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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7054208inversion1nstd229human GRCh38 chr4: 91,987,159-94,765,936 , GRCh37.p13 chr4: 92,908,310-95,687,087 SMARCAD1-DT, BMPR1B-DT, 14 more genes
    nsv7047278inversion1nstd229human GRCh38 chr4: 92,017,603-94,765,933 , GRCh37.p13 chr4: 92,938,754-95,687,084 ATOH1, LNCPRESS2, 14 more genes
    nsv6757543copy number variation1nstd229human GRCh38 chr4: 94,118,378-94,124,128 , GRCh37.p13 chr4: 95,039,529-95,045,279 SMARCAD1-DT
    nsv6755464copy number variation1nstd229human GRCh38 chr4: 94,165,940-94,172,453 , GRCh37.p13 chr4: 95,087,091-95,093,604 SMARCAD1-DT
    nsv6755291copy number variation1nstd229human GRCh38 chr4: 91,791,218-94,840,947 , GRCh37.p13 chr4: 92,712,369-95,762,098 HMGB3P15, RPL35AP11, 15 more genes
    nsv6755035copy number variation1nstd229human GRCh38 chr4: 94,172,177-94,174,791 , GRCh37.p13 chr4: 95,093,328-95,095,942 SMARCAD1-DT
    nsv6753863copy number variation1nstd229human GRCh38 chr4: 94,124,109-94,133,342 , GRCh37.p13 chr4: 95,045,260-95,054,493 SMARCAD1-DT
    nsv6753120copy number variation1nstd229human GRCh38 chr4: 94,016,966-94,422,680 , GRCh37.p13 chr4: 94,938,117-95,343,831 SMARCAD1, HMGB3P15, 3 more genes
    nsv6750939copy number variation1nstd229human GRCh38 chr4: 94,101,861-94,117,563 , GRCh37.p13 chr4: 95,023,012-95,038,714 SMARCAD1-DT
    nsv6750292copy number variation1nstd229human GRCh38 chr4: 94,065,373-94,822,571 , GRCh37.p13 chr4: 94,986,524-95,743,722 HPGDS, BMPR1B-DT, 6 more genes
    nsv6748880copy number variation1nstd229human GRCh38 chr4: 92,755,485-94,331,886 , GRCh37.p13 chr4: 93,676,636-95,253,037 RACK1P3, SMARCAD1, 6 more genes
    nsv6746149copy number variation1nstd229human GRCh38 chr4: 94,115,369-94,165,265 , GRCh37.p13 chr4: 95,036,520-95,086,416 SMARCAD1-DT
    nsv6745533copy number variation1nstd229human GRCh38 chr4: 94,182,315-94,185,062 , GRCh37.p13 chr4: 95,103,466-95,106,213 SMARCAD1-DT
    nsv6744901copy number variation1nstd229human GRCh38 chr4: 94,116,934-94,142,902 , GRCh37.p13 chr4: 95,038,085-95,064,053 SMARCAD1-DT
    nsv6742777copy number variation1nstd229human GRCh38 chr4: 93,917,753-94,124,232 , GRCh37.p13 chr4: 94,838,904-95,045,383 SMARCAD1-DT
    nsv6741346copy number variation1nstd229human GRCh38 chr4: 94,136,741-94,142,570 , GRCh37.p13 chr4: 95,057,892-95,063,721 SMARCAD1-DT
    nsv6740938copy number variation1nstd229human GRCh38 chr4: 94,199,279-94,258,392 , GRCh37.p13 chr4: 95,120,430-95,179,543 SMARCAD1, SMARCAD1-DT
    nsv6740706copy number variation1nstd229human GRCh38 chr4: 94,163,079-94,167,514 , GRCh37.p13 chr4: 95,084,230-95,088,665 SMARCAD1-DT
    nsv6739972copy number variation1nstd229human GRCh38 chr4: 94,191,775-94,194,691 , GRCh37.p13 chr4: 95,112,926-95,115,842 HMGB3P15, SMARCAD1-DT
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