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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7057605inversion1nstd229human GRCh38 chr1: 78,336,704-86,162,072 , GRCh37.p13 chr1: 78,802,388-86,627,755 LINC01712, LOC105378812, 74 more genes
    nsv7053103inversion1nstd229human GRCh38 chr1: 81,888,908-86,483,944 , GRCh37.p13 chr1: 82,354,593-86,949,627 C1orf52, DNAI3, 50 more genes
    nsv7049841inversion1nstd229human GRCh38 chr1: 84,848,723-86,345,988 , GRCh37.p13 chr1: 85,314,406-86,811,671 LOC105378825, MCOLN2, 19 more genes
    nsv7046575inversion1nstd229human GRCh38 chr1: 83,069,893-89,051,563 , GRCh37.p13 chr1: 83,535,576-89,517,246 LOC105378826, RN7SL583P, 87 more genes
    nsv7041571inversion1nstd229human GRCh38 chr1: 84,455,419-86,210,703 , GRCh37.p13 chr1: 84,921,102-86,676,386 GNG5, DNAI3, 25 more genes
    nsv6656416copy number variation1nstd229human GRCh38 chr1: 85,562,369-86,292,498 , GRCh37.p13 chr1: 86,028,052-86,758,181 RNA5SP51, LOC107985057, 7 more genes
    nsv6656169copy number variation1nstd229human GRCh38 chr1: 85,285,172-86,238,491 , GRCh37.p13 chr1: 85,750,855-86,704,174 DDAH1, ZNHIT6, 6 more genes
    nsv6655930copy number variation1nstd229human GRCh38 chr1: 84,869,727-85,731,312 , GRCh37.p13 chr1: 85,335,410-86,196,995 LOC105378821, C1orf52, 15 more genes
    nsv6655408copy number variation1nstd229human GRCh38 chr1: 85,579,142-85,579,388 , GRCh37.p13 chr1: 86,044,825-86,045,071 CCN1
    nsv6655405copy number variation1nstd229human GRCh38 chr1: 85,427,032-86,388,032 , GRCh37.p13 chr1: 85,892,715-86,853,715 LOC112268231, ZNHIT6, 10 more genes
    nsv6637014copy number variation1nstd102humanUncertain significance GRCh37 chr1: 85,878,203-86,849,716 , GRCh38.p12 chr1: 85,412,520-86,384,033 RNA5SP51, CCN1, 10 more genes
    nsv6317003copy number variation1nstd223human GRCh38 chr1: 85,562,366-86,292,497 , GRCh37.p13 chr1: 86,028,049-86,758,180 CCN1, DDAH1, 7 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv6161750copy number variation1nstd214human GRCh38 chr1: 85,580,462-85,580,549 , GRCh37.p13 chr1: 86,046,145-86,046,232 CCN1
    nsv6133666copy number variation1nstd213human GRCh37 chr1: 86,050,000-86,240,001 , GRCh38.p12 chr1: 85,584,317-85,774,318 CCN1, ZNHIT6, 4 more genes
    nsv5290303copy number variation1nstd204human GRCh37.p13 chr1: 86,042,368-86,044,768 , GRCh38.p13 chr1: 85,576,685-85,579,085 CCN1, DDAH1
    nsv5211937copy number variation1nstd204human GRCh38.p13 chr1: 85,576,366-85,579,371 , GRCh37.p13 chr1: 86,042,049-86,045,054 DDAH1, CCN1
    nsv5203395copy number variation1nstd204human GRCh38.p13 chr1: 85,576,801-85,580,900 , GRCh37.p13 chr1: 86,042,484-86,046,583 CCN1, DDAH1
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
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