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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148054copy number variation1nstd102humanPathogenic GRCh37 chr1: 142,535,935-157,648,813 , GRCh38.p12 chr1: 120,175,847-149,601,750 , TRN-GTT12-1, 266 more genes
    nsv7098839copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,405,854-147,597,284 , GRCh38.p12 chr1: 145,598,009-149,077,123 CCT8P1, LINC01719, 120 more genes
    nsv7098724copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,397,357-148,344,744 , GRCh38.p12 chr1: 144,536,526-148,549,211 , LOC105371217, 150 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7041638inversion1nstd229human GRCh38 chr1: 147,918,170-148,370,143 , GRCh37.p13 chr1|NW_003871055.3: 4,733,583-5,185,556 TRE-TTC6-1, TRQ-CTG9-1, 27 more genes
    nsv7038381inversion1nstd229human GRCh37.p13 chr1|NW_003871055.3: 5,105,420-5,185,431 , GRCh38 chr1: 148,290,007-148,370,018 , GRCh37.p13 chr1: 147,762,113-147,842,163 TRE-TTC6-1, LINC02806, 7 more genes
    nsv6641886copy number variation1nstd229human GRCh38 chr1: 148,360,411-148,360,465 , GRCh37.p13 chr1|NW_003871055.3: 5,175,824-5,175,878 RNVU1-1
    nsv6641729copy number variation1nstd229human GRCh38 chr1: 148,255,234-148,427,580 , GRCh37.p13 chr1|NW_003871055.3: 5,070,647-5,242,993 TRQ-CTG4-1, RNVU1-1, 17 more genes
    nsv6641408copy number variation1nstd229human GRCh38 chr1: 148,354,894-148,379,615 , GRCh37.p13 chr1|NW_003871055.3: 5,170,307-5,195,028 RNVU1-1, TRN-GTT23-1
    nsv6634349copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,157,447-148,016,122 , GRCh38.p12 chr1: 144,536,526-149,492,442 , TRN-GTT10-1, 170 more genes
    nsv6542731inversion1nstd223human GRCh38 chr1: 147,056,374-148,969,054 , GRCh37.p13 chr1|NW_003871055.3: 3,871,787-5,784,467 , LINC01731, 75 more genes
    nsv6333212copy number variation1nstd223human GRCh38 chr1: 148,361,501-148,368,100 , GRCh37.p13 chr1|NW_003871055.3: 5,176,914-5,183,513 RNVU1-1
    nsv6314909copy number variation1nstd102humanPathogenic GRCh38 chr1: 147,050,137-148,438,699 , GRCh37.p13 chr1|NW_003871055.3: 3,865,550-5,254,112 LOC101927468, MIR5087, 61 more genes
    nsv6290404copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,043,714-148,514,899 , GRCh38.p12 chr1: 144,536,526-148,549,211 , TRN-GTT9-2, 150 more genes
    nsv6290073copy number variation1nstd218human GRCh38.p12 chr1: 143,511,409-149,082,254 , GRCh37 chr1: 147,824,148-149,378,266 , BCL9, 215 more genes
    nsv6290072copy number variation1nstd218human GRCh38.p12 chr16: 34,632,766-36,225,009 , GRCh38.p12 chr7: 61,006,478-62,429,617 , GRCh38.p12 chr1: 146,347,888-148,514,931 , GRCh37 chr1: 147,806,599-149,821,717 , BCL9, 149 more genes
    nsv6290071copy number variation1nstd218human GRCh38.p12 chr1: 143,511,409-149,082,254 , GRCh37 chr1: 147,806,599-149,209,289 , BCL9, 215 more genes
    nsv6289910copy number variation1nstd102humanLikely pathogenic GRCh37.p13 chr1|NW_003871055.3: 2,417,359-5,412,838 , GRCh38 chr1: 145,601,946-148,597,425 BCL9, FMO5, 110 more genes
    nsv6109216inversion1nstd212human GRCh37.p13 chr1|NW_003871055.3: 3,128,345-6,166,149 , GRCh38 chr1: 146,312,932-149,350,736 , BCL9, 98 more genes
    nsv5885134copy number variation1nstd209human GRCh38 chr1: 143,707,729-148,368,205 , GRCh37.p13 chr1|NW_003871055.3: 523,142-5,183,618 , TRN-GTT22-1, 183 more genes
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