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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099178copy number variation1nstd231human GRCh38.p12 chr1: 13,573,893-15,986,640 , GRCh37 chr1: 13,900,388-16,313,135 CASP9, CD24P1, 43 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7095485copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,096,904-16,271,697 , GRCh38.p12 chr1: 15,770,409-15,945,202 ZBTB17, SPEN, 5 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv7048193inversion1nstd229human GRCh38 chr1: 9,469,567-16,279,388 , GRCh37.p13 chr1: 9,529,626-16,605,883 PRAMEF36P, HNRNPCL3, 193 more genes
    nsv6642577copy number variation1nstd229human GRCh38 chr1: 15,806,736-15,811,131 , GRCh37.p13 chr1: 16,133,231-16,137,626 UQCRHL
    nsv6642546copy number variation1nstd229human GRCh38 chr1: 15,699,908-15,843,215 , GRCh37.p13 chr1: 16,026,403-16,169,710 SLC25A34, RPL12P14, 7 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
    nsv6331016copy number variation1nstd223human GRCh38 chr1: 15,678,201-15,912,600 , GRCh37.p13 chr1: 16,004,696-16,239,095 SLC25A34-AS1, RPS16P1, 8 more genes
    nsv6315241copy number variation1nstd102humanLikely pathogenic GRCh38 chr1: 10,115,497-16,283,149 , GRCh37.p13 chr1: 10,175,555-16,609,644 CASP9, CD24P1, 173 more genes
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 RPL9P11, FAM131C2P, 466 more genes
    nsv6133923copy number variation2nstd213human GRCh37 chr1: 15,070,000-16,890,001 , GRCh38.p12 chr1: 14,743,504-16,563,506 CASP9, CD24P1, 63 more genes
    nsv6133589copy number variation1nstd213human GRCh37 chr1: 16,100,000-16,310,001 , GRCh38.p12 chr1: 15,773,505-15,983,506 ZBTB17, SPEN, 5 more genes
    nsv6133553copy number variation1nstd213human GRCh37 chr1: 15,070,000-16,830,001 , GRCh38.p12 chr1: 14,743,504-16,503,506 CASP9, CD24P1, 53 more genes
    nsv5981649copy number variation1nstd212human GRCh38 chr1: 15,699,908-15,843,225 , GRCh37.p13 chr1: 16,026,403-16,169,720 PLEKHM2, FBLIM1, 7 more genes
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5423911copy number variation1nstd206human GRCh38 chr1: 15,798,859-15,821,156 , GRCh37.p13 chr1: 16,125,354-16,147,651 UQCRHL
    nsv4895019copy number variation1nstd200human GRCh38 chr1: 15,798,829-15,821,176 , GRCh37.p13 chr1: 16,125,324-16,147,671 UQCRHL
    nsv4728309copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,041,431-21,295,864 , GRCh38.p12 chr1: 15,714,936-20,969,371 RNU1-6P, TRG-CCC4-1, 150 more genes
    nsv4453267copy number variation1nstd102humanUncertain significance GRCh37 chr1: 16,096,742-16,725,355 , GRCh38.p12 chr1: 15,770,247-16,398,860 RPL12P14, HSPB7, 21 more genes
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