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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052940inversion1nstd229human GRCh38 chr4: 73,455,263-76,320,440 , GRCh37.p13 chr4: 74,320,980-77,241,593 , RASSF6, 65 more genes
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6755239copy number variation1nstd229human GRCh38 chr4: 75,844,101-76,079,100 , GRCh37.p13 chr4: 76,765,254-77,000,253 LOC105377285, CXCL10, 8 more genes
    nsv6753012copy number variation1nstd229human GRCh38 chr4: 75,817,101-76,020,900 , GRCh37.p13 chr4: 76,738,254-76,942,053 LOC105377285, CXCL10, 8 more genes
    nsv6749929copy number variation1nstd229human GRCh38 chr4: 75,943,232-76,092,964 , GRCh37.p13 chr4: 76,864,385-77,014,117 ART3, SDAD1, 5 more genes
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6746322copy number variation1nstd229human GRCh38 chr4: 75,972,792-75,977,326 , GRCh37.p13 chr4: 76,893,945-76,898,479 SDAD1
    nsv6744945copy number variation1nstd229human GRCh38 chr4: 75,979,266-75,985,299 , GRCh37.p13 chr4: 76,900,419-76,906,452 SDAD1-AS1, SDAD1
    nsv6744421copy number variation1nstd229human GRCh38 chr4: 75,981,901-75,985,000 , GRCh37.p13 chr4: 76,903,054-76,906,153 SDAD1, SDAD1-AS1
    nsv6744001copy number variation1nstd229human GRCh38 chr4: 75,973,594-75,985,300 , GRCh37.p13 chr4: 76,894,747-76,906,453 SDAD1, SDAD1-AS1
    nsv6739808copy number variation1nstd229human GRCh38 chr4: 75,991,154-75,991,204 , GRCh37.p13 chr4: 76,912,307-76,912,357 SDAD1, SDAD1-AS1
    nsv6636459copy number variation1nstd102humanUncertain significance GRCh37 chr4: 76,872,306-77,038,327 , GRCh38.p12 chr4: 75,951,153-76,117,174 RPL36P8, SDAD1-AS1, 6 more genes
    nsv6630161copy number variation1nstd224human GRCh37 chr4: 76,750,356-76,892,610 , GRCh38.p12 chr4: 75,829,203-75,971,457 PPEF2, NAAA, 4 more genes
    nsv6629735copy number variation1nstd224human GRCh37 chr4: 76,885,365-79,465,559 , GRCh38.p12 chr4: 75,964,212-78,544,405 CCNI, NUP54, 54 more genes
    nsv6570597inversion1nstd223human GRCh38 chr4: 75,971,563-75,972,260 , GRCh37.p13 chr4: 76,892,716-76,893,413 SDAD1
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv6313715copy number variation1nstd102humanPathogenic GRCh37 chr4: 73,055,313-80,083,154 , GRCh38.p12 chr4: 72,189,596-79,162,000 CCNG2, FTLP9, 129 more genes
    nsv6313510copy number variation1nstd102humanPathogenic GRCh37 chr4: 75,737,340-91,131,156 , GRCh38.p12 chr4: 74,812,130-90,210,005 HIGD1AP13, CXCL11, 240 more genes
    nsv6311840copy number variation1nstd102humanPathogenic GRCh37 chr4: 76,481,293-77,700,330 , GRCh38.p12 chr4: 75,556,083-76,779,177 RNU2-16P, LOC105377285, 32 more genes
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