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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099254copy number variation1nstd231human GRCh38.p12 chr1: 182,376,401-191,898,122 , GRCh37 chr1: 182,345,536-191,867,252 DHX9, GLUL, 99 more genes
    nsv7056023inversion1nstd229human GRCh38 chr1: 185,100,692-185,100,745 , GRCh37.p13 chr1: 185,069,824-185,069,877 RNF2
    nsv7053326inversion1nstd229human GRCh38 chr1: 183,856,809-187,909,288 , GRCh37.p13 chr1: 183,825,943-187,878,419 RGL1, TPR, 49 more genes
    nsv6646333copy number variation1nstd229human GRCh38 chr1: 185,064,272-185,073,476 , GRCh37.p13 chr1: 185,033,404-185,042,608 FTH1P25, RNF2
    nsv6646254copy number variation1nstd229human GRCh38 chr1: 185,063,446-185,063,632 , GRCh37.p13 chr1: 185,032,578-185,032,764 RNF2
    nsv6646181copy number variation1nstd229human GRCh38 chr1: 185,077,155-185,077,627 , GRCh37.p13 chr1: 185,046,287-185,046,759 RNF2
    nsv6645818copy number variation1nstd229human GRCh38 chr1: 185,054,427-185,054,505 , GRCh37.p13 chr1: 185,023,559-185,023,637 RNF2
    nsv6645817copy number variation1nstd229human GRCh38 chr1: 185,052,816-185,062,175 , GRCh37.p13 chr1: 185,021,948-185,031,307 RNF2
    nsv6637124copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,727,182-192,260,142 , GRCh38.p12 chr1: 179,758,047-192,291,012 LOC101928933, KIAA1614-AS1, 148 more genes
    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
    nsv6548934inversion1nstd223human GRCh38 chr1: 183,856,809-187,909,292 , GRCh37.p13 chr1: 183,825,943-187,878,423 LOC105371649, LINC01633, 49 more genes
    nsv6332101copy number variation1nstd223human GRCh38 chr1: 185,005,242-185,044,832 , GRCh37.p13 chr1: 184,974,374-185,013,964 LINC01633, RNF2, 1 more genes
    nsv6332066copy number variation1nstd223human GRCh38 chr1: 185,064,272-185,073,474 , GRCh37.p13 chr1: 185,033,404-185,042,606 FTH1P25, RNF2
    nsv6325313copy number variation1nstd223human GRCh38 chr1: 185,042,601-185,047,200 , GRCh37.p13 chr1: 185,011,733-185,016,332 RNF2
    nsv6321193copy number variation1nstd223human GRCh38 chr1: 185,077,249-185,077,559 , GRCh37.p13 chr1: 185,046,381-185,046,691 RNF2
    nsv6316476copy number variation1nstd223human GRCh38 chr1: 184,855,810-185,076,387 , GRCh37.p13 chr1: 184,824,944-185,045,519 RNF2, NIBAN1, 3 more genes
    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
    nsv6133952copy number variation1nstd213human GRCh37 chr1: 182,620,000-185,630,001 , GRCh38.p12 chr1: 182,650,865-185,660,869 DHX9, IVNS1ABP, 54 more genes
    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
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