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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
    nsv6757361copy number variation1nstd229human GRCh38 chr4: 76,000,639-76,041,717 , GRCh37.p13 chr4: 76,921,792-76,962,870 CXCL11, ART3, 4 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
    nsv6750615copy number variation1nstd229human GRCh38 chr4: 76,004,668-76,039,794 , GRCh37.p13 chr4: 76,925,821-76,960,947 ART3, CXCL9, 4 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
    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
    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
    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
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6135611copy number variation1nstd213human GRCh37 chr4: 76,190,000-77,120,001 , GRCh38.p12 chr4: 75,264,790-76,198,848 ART3, SCARB2, 21 more genes
    nsv6135361copy number variation1nstd213human GRCh37 chr4: 76,430,000-77,550,001 , GRCh38.p12 chr4: 75,504,790-76,628,848 ART3, SCARB2, 32 more genes
    nsv6078233insertion1nstd212human GRCh38 chr4: 76,019,526-76,019,526 , GRCh37.p13 chr4: 76,940,679-76,940,679 CXCL10, ART3
    nsv5964446insertion1nstd209human GRCh38 chr4: 76,019,526-76,019,526 , GRCh37.p13 chr4: 76,940,679-76,940,679 CXCL10, ART3
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