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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138900copy number variation1nstd232human GRCh37.p13 chr1: 207,292,357-207,292,419 , GRCh38.p12 chr1: 207,119,012-207,119,074 C4BPA
    nsv7099257copy number variation1nstd231human GRCh38.p12 chr1: 203,396,218-207,103,915 , GRCh37 chr1: 203,365,346-207,277,260 ATP2B4, AVPR1B, 116 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7045682inversion1nstd229human GRCh38 chr1: 206,575,553-207,432,111 , GRCh37.p13 chr1: 206,940,870-207,605,456 CD55, RPS14P1, 26 more genes
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv7040602inversion1nstd229human GRCh38 chr1: 207,118,953-207,119,085 , GRCh37.p13 chr1: 207,292,298-207,292,430 C4BPA
    nsv6675324copy number variation1nstd229human GRCh38 chr1: 207,131,201-207,139,000 , GRCh37.p13 chr1: 207,304,546-207,312,345 C4BPA, LOC107985251
    nsv6670081copy number variation1nstd229human GRCh38 chr1: 207,142,901-207,151,600 , GRCh37.p13 chr1: 207,316,246-207,324,945 LOC107985251, C4BPA
    nsv6669278copy number variation1nstd229human GRCh38 chr1: 207,136,899-207,146,879 , GRCh37.p13 chr1: 207,310,244-207,320,224 LOC107985251, C4BPA
    nsv6666845copy number variation1nstd229human GRCh38 chr1: 207,119,018-207,119,912 , GRCh37.p13 chr1: 207,292,363-207,293,257 C4BPA
    nsv6663919copy number variation1nstd229human GRCh38 chr1: 207,143,234-207,143,276 , GRCh37.p13 chr1: 207,316,579-207,316,621 C4BPA, LOC107985251
    nsv6662459copy number variation1nstd229human GRCh38 chr1: 207,119,161-207,119,946 , GRCh37.p13 chr1: 207,292,506-207,293,291 C4BPA
    nsv6660308copy number variation1nstd229human GRCh38 chr1: 207,104,581-207,108,035 , GRCh37.p13 chr1: 207,277,926-207,281,380 C4BPA
    nsv6659335copy number variation1nstd229human GRCh38 chr1: 207,119,016-207,119,850 , GRCh37.p13 chr1: 207,292,361-207,293,195 C4BPA
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6554793inversion1nstd223human GRCh38 chr1: 207,105,279-207,106,736 , GRCh37.p13 chr1: 207,278,624-207,280,081 C4BPA
    nsv6554773inversion1nstd223human GRCh38 chr1: 204,500,842-208,290,127 , GRCh37.p13 chr1: 204,469,970-208,463,472 RNA5SP75, LOC105372869, 108 more genes
    nsv6549747inversion1nstd223human GRCh38 chr1: 207,118,922-207,119,083 , GRCh37.p13 chr1: 207,292,267-207,292,428 C4BPA
    nsv6545599inversion1nstd223human GRCh38 chr1: 207,135,065-207,137,632 , GRCh37.p13 chr1: 207,308,410-207,310,977 C4BPA, LOC107985251
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