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Items: 1 to 20 of 125

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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
    nsv7047693inversion1nstd229human GRCh38 chr4: 76,264,843-76,851,623 , GRCh37.p13 chr4: 77,185,996-77,772,776 FAM47E-STBD1, LOC105377286, 13 more genes
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6754855copy number variation1nstd229human GRCh38 chr4: 76,283,049-76,562,694 , GRCh37.p13 chr4: 77,204,202-77,483,847 LOC105377286, FAM47E-STBD1, 8 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
    nsv6746757copy number variation1nstd229human GRCh38 chr4: 76,220,275-76,397,692 , GRCh37.p13 chr4: 77,141,428-77,318,845 STBD1, CCDC158, 5 more genes
    nsv6744707copy number variation1nstd229human GRCh38 chr4: 76,205,462-76,745,563 , GRCh37.p13 chr4: 77,126,615-77,666,716 CCDC158, RNU6-1000P, 14 more genes
    nsv6739195copy number variation1nstd229human GRCh38 chr4: 76,270,398-76,329,762 , GRCh37.p13 chr4: 77,191,551-77,250,915 FAM47E-STBD1, LOC105377286, 3 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
    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
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5377632translocation1nstd200human GRCh38 chr4: 76,309,841-76,309,841 , GRCh38 chr4: 76,318,214-76,318,214 , GRCh37.p13 chr4: 77,239,367-77,239,367 , GRCh37.p13 chr4: 77,230,994-77,230,994 STBD1, CCDC158, 2 more genes
    nsv5346745translocation1nstd200human GRCh38 chr4: 76,305,821-76,305,821 , GRCh38 chr4: 76,317,495-76,317,495 , GRCh37.p13 chr4: 77,226,974-77,226,974 , GRCh37.p13 chr4: 77,238,648-77,238,648 STBD1, CCDC158, 2 more genes
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