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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975449inversion1nstd209human GRCh38 chr8: 70,630,457-73,057,328 , GRCh37.p13 chr8: 71,542,692-73,969,563 , EYA1, 23 more genes
    nsv5547949insertion1nstd206human GRCh38 chr8: 72,743,852-72,743,899 , GRCh37.p13 chr8: 73,656,087-73,656,134 KCNB2, LOC101926908
    nsv5493276copy number variation1nstd206human GRCh38 chr8: 72,739,138-72,739,301 , GRCh37.p13 chr8: 73,651,373-73,651,536 LOC101926908, KCNB2
    nsv5487819copy number variation1nstd206human GRCh38 chr8: 72,747,831-72,747,881 , GRCh37.p13 chr8: 73,660,066-73,660,116 KCNB2, LOC101926908
    nsv5481809copy number variation1nstd206human GRCh38 chr8: 72,738,640-72,742,703 , GRCh37.p13 chr8: 73,650,875-73,654,938 KCNB2, LOC101926908
    nsv5256410copy number variation1nstd204human GRCh38.p13 chr8: 72,717,901-72,862,900 , GRCh37.p13 chr8: 73,630,136-73,775,135 KCNB2, LOC101926908
    nsv5253237copy number variation1nstd204human GRCh38.p13 chr8: 72,717,533-72,756,816 , GRCh37.p13 chr8: 73,629,768-73,669,051 LOC101926908, KCNB2
    nsv5252913copy number variation1nstd204human GRCh38.p13 chr8: 72,732,454-72,733,653 , GRCh37.p13 chr8: 73,644,689-73,645,888 LOC101926908, KCNB2
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv4965458copy number variation1nstd200human GRCh38 chr8: 72,322,061-73,662,211 , GRCh37.p13 chr8: 73,234,296-74,574,446 , RDH10-AS1, 21 more genes
    nsv4825899copy number variation1nstd200human GRCh37 chr8: 73,234,296-74,574,446 , GRCh38.p12 chr8: 72,322,061-73,662,211 , RDH10-AS1, 21 more genes
    nsv4555797insertion1nstd166human GRCh37.p13 chr8: 73,656,083-73,656,083 , GRCh38.p12 chr8: 72,743,848-72,743,848 KCNB2, LOC101926908
    nsv4525787copy number variation1nstd166human GRCh37.p13 chr8: 73,508,366-74,497,922 , GRCh38.p12 chr8: 72,596,131-73,585,687 PRXL2AP2, RDH10-AS1, 16 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv4165884copy number variation1nstd166human GRCh37.p13 chr8: 73,651,373-73,651,536 , GRCh38.p12 chr8: 72,739,138-72,739,301 LOC101926908, KCNB2
    nsv4163159copy number variation1nstd166human GRCh37.p13 chr8: 73,656,623-73,657,895 , GRCh38.p12 chr8: 72,744,388-72,745,660 LOC101926908, KCNB2
    nsv4153525copy number variation1nstd166human GRCh37.p13 chr8: 73,648,618-73,658,062 , GRCh38.p12 chr8: 72,736,383-72,745,827 LOC101926908, KCNB2
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