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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148080copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,335,152-113,127,204 , GRCh38.p12 chr2: 110,577,575-112,369,627 MIR4771-2, BUB1, 33 more genes
    nsv7148068copy number variation1nstd102humanUncertain significance GRCh37 chr2: 111,395,541-113,090,065 , GRCh38.p12 chr2: 110,637,964-112,332,488 NDUFB4P6, SLC30A6P1, 28 more genes
    nsv7098850copy number variation1nstd102humanUncertain significance GRCh37 chr2: 111,368,292-113,191,030 , GRCh38.p12 chr2: 110,610,715-112,433,453 MERTK, MIR4435-2HG, 33 more genes
    nsv7051911inversion1nstd229human GRCh38 chr2: 111,199,183-111,199,303 , GRCh37.p13 chr2: 111,956,760-111,956,880 MIR4435-2HG
    nsv6694699copy number variation1nstd229human GRCh38 chr2: 111,481,478-111,481,522 , GRCh37.p13 chr2: 112,239,055-112,239,099 MIR4435-2HG
    nsv6692991copy number variation1nstd229human GRCh38 chr2: 111,472,003-111,478,694 , GRCh37.p13 chr2: 112,229,580-112,236,271 MIR4435-2HG
    nsv6690241copy number variation1nstd229human GRCh38 chr2: 111,242,946-111,252,809 , GRCh37.p13 chr2: 112,000,523-112,010,386 MIR4435-2HG
    nsv6682859copy number variation1nstd229human GRCh38 chr2: 111,242,201-111,251,000 , GRCh37.p13 chr2: 111,999,778-112,008,577 MIR4435-2HG
    nsv6681016copy number variation1nstd229human GRCh38 chr2: 111,238,059-111,238,172 , GRCh37.p13 chr2: 111,995,636-111,995,749 MIR4435-2HG
    nsv6637066copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 111,397,786-113,111,856 , GRCh38.p12 chr2: 110,640,209-112,354,279 BUB1, BCL2L11, 29 more genes
    nsv6636824copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,366,256-113,127,751 , GRCh38.p12 chr2: 110,608,679-112,370,174 PAFAH1B1P2, BUB1, 33 more genes
    nsv6636588copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 111,365,996-113,111,856 , GRCh38.p12 chr2: 110,608,419-112,354,279 BUB1, BCL2L11, 32 more genes
    nsv6636225copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,369,264-113,142,794 , GRCh38.p12 chr2: 110,611,687-112,385,217 RPL34P8, SNORD132, 32 more genes
    nsv6627673copy number variation1nstd224human GRCh37 chr2: 112,220,359-112,464,359 , GRCh38.p12 chr2: 111,462,782-111,706,782 MIR4435-2HG, RPL34P8, 4 more genes
    nsv6627672copy number variation1nstd224human GRCh37 chr2: 111,395,603-113,217,630 , GRCh38.p12 chr2: 110,638,026-112,460,053 ACOXL, TMEM87B, 30 more genes
    nsv6627671copy number variation2nstd224human GRCh37 chr2: 111,395,603-113,093,928 , GRCh38.p12 chr2: 110,638,026-112,336,351 BUB1, PAFAH1B1P2, 28 more genes
    nsv6627497copy number variation2nstd224human GRCh37 chr2: 111,399,346-113,103,748 , GRCh38.p12 chr2: 110,641,769-112,346,171 BUB1, MERTK, 29 more genes
    nsv6544104inversion1nstd223human GRCh38 chr2: 111,241,681-111,242,206 , GRCh37.p13 chr2: 111,999,258-111,999,783 MIR4435-2HG
    nsv6351766copy number variation1nstd223human GRCh38 chr2: 111,276,001-111,279,400 , GRCh37.p13 chr2: 112,033,578-112,036,977 LOC101927283, MIR4435-2HG
    nsv6351399copy number variation1nstd223human GRCh38 chr2: 111,413,801-111,419,400 , GRCh37.p13 chr2: 112,171,378-112,176,977 MIR4435-2HG
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