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Items: 1 to 20 of 170

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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
    nsv5925678copy number variation1nstd209human GRCh38 chr10: 49,966,373-49,966,422 , GRCh37.p13 chr10|NW_004504302.1: 145,548-145,597 , GRCh37.p13 chr10: 51,726,133-51,726,182 TIMM23B, TIMM23B-AGAP6
    nsv5924422copy number variation1nstd209human GRCh38 chr10: 49,955,860-49,955,941 , GRCh37.p13 chr10|NW_004504302.1: 135,035-135,116 TIMM23B-AGAP6, TIMM23B
    nsv5917305copy number variation1nstd209human GRCh38 chr10: 49,965,728-49,966,109 , GRCh37.p13 chr10|NW_004504302.1: 144,903-145,284 , GRCh37.p13 chr10: 51,725,488-51,725,869 TIMM23B-AGAP6, TIMM23B
    nsv5917020copy number variation1nstd209human GRCh38 chr10: 49,964,272-49,964,511 , GRCh37.p13 chr10: 51,724,032-51,724,271 , GRCh37.p13 chr10|NW_004504302.1: 143,447-143,686 TIMM23B, TIMM23B-AGAP6
    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
    nsv5866030copy number variation1nstd209human GRCh37.p13 chr10|NW_004504302.1: 108,168-128,049 , GRCh38 chr10: 49,928,993-49,948,874 PARG, TIMM23B-AGAP6, 1 more genes
    nsv5599270copy number variation1nstd207human GRCh38 chr10: 49,965,465-49,965,594 , GRCh37.p13 chr10|NW_004504302.1: 144,640-144,769 , GRCh37.p13 chr10: 51,725,225-51,725,354 TIMM23B, TIMM23B-AGAP6
    nsv5597345copy number variation1nstd207human GRCh38 chr10: 49,964,164-49,964,287 , GRCh37.p13 chr10: 51,723,924-51,724,047 , GRCh37.p13 chr10|NW_004504302.1: 143,339-143,462 TIMM23B-AGAP6, TIMM23B
    nsv5487335copy number variation1nstd206human GRCh38 chr10: 49,965,762-49,966,274 , GRCh37.p13 chr10|NW_004504302.1: 144,937-145,449 , GRCh37.p13 chr10: 51,725,522-51,726,034 TIMM23B-AGAP6, TIMM23B
    nsv5483515copy number variation1nstd206human GRCh38 chr10: 47,586,000-50,754,368 , GRCh37.p13 chr10: 46,591,857-52,514,128 HMGB1P50, PARG, 65 more genes
    nsv5479740copy number variation1nstd206human GRCh37.p13 chr10|NW_004504302.1: 53,543-193,543 , GRCh38 chr10: 49,874,368-50,014,368 PARG, AGAP6, 5 more genes
    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
    nsv5316923copy number variation1nstd204human GRCh38.p13 chr10: 49,958,800-49,965,192 , GRCh37.p13 chr10|NW_004504302.1: 137,975-144,367 , GRCh37.p13 chr10: 51,719,650-51,724,952 TIMM23B, TIMM23B-AGAP6
    nsv5311380copy number variation1nstd204human GRCh37.p13 chr10|NW_004504302.1: 144,849-145,312 , GRCh37.p13 chr10: 51,725,434-51,725,897 , GRCh38.p13 chr10: 49,965,674-49,966,137 TIMM23B-AGAP6, TIMM23B
    nsv5259540copy number variation1nstd204human GRCh38.p13 chr10: 49,957,416-49,958,778 , GRCh37.p13 chr10|NW_004504302.1: 136,591-137,953 TIMM23B, TIMM23B-AGAP6
    nsv5255021copy number variation1nstd204human GRCh38.p13 chr10: 49,938,419-49,981,097 , GRCh37.p13 chr10|NW_004504302.1: 117,594-160,272 PARG, TIMM23B, 3 more genes
    nsv5253794copy number variation1nstd204human GRCh38.p13 chr10: 49,957,516-49,965,565 , GRCh37.p13 chr10: 51,719,660-51,725,325 , GRCh37.p13 chr10|NW_004504302.1: 136,691-144,740 TIMM23B-AGAP6, TIMM23B
    nsv5250990copy number variation1nstd204human GRCh38.p13 chr10: 49,956,401-49,957,100 , GRCh37.p13 chr10|NW_004504302.1: 135,576-136,275 TIMM23B-AGAP6, TIMM23B
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