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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903950copy number variation1nstd209human GRCh38 chr6: 36,710,587-36,710,657 , GRCh37.p13 chr6: 36,678,364-36,678,434 RAB44
    nsv5891739copy number variation1nstd209human GRCh38 chr6: 36,705,601-36,707,092 , GRCh37.p13 chr6: 36,673,378-36,674,869 RAB44
    nsv5890099copy number variation1nstd209human GRCh38 chr6: 36,696,590-36,696,647 , GRCh37.p13 chr6: 36,664,367-36,664,424 RAB44
    nsv5638186insertion1nstd207human GRCh38 chr6: 36,715,102-36,715,102 , GRCh37.p13 chr6: 36,682,879-36,682,879 RAB44
    nsv5581064copy number variation1nstd207human GRCh38 chr6: 36,710,587-36,710,657 , GRCh37.p13 chr6: 36,678,364-36,678,434 RAB44
    nsv5566811copy number variation1nstd207human GRCh38 chr6: 36,696,590-36,696,647 , GRCh37.p13 chr6: 36,664,367-36,664,424 RAB44
    nsv5464375copy number variation1nstd206human GRCh38 chr6: 36,732,782-36,737,733 , GRCh37.p13 chr6: 36,700,559-36,705,510 GPR166P, RAB44
    nsv5460302copy number variation1nstd206human GRCh38 chr6: 36,711,789-36,712,024 , GRCh37.p13 chr6: 36,679,566-36,679,801 RAB44
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5031134inversion1nstd200human GRCh38 chr6: 35,178,266-40,407,996 , GRCh37.p13 chr6: 35,146,043-40,375,735 , LOC105375040, 114 more genes
    nsv4940918copy number variation1nstd200human GRCh38 chr6: 36,732,782-36,737,733 , GRCh37.p13 chr6: 36,700,559-36,705,510 RAB44, GPR166P
    nsv4940917copy number variation1nstd200human GRCh38 chr6: 36,727,294-36,745,783 , GRCh37.p13 chr6: 36,695,071-36,713,560 RAB44, GPR166P, 1 more genes
    nsv4940916copy number variation1nstd200human GRCh38 chr6: 36,727,091-36,729,737 , GRCh37.p13 chr6: 36,694,868-36,697,514 RAB44
    nsv4940915copy number variation1nstd200human GRCh38 chr6: 36,707,683-36,708,387 , GRCh37.p13 chr6: 36,675,460-36,676,164 RAB44
    nsv4940914copy number variation1nstd200human GRCh38 chr6: 36,705,795-36,706,026 , GRCh37.p13 chr6: 36,673,572-36,673,803 RAB44
    nsv4940913copy number variation1nstd200human GRCh38 chr6: 36,705,602-36,707,093 , GRCh37.p13 chr6: 36,673,379-36,674,870 RAB44
    nsv4940912copy number variation1nstd200human GRCh38 chr6: 36,698,893-36,698,996 , GRCh37.p13 chr6: 36,666,670-36,666,773 RAB44
    nsv4934632copy number variation1nstd200human GRCh38 chr6: 36,405,862-36,962,727 , GRCh37.p13 chr6: 36,373,639-36,930,503 RN7SL502P, PPIL1, 17 more genes
    nsv4872414inversion1nstd200human GRCh37 chr6: 35,146,053-40,375,735 , GRCh38.p12 chr6: 35,178,276-40,407,996 , RPL36P9, 114 more genes
    nsv4816035copy number variation1nstd200human GRCh37 chr6: 36,675,460-36,676,164 , GRCh38.p12 chr6: 36,707,683-36,708,387 RAB44
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