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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148249copy number variation1nstd102humanPathogenic GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322 TRDN-AS1, LOC100420743, 179 more genes
    nsv7137202copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 112,713,854-124,105,184 , GRCh38.p12 chr6: 112,392,652-123,784,039 COL10A1, FABP7, 129 more genes
    nsv7057090inversion1nstd229human GRCh38 chr6: 112,695,234-116,359,280 , GRCh37.p13 chr6: 113,016,436-116,680,443 MARCKS, TSPYL1, 42 more genes
    nsv7045667inversion1nstd229human GRCh38 chr6: 113,913,191-113,913,217 , GRCh37.p13 chr6: 114,234,355-114,234,381 LINC02880
    nsv7043912inversion1nstd229human GRCh38 chr6: 113,606,593-119,197,751 , GRCh37.p13 chr6: 113,927,795-119,518,916 TPI1P3, CALHM5, 73 more genes
    nsv6815317copy number variation1nstd229human GRCh38 chr6: 110,458,576-114,390,336 , GRCh37.p13 chr6: 110,779,779-114,711,500 LOC105377956, LOC102724646, 79 more genes
    nsv6811299copy number variation1nstd229human GRCh38 chr6: 113,420,301-113,917,400 , GRCh37.p13 chr6: 113,741,503-114,238,564 RPL30P8, LINC02880, 5 more genes
    nsv6809523copy number variation1nstd229human GRCh38 chr6: 113,902,781-113,903,871 , GRCh37.p13 chr6: 114,223,945-114,225,035 LINC02880
    nsv6806609copy number variation1nstd229human GRCh38 chr6: 113,920,221-113,922,604 , GRCh37.p13 chr6: 114,241,385-114,243,768 LINC02880
    nsv6805368copy number variation1nstd229human GRCh38 chr6: 113,869,201-113,903,000 , GRCh37.p13 chr6: 114,190,366-114,224,164 LINC02880, MROCKI
    nsv6803384copy number variation1nstd229human GRCh38 chr6: 113,907,873-113,911,947 , GRCh37.p13 chr6: 114,229,037-114,233,111 LINC02880
    nsv6800348copy number variation1nstd229human GRCh38 chr6: 113,909,401-113,913,000 , GRCh37.p13 chr6: 114,230,565-114,234,164 LINC02880
    nsv6618491copy number variation1nstd223human GRCh38 chr6: 113,915,247-113,915,704 , GRCh37.p13 chr6: 114,236,411-114,236,868 LINC02880
    nsv6606808copy number variation1nstd223human GRCh38 chr6: 111,642,175-118,933,374 , GRCh37.p13 chr6: 111,963,378-119,254,539 COL10A1, LOC105377952, 106 more genes
    nsv6600477copy number variation1nstd223human GRCh38 chr6: 113,902,781-113,903,875 , GRCh37.p13 chr6: 114,223,945-114,225,039 LINC02880
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6313613copy number variation1nstd102humanUncertain significance GRCh37 chr6: 110,472,732-114,762,836 , GRCh38.p12 chr6: 110,151,529-114,441,672 LOC107986522, TUBE1, 87 more genes
    nsv6281121insertion1nstd214human GRCh38 chr6: 113,906,443-113,906,443 , GRCh37.p13 chr6: 114,227,607-114,227,607 LINC02880
    nsv6074383insertion1nstd212human GRCh38 chr6: 113,906,419-113,906,419 , GRCh37.p13 chr6: 114,227,583-114,227,583 LINC02880
    nsv6069435insertion1nstd212human GRCh38 chr6: 113,906,409-113,906,409 , GRCh37.p13 chr6: 114,227,573-114,227,573 LINC02880
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