRCh37.p13 chr7: 1,099,228-1,107,925 C7orf50, GPR146
    nsv6807401copy number variation1nstd229human GRCh38 chr7: 1,014,501-1,116,500 , GRCh37.p13 chr7: 1,054,137-1,156,136 GPER1, GPR146, 3 more genes
    nsv6800581copy number variation1nstd229human GRCh38 chr7: 1,044,463-1,044,507 , GRCh37.p13 chr7: 1,084,099-1,084,143 C7orf50, GPR146
    nsv6799215copy number variation1nstd229human GRCh38 chr7: 1,006,505-1,057,391 , GRCh37.p13 chr7: 1,046,141-1,097,027 GPR146, C7orf50, 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
    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
    nsv6604253copy number variation1nstd223human GRCh38 chr7: 1,050,345-1,052,876 , GRCh37.p13 chr7: 1,089,981-1,092,512 GPR146, C7orf50
    nsv6602015copy number variation1nstd223human GRCh38 chr7: 1,044,301-1,044,800 , GRCh37.p13 chr7: 1,083,937-1,084,436 GPR146, C7orf50
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6290909copy number variation1nstd102humanUncertain significance GRCh37 chr7: 989,697-2,138,529 , GRCh38.p12 chr7: 950,061-2,098,894 PSMG3, TFAMP1, 29 more genes
    nsv6261004mobile element insertion1nstd215human GRCh38 chr7: 1,044,014-1,044,014 , GRCh37.p13 chr7: 1,083,650-1,083,650 C7orf50, GPR146
    nsv6175803copy number variation1nstd214human GRCh38 chr7: 1,044,314-1,044,387 , GRCh37.p13 chr7: 1,083,950-1,084,023 GPR146, C7orf50
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