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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099251copy number variation1nstd231human GRCh38.p12 chr1: 177,558,975-179,087,722 , GRCh37 chr1: 177,528,110-179,056,857 ANGPTL1, RASAL2, 24 more genes
    nsv7053017inversion1nstd229human GRCh38 chr1: 177,759,800-179,689,836 , GRCh37.p13 chr1: 177,728,935-179,658,971 LOC105371630, TEX35, 39 more genes
    nsv7050782inversion1nstd229human GRCh38 chr1: 178,302,511-179,603,198 , GRCh37.p13 chr1: 178,271,646-179,572,333 PTPN2P1, MEF2AP1, 33 more genes
    nsv7044079inversion1nstd229human GRCh38 chr1: 174,711,171-179,623,233 , GRCh37.p13 chr1: 174,680,309-179,592,368 LOC100420262, RNU6-307P, 71 more genes
    nsv6645476copy number variation1nstd229human GRCh38 chr1: 178,722,400-178,725,449 , GRCh37.p13 chr1: 178,691,535-178,694,584 RALGPS2, RALGPS2-AS1
    nsv6645473copy number variation1nstd229human GRCh38 chr1: 178,702,263-178,835,694 , GRCh37.p13 chr1: 178,671,398-178,804,829 RALGPS2, TRUND-NNN7-1, 2 more genes
    nsv6644949copy number variation1nstd229human GRCh38 chr1: 178,654,501-178,757,100 , GRCh37.p13 chr1: 178,623,636-178,726,235 PTPN2P1, RALGPS2-AS1, 3 more genes
    nsv6333146copy number variation1nstd223human GRCh38 chr1: 178,718,201-178,725,100 , GRCh37.p13 chr1: 178,687,336-178,694,235 RALGPS2, RALGPS2-AS1
    nsv6327803copy number variation1nstd223human GRCh38 chr1: 178,720,301-178,724,900 , GRCh37.p13 chr1: 178,689,436-178,694,035 RALGPS2-AS1, RALGPS2
    nsv6290451copy number variation1nstd102humanPathogenic GRCh37 chr1: 178,522,021-190,322,133 , GRCh38.p12 chr1: 178,552,886-190,353,003 RNU7-13P, LOC105371642, 167 more genes
    nsv6245871mobile element insertion1nstd215human GRCh38 chr1: 178,723,663-178,723,663 , GRCh37.p13 chr1: 178,692,798-178,692,798 RALGPS2, RALGPS2-AS1
    nsv6133950copy number variation1nstd213human GRCh37 chr1: 178,070,000-205,920,001 , GRCh38.p12 chr1: 178,100,865-205,950,873 ADORA1, CACNA1E, 442 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
    nsv6133835copy number variation1nstd213human GRCh37 chr1: 177,040,000-182,410,001 , GRCh38.p12 chr1: 177,070,864-182,440,866 VDAC1P4, RASAL2, 92 more genes
    nsv6133573copy number variation1nstd213human GRCh37 chr1: 173,820,000-189,960,001 , GRCh38.p12 chr1: 173,850,862-189,990,871 ABL2, ASTN1, 235 more genes
    nsv6115925mobile element insertion1nstd186human GRCh37 chr1: 178,692,798-178,692,849 , GRCh38.p12 chr1: 178,723,663-178,723,714 RALGPS2, RALGPS2-AS1
    nsv6056197insertion1nstd212human GRCh38 chr1: 178,723,646-178,723,646 , GRCh37.p13 chr1: 178,692,781-178,692,781 RALGPS2, RALGPS2-AS1
    nsv5964083insertion1nstd209human GRCh38 chr1: 178,723,646-178,723,646 , GRCh37.p13 chr1: 178,692,781-178,692,781 RALGPS2, RALGPS2-AS1
    nsv5828658copy number variation1nstd209human GRCh38 chr1: 178,721,986-178,753,605 , GRCh37.p13 chr1: 178,691,121-178,722,740 RALGPS2-AS1, RALGPS2, 1 more genes
    nsv5828657copy number variation1nstd209human GRCh38 chr1: 178,703,180-178,732,206 , GRCh37.p13 chr1: 178,672,315-178,701,341 RALGPS2, TRUND-NNN7-1, 1 more genes
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