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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099248copy number variation1nstd231human GRCh38.p12 chr1: 172,685,012-173,856,229 , GRCh37 chr1: 172,654,152-173,825,367 TNFSF4, TNFSF18, 19 more genes
    nsv7055856inversion1nstd229human GRCh38 chr1: 172,753,749-173,357,724 , GRCh37.p13 chr1: 172,722,889-173,326,863 RPL26P11, AIMP1P2, 6 more genes
    nsv7049907inversion1nstd229human GRCh38 chr1: 173,049,762-173,049,798 , GRCh37.p13 chr1: 173,018,902-173,018,938 TNFSF18
    nsv6644862copy number variation1nstd229human GRCh38 chr1: 173,044,252-173,055,655 , GRCh37.p13 chr1: 173,013,392-173,024,795 TNFSF18
    nsv6644846copy number variation1nstd229human GRCh38 chr1: 172,689,801-173,072,375 , GRCh37.p13 chr1: 172,658,941-173,041,515 LOC107985225, SLC25A38P1, 3 more genes
    nsv6644717copy number variation1nstd229human GRCh38 chr1: 172,496,006-174,441,202 , GRCh37.p13 chr1: 172,465,146-174,410,340 RABGAP1L-DT, LOC100506023, 46 more genes
    nsv6544937inversion1nstd223human GRCh38 chr1: 172,815,509-173,473,302 , GRCh37.p13 chr1: 172,784,649-173,442,441 TNFSF4, TNFSF18, 8 more genes
    nsv6332091copy number variation1nstd223human GRCh38 chr1: 173,048,001-173,050,700 , GRCh37.p13 chr1: 173,017,141-173,019,840 TNFSF18
    nsv6313519copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,881,608-175,899,893 , GRCh38.p12 chr1: 171,912,468-175,930,757 RNU6-693P, PIGC, 73 more genes
    nsv6310765copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 171,605,065-173,962,123 , GRCh38.p12 chr1: 171,635,925-173,992,985 RNU6-157P, SNORD47, 60 more genes
    nsv6289891copy number variation1nstd102humanPathogenic GRCh38 chr1: 172,987,296-174,843,232 , GRCh37.p13 chr1: 172,956,436-174,812,370 LOC100302291, SNORD75, 41 more genes
    nsv6133940copy number variation1nstd213human GRCh37 chr1: 170,740,000-173,330,001 , GRCh38.p12 chr1: 170,770,859-173,360,862 TNFSF4, VAMP4, 50 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133600copy number variation1nstd213human GRCh37 chr1: 172,520,000-173,820,001 , GRCh38.p12 chr1: 172,550,860-173,850,863 FASLG, GOT2P2, 22 more genes
    nsv6133571copy number variation1nstd213human GRCh37 chr1: 172,670,000-173,070,001 , GRCh38.p12 chr1: 172,700,860-173,100,861 TNFSF18, SLC25A38P1, 3 more genes
    nsv6133567copy number variation1nstd213human GRCh37 chr1: 170,760,000-174,730,001 , GRCh38.p12 chr1: 170,790,859-174,760,863 FASLG, SERPINC1, 87 more genes
    nsv5981835copy number variation1nstd212human GRCh38 chr1: 172,946,635-173,165,928 , GRCh37.p13 chr1: 172,915,775-173,135,067 TNFSF18, GOT2P2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4898060copy number variation1nstd200human GRCh38 chr1: 173,044,251-173,055,655 , GRCh37.p13 chr1: 173,013,391-173,024,795 TNFSF18
    nsv4784685copy number variation1nstd200human GRCh37 chr1: 173,013,391-173,024,795 , GRCh38.p12 chr1: 173,044,251-173,055,655 TNFSF18
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