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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
    nsv6641020copy number variation1nstd229human GRCh38 chr1: 120,955,878-120,959,780 , GRCh37.p13 chr1|NW_003871056.3: 1,027,452-1,031,354 LINC00623
    nsv6327370copy number variation1nstd223human GRCh38 chr1: 120,955,874-120,959,780 , GRCh37.p13 chr1|NW_003871056.3: 1,027,448-1,031,354 LINC00623
    nsv6313671copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985 GAPDHP23, RNA5SP56, 243 more genes
    nsv6138586copy number variation1nstd206human GRCh38 chr1: 120,579,835-120,924,200 , GRCh37.p13 chr1|NW_003871056.3: 651,409-995,774 , PPIAL4A, 8 more genes
    nsv5827627copy number variation2nstd209human GRCh38 chr1: 120,921,050-120,922,624 , GRCh37.p13 chr1|NW_003871056.3: 992,624-994,198 LINC00623
    nsv5433692copy number variation1nstd206human GRCh38 chr1: 120,953,835-120,959,835 , GRCh37.p13 chr1|NW_003871056.3: 1,025,409-1,031,409 , LINC00623
    nsv5427936copy number variation1nstd206human GRCh37.p13 chr1|NW_003871056.3: 897,409-995,409 , GRCh38 chr1: 120,825,835-120,923,835 , GRCh37.p13 chr1: 149,509,647-149,587,125 PPIAL4A, LINC00623, 4 more genes
    nsv5423431copy number variation1nstd206human GRCh38 chr1: 120,937,328-120,937,416 , GRCh37.p13 chr1|NW_003871056.3: 1,008,902-1,008,990 LINC00623
    nsv5415604copy number variation1nstd206human GRCh38 chr1: 120,938,317-120,938,889 , GRCh37.p13 chr1|NW_003871056.3: 1,009,891-1,010,463 LINC00623
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5219710copy number variation1nstd204human GRCh38.p13 chr1: 120,913,701-120,917,500 , GRCh37.p13 chr1|NW_003871056.3: 985,275-989,074 LINC00623, LOC100996720
    nsv5219669copy number variation1nstd204human GRCh38.p13 chr1: 120,922,501-120,922,900 , GRCh37.p13 chr1|NW_003871056.3: 994,075-994,474 LINC00623
    nsv5219167copy number variation1nstd204human GRCh38.p13 chr1: 120,919,201-120,920,900 , GRCh37.p13 chr1|NW_003871056.3: 990,775-992,474 LINC00623
    nsv5218403copy number variation1nstd204human GRCh38.p13 chr1: 120,948,101-120,948,700 , GRCh37.p13 chr1|NW_003871056.3: 1,019,675-1,020,274 LINC00623
    nsv5217244copy number variation1nstd204human GRCh38.p13 chr1: 120,940,191-120,947,313 , GRCh37.p13 chr1|NW_003871056.3: 1,011,765-1,018,887 RNVU1-4, LINC00623
    nsv5215119copy number variation1nstd204human GRCh38.p13 chr1: 120,919,201-120,925,000 , GRCh37.p13 chr1|NW_003871056.3: 990,775-996,574 LINC00623
    nsv5213943copy number variation1nstd204human GRCh38.p13 chr1: 120,910,201-120,917,000 , GRCh37.p13 chr1|NW_003871056.3: 981,775-988,574 LINC00623, LOC100996720
    nsv5213728copy number variation1nstd204human GRCh38.p13 chr1: 120,920,501-120,924,200 , GRCh37.p13 chr1|NW_003871056.3: 992,075-995,774 LINC00623
    nsv5213454copy number variation1nstd204human GRCh38.p13 chr1: 120,927,301-120,928,000 , GRCh37.p13 chr1|NW_003871056.3: 998,875-999,574 LINC00623
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