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Items: 1 to 20 of 1152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2667872copy number variation147estd199human GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952 DNAH14
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2661656copy number variation43estd199human GRCh37 chr16: 55,794,745-55,823,292 , GRCh38.p12 chr16: 55,760,833-55,789,380 CES1P1
    esv2665251copy number variation49estd199human GRCh37 chr9: 40,135,245-40,158,892 , GRCh38.p12 chr9: 67,396,719-67,420,087 LOC101927602
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2671922copy number variation12estd199human GRCh37 chr3: 89,531,431-89,547,075 , GRCh38.p12 chr3: 89,482,281-89,497,925 EPHA3
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    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
    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
    esv2675866copy number variation315estd199human GRCh37 chr9: 113,024,576-113,037,093 , GRCh38.p12 chr9: 110,262,296-110,274,813 LOC107987114
    esv2663832copy number variation109estd199human GRCh37 chr4: 118,579,966-118,591,119 , GRCh38.p12 chr4: 117,658,811-117,669,964 LINC01378
    esv2670942copy number variation57estd199human GRCh37 chr10: 18,913,663-18,923,800 , GRCh38.p12 chr10: 18,624,734-18,634,871 NSUN6
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2675979copy number variation520estd199human GRCh37 chr6: 53,924,803-53,934,828 , GRCh38.p12 chr6: 54,060,005-54,070,030 MLIP
    esv2662536copy number variation311estd199human GRCh37 chr6: 72,863,851-72,873,540 , GRCh38.p12 chr6: 72,154,148-72,163,837 RIMS1
    esv2660655copy number variation49estd199human GRCh37 chr20: 62,949,733-62,959,201 , GRCh38.p12 chr20: 64,318,380-64,327,848 IQSEC3P3
    esv2663931copy number variation243estd199human GRCh37 chr4: 138,092,000-138,100,631 , GRCh38.p12 chr4: 137,170,846-137,179,477 LINC02511
    esv2659844copy number variation372estd199human GRCh37 chr6: 53,925,724-53,934,162 , GRCh38.p12 chr6: 54,060,926-54,069,364 MLIP
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