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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121153copy number variation1nstd186human GRCh37 chr14: 65,527,158-65,527,428 , GRCh38.p12 chr14: 65,060,440-65,060,710 FNTB, MAX, 1 more genes
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5978661insertion1nstd209human GRCh38 chr14: 65,000,838-65,000,838 , GRCh37.p13 chr14: 65,467,556-65,467,556 CHURC1-FNTB, FNTB
    nsv5944786copy number variation1nstd209human GRCh38 chr14: 65,060,406-65,060,511 , GRCh37.p13 chr14: 65,527,124-65,527,229 FNTB, MAX, 1 more genes
    nsv5943867copy number variation1nstd209human GRCh38 chr14: 65,060,426-65,060,709 , GRCh37.p13 chr14: 65,527,144-65,527,427 FNTB, MAX, 1 more genes
    nsv5933324copy number variation1nstd209human GRCh38 chr14: 65,014,986-65,015,603 , GRCh37.p13 chr14: 65,481,704-65,482,321 FNTB, MAX, 1 more genes
    nsv5722196mobile element insertion1nstd211human GRCh38 chr14: 64,985,543-64,985,543 , GRCh37.p13 chr14: 65,452,261-65,452,261 FNTB, CHURC1-FNTB, 1 more genes
    nsv5718970mobile element insertion2nstd211human GRCh38 chr14: 65,039,843-65,039,843 , GRCh37.p13 chr14: 65,506,561-65,506,561 FNTB, MAX, 1 more genes
    nsv5716376mobile element insertion1nstd211human GRCh38 chr14: 65,049,920-65,049,920 , GRCh37.p13 chr14: 65,516,638-65,516,638 FNTB, MAX, 1 more genes
    nsv5706881mobile element insertion1nstd211human GRCh38 chr14: 64,989,608-64,989,608 , GRCh37.p13 chr14: 65,456,326-65,456,326 CHURC1-FNTB, FNTB
    nsv5699952mobile element insertion1nstd211human GRCh38 chr14: 65,015,433-65,015,433 , GRCh37.p13 chr14: 65,482,151-65,482,151 FNTB, MAX, 1 more genes
    nsv5599937copy number variation1nstd207human GRCh38 chr14: 65,060,426-65,060,709 , GRCh37.p13 chr14: 65,527,144-65,527,427 FNTB, MAX, 1 more genes
    nsv5563669mobile element insertion1nstd206human GRCh38 chr14: 65,039,843-65,039,894 , GRCh37.p13 chr14: 65,506,561-65,506,612 FNTB, MAX, 1 more genes
    nsv5563120mobile element insertion1nstd206human GRCh38 chr14: 64,985,554-64,985,594 , GRCh37.p13 chr14: 65,452,272-65,452,312 FNTB, CHURC1-FNTB, 1 more genes
    nsv5556816mobile element insertion1nstd206human GRCh38 chr14: 65,049,920-65,049,971 , GRCh37.p13 chr14: 65,516,638-65,516,689 FNTB, MAX, 1 more genes
    nsv5509520copy number variation1nstd206human GRCh38 chr14: 65,060,440-65,060,710 , GRCh37.p13 chr14: 65,527,158-65,527,428 MAX, CHURC1-FNTB, 1 more genes
    nsv5495835copy number variation1nstd206human GRCh38 chr14: 64,993,246-64,993,364 , GRCh37.p13 chr14: 65,459,964-65,460,082 CHURC1-FNTB, FNTB
    nsv5429160mobile element insertion1nstd206human GRCh38 chr14: 64,989,608-64,989,659 , GRCh37.p13 chr14: 65,456,326-65,456,377 CHURC1-FNTB, FNTB
    nsv5381825mobile element deletion2nstd186human GRCh37 chr14: 65,527,158-65,527,428 , GRCh38.p12 chr14: 65,060,440-65,060,710 FNTB, MAX, 1 more genes
    nsv5207529mobile element deletion1nstd204human GRCh37.p13 chr14: 65,527,155-65,527,431 , GRCh38.p13 chr14: 65,060,437-65,060,713 FNTB, MAX, 1 more genes
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