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Items: 1 to 20 of 1578

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2665966copy number variation1estd199human GRCh37 chr10: 84,566,631-84,621,062 , GRCh38.p12 chr10: 82,806,875-82,861,306 NRG3
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2666277copy number variation79estd199human GRCh37 chr7: 141,765,351-141,794,383 , GRCh38.p12 chr7: 142,065,551-142,094,583 , GRCh38.p12 chr7|NT_187562.1: 27,431-56,463 MGAM
    esv2676497copy number variation51estd199human GRCh37 chr4: 98,172,511-98,187,404 , GRCh38.p12 chr4: 97,251,360-97,266,253 STPG2
    esv2667088copy number variation20estd199human GRCh37 chr4: 98,172,511-98,187,404 , GRCh38.p12 chr4: 97,251,360-97,266,253 STPG2
    esv2657156copy number variation50estd199human GRCh37 chr21: 23,652,945-23,666,892 , GRCh38.p12 chr21: 22,280,625-22,294,572 , GRCh38.p12 chr21|NW_003315968.2: 184,854-198,801 LOC107985508
    esv2671383copy number variation1estd199human GRCh37 chr10: 16,700,568-16,714,200 , GRCh38.p12 chr10: 16,658,569-16,672,201 RSU1
    esv2669307copy number variation18estd199human GRCh37 chr6: 80,557,132-80,570,423 , GRCh38.p12 chr6: 79,847,415-79,860,706 LOC100422671
    esv2659146copy number variation109estd199human GRCh37 chrX: 154,790,189-154,803,312 , GRCh38.p12 chrX: 155,560,528-155,573,651 TMLHE
    esv2677364copy number variation34estd199human GRCh37 chr7: 91,029,645-91,042,742 , GRCh38.p12 chr7: 91,400,330-91,413,427 LINC02932
    esv2670787copy number variation158estd199human GRCh37 chr7: 151,134-160,557 , GRCh38.p12 chr7: 151,134-160,557 , GRCh38.p12 chr7|NT_187558.1: 106,939-119,904 , GRCh38.p12 chr7|NT_187653.1: 143,455-152,878 LINC03014
    esv2659442copy number variation87estd199human GRCh37 chr7: 150,945-159,992 , GRCh38.p12 chr7: 150,945-159,992 , GRCh38.p12 chr7|NT_187558.1: 106,750-119,335 , GRCh38.p12 chr7|NT_187653.1: 143,266-152,313 LINC03014
    esv2665606copy number variation90estd199human GRCh37 chr7: 91,031,083-91,042,584 , GRCh38.p12 chr7: 91,401,768-91,413,269 LINC02932
    esv2675519copy number variation112estd199human GRCh37 chr18: 66,745,594-66,756,999 , GRCh38.p12 chr18: 69,078,357-69,089,762 CCDC102B
    esv2659375copy number variation188estd199human GRCh37 chr21: 23,654,900-23,666,003 , GRCh38.p12 chr21: 22,282,580-22,293,683 , GRCh38.p12 chr21|NW_003315968.2: 186,809-197,912 LOC107985508
    esv2672284copy number variation80estd199human GRCh37 chr11: 107,233,995-107,244,392 , GRCh38.p12 chr11: 107,363,269-107,373,666 CWF19L2
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2669918copy number variation62estd199human GRCh37 chr1: 9,846,654-9,856,699 , GRCh38.p12 chr1: 9,786,596-9,796,641 CLSTN1
    esv2675979copy number variation520estd199human GRCh37 chr6: 53,924,803-53,934,828 , GRCh38.p12 chr6: 54,060,005-54,070,030 MLIP
    esv2661553copy number variation13estd199human GRCh37 chr11: 99,647,272-99,657,172 , GRCh38.p12 chr11: 99,776,541-99,786,441 CNTN5
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