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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv6890548copy number variation1nstd229human GRCh38 chr10: 93,867,543-94,344,766 , GRCh37.p13 chr10: 95,627,300-96,104,523 HDAC1P1, LOC107984255, 10 more genes
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6132060copy number variation1nstd213human GRCh37 chr10: 95,430,000-96,160,001 , GRCh38.p12 chr10: 93,670,243-94,400,244 LGI1, PLCE1, 14 more genes
    nsv6131986copy number variation1nstd213human GRCh37 chr10: 95,390,000-96,170,001 , GRCh38.p12 chr10: 93,630,243-94,410,244 PDE6C, LGI1, 16 more genes
    nsv6131898copy number variation1nstd213human GRCh37 chr10: 95,390,000-96,200,001 , GRCh38.p12 chr10: 93,630,243-94,440,244 PDE6C, LGI1, 16 more genes
    nsv6131820copy number variation1nstd213human GRCh37 chr10: 95,370,000-95,750,001 , GRCh38.p12 chr10: 93,610,243-93,990,244 PDE6C, LGI1, 7 more genes
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5916615copy number variation1nstd209human GRCh38 chr10: 93,876,944-93,938,329 , GRCh37.p13 chr10: 95,636,701-95,698,086 RAB11AP1, SLC35G1
    nsv5855562copy number variation1nstd209human GRCh38 chr10: 93,876,302-93,915,623 , GRCh37.p13 chr10: 95,636,059-95,675,380 RAB11AP1, SLC35G1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4348834copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 94,393,383-97,219,175 , GRCh38.p12 chr10: 92,633,626-95,459,418 CYP2C19, CYP2C8, 51 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3914138copy number variation1nstd102humanPathogenic GRCh37 chr10: 94,403,676-97,230,894 , GRCh38 chr10: 92,643,919-95,471,137 , NCBI36 chr10: 94,393,656-97,220,884 RPL7AP52, LGI1, 51 more genes
    nsv3912487copy number variation1nstd102humanPathogenic GRCh37 chr10: 94,386,437-99,514,859 , GRCh38 chr10: 92,626,680-97,755,102 , NCBI36 chr10: 94,376,417-99,504,849 ENTPD1-AS1, PLCE1, 105 more genes
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