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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7148128copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 10,501-6,614,959 , GRCh38.p12 chr8: 60,501-6,757,438 ANGPT2, CLN8, 67 more genes
    nsv7064898inversion1nstd229human GRCh38 chr8: 232,683-363,798 , GRCh37.p13 chr8: 182,683-313,798 LOC105377773, ZNF596, 2 more genes
    nsv6837401copy number variation1nstd229human GRCh38 chr8: 247,024-255,706 , GRCh37.p13 chr8: 197,024-205,706 ZNF596
    nsv6836964copy number variation1nstd229human GRCh38 chr8: 228,673-285,340 , GRCh37.p13 chr8: 178,673-235,340 RPL23AP53, ZNF596, 1 more genes
    nsv6835642copy number variation1nstd229human GRCh38 chr8: 238,551-243,553 , GRCh37.p13 chr8: 188,551-193,553 ZNF596
    nsv6829104copy number variation1nstd229human GRCh38 chr8: 242,338-242,401 , GRCh37.p13 chr8: 192,338-192,401 ZNF596
    nsv6827043copy number variation1nstd229human GRCh38 chr8: 236,130-245,371 , GRCh37.p13 chr8: 186,130-195,371 ZNF596
    nsv6825443copy number variation1nstd229human GRCh38 chr8: 221,482-492,608 , GRCh37.p13 chr8: 171,482-442,608 ZNF596, RPL23AP53, 5 more genes
    nsv6820601copy number variation1nstd229human GRCh38 chr8: 233,827-267,605 , GRCh37.p13 chr8: 183,827-217,605 LOC101927566, ZNF596
    nsv6819623copy number variation1nstd229human GRCh38 chr8: 245,301-396,600 , GRCh37.p13 chr8: 195,301-346,600 FAM87A, LOC101927566, 2 more genes
    nsv6637122copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-4,608,757 , GRCh38.p12 chr8: 208,049-4,751,235 LOC105377779, LOC105377782, 40 more genes
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 ZNF705B, NATP, 357 more genes
    nsv6636940copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-10,965,627 , GRCh38.p12 chr8|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,049-11,108,117 HSPD1P3, LOC401442, 270 more genes
    nsv6636214copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-5,033,424 , GRCh38.p12 chr8: 208,049-5,175,902 RSL24D1P7, LOC105377775, 44 more genes
    nsv6634376copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-11,281,408 , GRCh38.p12 chr8: 208,048-11,423,899 DLGAP2-AS1, MIR124-1HG, 228 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6632786copy number variation1nstd224human GRCh37 chr8: 195,254-271,362 , GRCh38.p12 chr8: 245,254-321,362 LOC101927566, LOC105377773, 1 more genes
    nsv6632772copy number variation1nstd224human GRCh37 chr8: 163,226-3,063,043 , GRCh38.p12 chr8: 213,226-3,205,521 DLGAP2, FAM87A, 36 more genes
    nsv6632718copy number variation1nstd224human GRCh37 chr8: 195,682-304,569 , GRCh38.p12 chr8: 245,682-354,569 LOC101927566, LOC105377773, 1 more genes
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