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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7148154copy number variation1nstd102humanPathogenic GRCh38 chr7: 154,446,117-159,206,757 , GRCh37.p13 chr7: 154,143,202-158,999,446 LOC105375602, LOC105375599, 70 more genes
    nsv7097356copy number variation2nstd102humanPathogenic GRCh37 chr7: 152,617,597-158,500,659 , GRCh38.p12 chr7: 152,920,512-158,707,968 LOC107986722, LOC105375593, 76 more genes
    nsv7075177inversion1nstd229human GRCh38 chr7: 156,968,222-156,975,321 , GRCh37.p13 chr7: 156,760,916-156,768,015 NOM1
    nsv7066235inversion1nstd229human GRCh38 chr7: 156,970,745-156,975,106 , GRCh37.p13 chr7: 156,763,439-156,767,800 NOM1
    nsv6836085copy number variation1nstd229human GRCh38 chr7: 156,819,301-157,193,100 , GRCh37.p13 chr7: 156,611,995-156,985,794 UBE3C, LOC645272, 12 more genes
    nsv6835763copy number variation1nstd229human GRCh38 chr7: 156,936,301-156,949,700 , GRCh37.p13 chr7: 156,728,995-156,742,394 LOC105375604, LOC105375605, 1 more genes
    nsv6828148copy number variation1nstd229human GRCh38 chr7: 156,958,100-156,966,311 , GRCh37.p13 chr7: 156,750,794-156,759,005 NOM1
    nsv6826540copy number variation1nstd229human GRCh38 chr7: 156,941,548-156,950,148 , GRCh37.p13 chr7: 156,734,242-156,742,842 LOC105375605, NOM1
    nsv6824309copy number variation1nstd229human GRCh38 chr7: 156,964,392-156,967,899 , GRCh37.p13 chr7: 156,757,086-156,760,593 NOM1
    nsv6823564copy number variation1nstd229human GRCh38 chr7: 156,957,885-156,959,338 , GRCh37.p13 chr7: 156,750,579-156,752,032 NOM1
    nsv6822045copy number variation1nstd229human GRCh38 chr7: 156,942,552-156,948,303 , GRCh37.p13 chr7: 156,735,246-156,740,997 LOC105375605, NOM1
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6571756inversion1nstd223human GRCh38 chr7: 156,973,444-156,974,431 , GRCh37.p13 chr7: 156,766,138-156,767,125 NOM1
    nsv6561986inversion1nstd223human GRCh38 chr7: 156,973,426-156,974,383 , GRCh37.p13 chr7: 156,766,120-156,767,077 NOM1
    nsv6429432copy number variation1nstd223human GRCh38 chr7: 156,958,050-156,959,337 , GRCh37.p13 chr7: 156,750,744-156,752,031 NOM1
    nsv6425721copy number variation1nstd223human GRCh38 chr7: 156,968,221-156,970,790 , GRCh37.p13 chr7: 156,760,915-156,763,484 NOM1
    nsv6425513copy number variation1nstd223human GRCh38 chr7: 156,951,379-156,957,605 , GRCh37.p13 chr7: 156,744,073-156,750,299 NOM1
    nsv6315450copy number variation1nstd102humanPathogenic GRCh37 chr7: 155,389,460-157,960,969 , GRCh38.p12 chr7: 155,596,766-158,168,277 RNF32, MIR153-2, 38 more genes
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