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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147120copy number variation1nstd232human GRCh37.p13 chr7: 2,406,083-2,406,158 , GRCh38.p12 chr7: 2,366,448-2,366,523 EIF3B
    nsv7144443insertion1nstd232human GRCh37.p13 chr7: 2,406,226-2,406,226 , GRCh38.p12 chr7: 2,366,591-2,366,591 EIF3B
    nsv7144255insertion1nstd232human GRCh37.p13 chr7: 2,403,395-2,403,395 , GRCh38.p12 chr7: 2,363,760-2,363,760 EIF3B
    nsv7141484copy number variation1nstd232human GRCh37.p13 chr7: 2,418,078-2,418,141 , GRCh38.p12 chr7: 2,378,443-2,378,506 EIF3B
    nsv7141277insertion1nstd232human GRCh37.p13 chr7: 2,404,167-2,404,167 , GRCh38.p12 chr7: 2,364,532-2,364,532 EIF3B
    nsv7138567insertion1nstd232human GRCh37.p13 chr7: 2,395,054-2,395,054 , GRCh38.p12 chr7: 2,355,419-2,355,419 EIF3B
    nsv7138244insertion1nstd232human GRCh37.p13 chr7: 2,417,765-2,417,765 , GRCh38.p12 chr7: 2,378,130-2,378,130 EIF3B
    nsv7057091inversion1nstd229human GRCh38 chr7: 2,273,784-2,696,327 , GRCh37.p13 chr7: 2,313,419-2,735,961 BRAT1, NGRNP3, 13 more genes
    nsv7053928inversion1nstd229human GRCh38 chr7: 1,791,275-2,573,914 , GRCh37.p13 chr7: 1,830,911-2,613,548 MIR4655, LOC105375127, 19 more genes
    nsv7050776inversion1nstd229human GRCh38 chr7: 1,736,445-2,580,576 , GRCh37.p13 chr7: 1,776,081-2,620,210 IMMP1LP3, GRIFIN, 21 more genes
    nsv7042414inversion1nstd229human GRCh38 chr7: 2,257,030-2,573,543 , GRCh37.p13 chr7: 2,296,665-2,613,177 LOC107986759, GRIFIN, 11 more genes
    nsv7041506inversion1nstd229human GRCh38 chr7: 1,807,124-2,573,544 , GRCh37.p13 chr7: 1,846,760-2,613,178 CHST12, LOC100127955, 19 more genes
    nsv7041342inversion1nstd229human GRCh38 chr7: 2,373,099-2,382,344 , GRCh37.p13 chr7: 2,412,734-2,421,979 EIF3B, KIF19BP
    nsv6815704copy number variation1nstd229human GRCh38 chr7: 2,256,868-2,660,330 , GRCh37.p13 chr7: 2,296,503-2,699,964 NGRNP3, IMMP1LP3, 13 more genes
    nsv6814155copy number variation1nstd229human GRCh38 chr7: 2,342,375-2,364,022 , GRCh37.p13 chr7: 2,382,010-2,403,657 EIF3B, SNX8
    nsv6813126copy number variation1nstd229human GRCh38 chr7: 2,368,399-2,368,956 , GRCh37.p13 chr7: 2,408,034-2,408,591 EIF3B
    nsv6811734copy number variation1nstd229human GRCh38 chr7: 2,099,185-2,523,523 , GRCh37.p13 chr7: 2,138,820-2,563,157 CHST12, NUDT1, 13 more genes
    nsv6808763copy number variation1nstd229human GRCh38 chr7: 2,361,837-2,647,130 , GRCh37.p13 chr7: 2,401,472-2,686,764 KIF19BP, TTYH3, 10 more genes
    nsv6804638copy number variation1nstd229human GRCh38 chr7: 2,359,001-2,521,600 , GRCh37.p13 chr7: 2,398,636-2,561,234 NGRNP3, GRIFIN, 5 more genes
    nsv6803024copy number variation1nstd229human GRCh38 chr7: 2,160,119-2,450,631 , GRCh37.p13 chr7: 2,199,754-2,490,266 MIR6836, SNX8, 9 more genes
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