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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112736copy number variation1nstd102humanPathogenic GRCh37 chr10: 48,301,535-51,807,296 , GRCh38.p12 chr10: 45,999,930-49,959,916 SHLD2P3, LOC100420617, 95 more genes
    nsv5967453insertion1nstd209human GRCh38 chr10: 45,993,244-45,993,244 , GRCh37.p13 chr10|NW_003871068.1: 264,359-264,359 TIMM23
    nsv5917415copy number variation1nstd209human GRCh37.p13 chr10|NW_003871068.1: 219,185-249,019 , GRCh38 chr10: 45,948,070-45,977,904 PARGP1, TIMM23, 1 more genes
    nsv5916113copy number variation1nstd209human GRCh38 chr10: 45,791,488-50,132,032 , GRCh37.p13 chr10|NW_003871068.1: 62,603-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,891,792 , LINC02675, 111 more genes
    nsv5914502copy number variation1nstd209human GRCh38 chr10: 45,768,833-50,109,449 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 39,948-2,281,126 , AGAP13P, 111 more genes
    nsv5858825copy number variation1nstd209human GRCh38 chr10: 46,003,927-46,013,409 , GRCh37.p13 chr10|NW_003871068.1: 275,042-284,524 , GRCh37.p13 chr10: 51,582,413-51,591,895 TIMM23, NCOA4
    nsv5857381copy number variation1nstd209human GRCh37.p13 chr10|NW_003871068.1: 226,201-249,015 , GRCh38 chr10: 45,955,086-45,977,900 PARGP1, TIMM23, 1 more genes
    nsv5853590copy number variation1nstd209human GRCh38 chr10: 45,972,971-45,975,251 , GRCh37.p13 chr10|NW_003871068.1: 244,086-246,366 TIMM23
    nsv5628217insertion1nstd207human GRCh38 chr10: 45,994,043-45,994,043 , GRCh37.p13 chr10|NW_003871068.1: 265,158-265,158 TIMM23
    nsv5591175copy number variation1nstd207human GRCh38 chr10: 45,997,277-45,997,361 , GRCh37.p13 chr10|NW_003871068.1: 268,392-268,476 TIMM23
    nsv5558939sequence alteration1nstd206human GRCh38 chr10: 45,994,043-45,994,053 , GRCh37.p13 chr10|NW_003871068.1: 265,158-265,168 TIMM23
    nsv5489018copy number variation1nstd206human GRCh38 chr10: 45,680,265-46,362,265 , GRCh37.p13 chr10: 46,224,334-47,733,482 , GRCh37.p13 chr10|NW_003871068.1: 1-633,380 PARGP1-AGAP4, RPL35AP23, 20 more genes
    nsv5485531copy number variation1nstd206human GRCh38 chr10: 45,740,265-46,020,265 , GRCh37.p13 chr10|NW_003871068.1: 11,380-291,380 SNORA74C-1, RNA5SP310, 8 more genes
    nsv5479567copy number variation1nstd206human GRCh38 chr10: 45,994,224-45,995,973 , GRCh37.p13 chr10|NW_003871068.1: 265,339-267,088 TIMM23
    nsv5380941copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,033,586-52,417,694 , GRCh38.p12 chr10: 45,999,930-49,959,916 CHAT, CTSLP2, 95 more genes
    nsv5347626translocation1nstd200human GRCh38 chr10: 45,997,100-45,997,100 , GRCh38 chr10: 45,997,255-45,997,255 , GRCh37.p13 chr10|NW_003871068.1: 268,215-268,215 , GRCh37.p13 chr10|NW_003871068.1: 268,370-268,370 TIMM23
    nsv5251970copy number variation1nstd204human GRCh37.p13 chr10|NW_003871068.1: 109,816-283,115 , GRCh38.p13 chr10: 45,838,701-46,012,000 NCOA4, AGAP4, 6 more genes
    nsv5250821copy number variation1nstd204human GRCh38.p13 chr10: 46,002,490-46,004,489 , GRCh37.p13 chr10: 51,591,333-51,593,332 , GRCh37.p13 chr10|NW_003871068.1: 273,605-275,604 TIMM23, NCOA4
    nsv5248280copy number variation1nstd204human GRCh38.p13 chr10: 45,974,354-45,976,916 , GRCh37.p13 chr10|NW_003871068.1: 245,469-248,031 TIMM23
    nsv5244892copy number variation1nstd204human GRCh38.p13 chr10: 45,971,246-45,972,707 , GRCh37.p13 chr10|NW_003871068.1: 242,361-243,822 TIMM23, PARGP1-AGAP4, 1 more genes
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