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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5964939insertion1nstd209human GRCh38 chr4: 143,381,496-143,381,496 , GRCh37.p13 chr4: 144,302,649-144,302,649 GAB1
    nsv5947560insertion1nstd209human GRCh38 chr4: 143,373,852-143,373,852 , GRCh37.p13 chr4: 144,295,005-144,295,005 GAB1
    nsv5903333copy number variation1nstd209human GRCh38 chr4: 143,419,101-143,419,725 , GRCh37.p13 chr4: 144,340,254-144,340,878 GAB1
    nsv5902652copy number variation1nstd209human GRCh38 chr4: 143,386,771-143,387,369 , GRCh37.p13 chr4: 144,307,924-144,308,522 GAB1
    nsv5895870copy number variation1nstd209human GRCh38 chr4: 143,366,813-143,367,000 , GRCh37.p13 chr4: 144,287,966-144,288,153 GAB1
    nsv5891701copy number variation1nstd209human GRCh38 chr4: 143,377,298-143,378,590 , GRCh37.p13 chr4: 144,298,451-144,299,743 GAB1
    nsv5677687mobile element insertion2nstd211human GRCh38 chr4: 143,381,510-143,381,510 , GRCh37.p13 chr4: 144,302,663-144,302,663 GAB1
    nsv5612568insertion1nstd207human GRCh38 chr4: 143,363,340-143,363,340 , GRCh37.p13 chr4: 144,284,493-144,284,493 GAB1
    nsv5606464insertion1nstd207human GRCh38 chr4: 143,373,864-143,373,864 , GRCh37.p13 chr4: 144,295,017-144,295,017 GAB1
    nsv5563171sequence alteration1nstd206human GRCh38 chr4: 143,371,528-143,371,560 , GRCh37.p13 chr4: 144,292,681-144,292,713 GAB1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5471006copy number variation1nstd206human GRCh38 chr4: 143,368,747-143,368,800 , GRCh37.p13 chr4: 144,289,900-144,289,953 GAB1
    nsv5466175copy number variation1nstd206human GRCh38 chr4: 143,386,771-143,387,370 , GRCh37.p13 chr4: 144,307,924-144,308,523 GAB1
    nsv5464800copy number variation1nstd206human GRCh38 chr4: 143,377,302-143,378,591 , GRCh37.p13 chr4: 144,298,455-144,299,744 GAB1
    nsv5463479copy number variation1nstd206human GRCh38 chr4: 143,445,894-143,455,512 , GRCh37.p13 chr4: 144,367,047-144,376,665 GAB1
    nsv5458410copy number variation1nstd206human GRCh38 chr4: 143,366,816-143,367,001 , GRCh37.p13 chr4: 144,287,969-144,288,154 GAB1
    nsv5408697mobile element insertion1nstd206human GRCh38 chr4: 143,381,510-143,381,561 , GRCh37.p13 chr4: 144,302,663-144,302,714 GAB1
    nsv5377667translocation1nstd200human GRCh38 chr4: 143,343,178-143,343,178 , GRCh38 chr4: 143,350,800-143,350,800 , GRCh37.p13 chr4: 144,264,331-144,264,331 , GRCh37.p13 chr4: 144,271,953-144,271,953 MIR3139, GAB1
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