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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148184copy number variation1nstd102humanPathogenic GRCh38 chr1: 243,221,458-248,919,110 , GRCh37.p13 chr1: 243,384,760-249,213,309 LOC105373271, LOC107985725, 153 more genes
    nsv7137502copy number variation1nstd232human GRCh37.p13 chr1: 248,524,937-248,525,020 , GRCh38.p12 chr1: 248,361,635-248,361,718 , GRCh38.p12 chr1|NT_187518.1: 9,609-9,692 , GRCh38.p12 chr1|NT_187646.1: 9,609-9,692 OR2T4
    nsv7099272copy number variation1nstd231human GRCh38.p12 chr1: 243,197,153-248,437,482 , GRCh37 chr1: 243,360,455-248,600,783 ADSS2, HNRNPU, 124 more genes
    nsv7098854copy number variation1nstd102humanPathogenic GRCh37 chr1: 245,704,069-249,212,562 , GRCh38.p12 chr1: 245,540,767-248,918,363 OR2X1P, OR14A2, 118 more genes
    nsv7047206inversion1nstd229human GRCh38 chr1: 248,129,213-248,587,211 , GRCh37.p13 chr1: 248,292,515-248,750,512 OR2M5, OR2T2, 21 more genes
    nsv7041109inversion1nstd229human GRCh38 chr1: 248,160,794-248,499,072 , GRCh37.p13 chr1: 248,324,096-248,662,373 OR2M2, OR2T12, 16 more genes
    nsv6676591copy number variation1nstd229human GRCh38 chr1: 247,742,306-248,679,100 , GRCh37.p13 chr1: 247,905,608-248,842,401 OR14A2, OR2T29, 50 more genes
    nsv6675868copy number variation1nstd229human GRCh38 chr1: 247,840,153-248,617,375 , GRCh37.p13 chr1: 248,003,455-248,780,676 CLK3P2, OR2T7, 41 more genes
    nsv6670346copy number variation1nstd229human GRCh38 chr1: 247,948,628-248,526,413 , GRCh37.p13 chr1: 248,111,930-248,689,714 OR2T5, LOC105373279, 30 more genes
    nsv6668582copy number variation1nstd229human GRCh38 chr1: 247,987,039-248,360,199 , GRCh37.p13 chr1: 248,150,341-248,523,501 OR2M4, OR2M7, 17 more genes
    nsv6665900copy number variation1nstd229human GRCh38 chr1: 247,656,440-248,785,565 , GRCh37.p13 chr1: 247,819,742-248,865,778 OR2X1P, OR3D1P, 60 more genes
    nsv6664072copy number variation1nstd229human GRCh38 chr1: 248,129,201-248,447,000 , GRCh37.p13 chr1: 248,292,503-248,610,301 OR2M2, OR2M4, 11 more genes
    nsv6663848copy number variation1nstd229human GRCh38 chr1: 247,940,888-248,395,106 , GRCh37.p13 chr1: 248,104,190-248,558,407 OR14C36, OR2L13, 21 more genes
    nsv6662027copy number variation1nstd229human GRCh38 chr1: 248,278,650-248,376,961 , GRCh37.p13 chr1: 248,441,952-248,540,262 OR2M7, OR14C36, 2 more genes
    nsv6660569copy number variation1nstd229human GRCh38 chr1: 248,359,936-248,361,991 , GRCh37.p13 chr1: 248,523,238-248,525,293 OR2T4
    nsv6659249copy number variation1nstd229human GRCh38 chr1: 247,556,814-248,422,746 , GRCh37.p13 chr1: 247,720,116-248,586,047 OR2L13, TRIM58, 44 more genes
    nsv6658281copy number variation1nstd229human GRCh38 chr1: 248,305,801-248,447,500 , GRCh37.p13 chr1: 248,469,103-248,610,801 OR2T4, OR2M7, 4 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636648copy number variation1nstd102humanPathogenic GRCh37 chr1: 239,910,960-249,224,684 , GRCh38.p12 chr1: 239,747,660-248,930,485 RFKP1, OR2T29, 206 more genes
    nsv6636282copy number variation1nstd102humanPathogenic GRCh37 chr1: 243,258,050-249,224,684 , GRCh38.p12 chr1: 243,094,748-248,930,485 AHCYP8, OR2M2, 154 more genes
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