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Items: 1 to 20 of 803

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142934insertion1nstd232human GRCh37.p13 chr1: 1,154,014-1,154,014 , GRCh38.p12 chr1: 1,218,634-1,218,634 SDF4
    nsv7139601copy number variation1nstd232human GRCh37.p13 chr1: 1,161,718-1,161,779 , GRCh38.p12 chr1: 1,226,338-1,226,399 SDF4
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv7096012copy number variation1nstd102humanUncertain significance GRCh37 chr1: 980,719-1,168,648 , GRCh38.p12 chr1: 1,045,339-1,233,268 SDF4, TNFRSF18, 13 more genes
    nsv7095743copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,167,659-1,168,648 , GRCh38.p12 chr1: 1,232,279-1,233,268 B3GALT6, SDF4
    nsv7095697copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,146,935-1,168,648 , GRCh38.p12 chr1: 1,211,555-1,233,268 SDF4, TNFRSF4, 1 more genes
    nsv7044270inversion1nstd229human GRCh38 chr1: 1,133,718-2,842,494 , GRCh37.p13 chr1: 1,069,098-2,759,059 LOC105378586, MIR6726, 91 more genes
    nsv7041982inversion1nstd229human GRCh38 chr1: 1,231,599-1,288,107 , GRCh37.p13 chr1: 1,166,979-1,223,487 SCNN1D, UBE2J2, 4 more genes
    nsv6657199copy number variation1nstd229human GRCh38 chr1: 926,615-1,239,899 , GRCh37.p13 chr1: 861,995-1,175,279 TTLL10-AS1, MIR200B, 21 more genes
    nsv6641238copy number variation1nstd229human GRCh38 chr1: 1,221,271-1,221,320 , GRCh37.p13 chr1: 1,156,651-1,156,700 SDF4
    nsv6641131copy number variation1nstd229human GRCh38 chr1: 1,231,680-1,234,906 , GRCh37.p13 chr1: 1,167,060-1,170,286 SDF4, B3GALT6
    nsv6641129copy number variation1nstd229human GRCh38 chr1: 1,227,292-1,227,466 , GRCh37.p13 chr1: 1,162,672-1,162,846 SDF4
    nsv6641034copy number variation1nstd229human GRCh38 chr1: 1,232,401-1,238,600 , GRCh37.p13 chr1: 1,167,781-1,173,980 B3GALT6, SDF4
    nsv6640543copy number variation1nstd229human GRCh38 chr1: 1,156,215-1,304,768 , GRCh37.p13 chr1: 1,091,595-1,240,148 MIR429, TTLL10, 14 more genes
    nsv6640137copy number variation1nstd229human GRCh38 chr1: 1,130,518-1,270,042 , GRCh37.p13 chr1: 1,065,898-1,205,422 TTLL10, MIR429, 10 more genes
    nsv6639644copy number variation1nstd229human GRCh38 chr1: 1,089,392-1,302,400 , GRCh37.p13 chr1: 1,024,772-1,237,780 B3GALT6, C1QTNF12, 15 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6637018copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,129,319-1,264,880 , GRCh38.p12 chr1: 1,193,939-1,329,500 SNORD167, TAS1R3, 15 more genes
    nsv6636661copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,130,311-2,397,177 , GRCh38.p12 chr1: 1,194,931-2,465,738 ATAD3C, ACAP3, 69 more genes
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