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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5913193copy number variation1nstd209human GRCh38 chr9: 21,077,427-21,077,912 , GRCh37.p13 chr9: 21,077,426-21,077,911 IFNB1
    esv3123937copy number variation1estd209human GRCh37 chr9: 21,076,198-21,076,199 , GRCh38.p12 chr9: 21,076,199-21,076,200 IFNB1
    esv2645876copy number variation1estd197human NCBI36 chr9: 21,066,205-21,066,205 , GRCh37.p13 chr9: 21,076,205-21,076,205 , GRCh38.p12 chr9: 21,076,206-21,076,206 IFNB1
    esv2598803copy number variation1estd197human NCBI36 chr9: 21,066,199-21,066,199 , GRCh37.p13 chr9: 21,076,199-21,076,199 , GRCh38.p12 chr9: 21,076,200-21,076,200 IFNB1
    esv1976992copy number variation1estd194human NCBI36 chr9: 21,066,199-21,066,200 , GRCh37.p13 chr9: 21,076,199-21,076,200 , GRCh38.p12 chr9: 21,076,200-21,076,201 IFNB1
    esv1650711copy number variation1estd22human NCBI36 chr9: 21,066,204-21,066,205 , GRCh37.p13 chr9: 21,076,204-21,076,205 , GRCh38.p12 chr9: 21,076,205-21,076,206 IFNB1
    nsv6633630copy number variation1nstd224human GRCh37 chr9: 21,056,582-21,080,518 , GRCh38.p12 chr9: 21,056,583-21,080,519 IFNB1, IFNNP1
    nsv4368729copy number variation1nstd173human GRCh37 chr9: 21,054,986-21,093,198 , GRCh38.p12 chr9: 21,054,987-21,093,199 IFNB1, IFNNP1
    nsv892732copy number variation1nstd71human NCBI36 chr9: 21,044,806-21,079,434 , GRCh37.p13 chr9: 21,054,806-21,089,434 , GRCh38.p12 chr9: 21,054,807-21,089,435 IFNB1, IFNNP1
    nsv6859216copy number variation1nstd229human GRCh38 chr9: 21,037,402-21,089,029 , GRCh37.p13 chr9: 21,037,401-21,089,028 IFNB1, IFNNP1, 1 more genes
    nsv6860296copy number variation1nstd229human GRCh38 chr9: 21,053,901-21,095,300 , GRCh37.p13 chr9: 21,053,900-21,095,299 IFNB1, IFNNP1, 1 more genes
    nsv1161847copy number variation1nstd111human GRCh38.p12 chr9: 21,006,309-21,091,241 , GRCh37 chr9: 21,006,308-21,091,240 IFNB1, HACD4, 2 more genes
    nsv613753copy number variation1nstd54human NCBI36 chr9: 21,027,771-21,072,814 , GRCh37.p13 chr9: 21,037,771-21,082,814 , GRCh38.p12 chr9: 21,037,772-21,082,815 IFNB1, IFNNP1, 1 more genes
    nsv466294copy number variation1nstd27human NCBI35 chr9: 21,027,771-21,072,814 , GRCh37.p13 chr9: 21,037,771-21,082,814 , GRCh38.p12 chr9: 21,037,772-21,082,815 IFNB1, IFNNP1, 1 more genes
    nsv3914932copy number variation1nstd102humanPathogenic NCBI36 chr9: 19,554,273-28,096,620 , GRCh37 chr9: 19,564,273-28,106,620 , GRCh38 chr9: 19,564,275-28,106,622 IFNB1, LINC01241, 103 more genes
    nsv3896464copy number variation1nstd102humanPathogenic GRCh37 chr9: 20,951,885-22,447,709 , GRCh38.p12 chr9: 20,951,886-22,447,710 IFNB1, MIR31HG, 44 more genes
    nsv4350534copy number variation1nstd102humanPathogenic GRCh37 chr9: 20,715,401-22,136,489 , GRCh38.p12 chr9: 20,715,402-22,136,490 IFNB1, IFNW1, 45 more genes
    nsv3901679copy number variation1nstd102humanPathogenic GRCh37 chr9: 20,834,837-22,101,120 , GRCh38.p12 chr9: 20,834,838-22,101,121 IFNB1, IFNA5, 43 more genes
    nsv3912247copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981 IFNB1, ALOX15P2, 2184 more genes
    nsv3890420copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797 IFNB1, TBC1D13, 2183 more genes
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