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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099255copy number variation1nstd231human GRCh38.p12 chr1: 192,358,641-201,911,882 , GRCh37 chr1: 192,327,771-201,881,010 CACNA1S, CSRP1, 120 more genes
    nsv7057871inversion1nstd229human GRCh38 chr1: 191,728,426-196,575,913 , GRCh37.p13 chr1: 191,697,556-196,545,043 GLRX2, LOC107985241, 37 more genes
    nsv7044147inversion1nstd229human GRCh38 chr1: 190,518,287-195,020,156 , GRCh37.p13 chr1: 190,487,417-194,989,286 LOC105371668, B3GALT2, 34 more genes
    nsv6673597copy number variation1nstd229human GRCh38 chr1: 192,803,180-193,399,191 , GRCh37.p13 chr1: 192,772,310-193,368,321 RO60, MIR1278, 12 more genes
    nsv6672020copy number variation1nstd229human GRCh38 chr1: 192,852,092-192,877,616 , GRCh37.p13 chr1: 192,821,222-192,846,746 LOC105371668, RN7SKP126, 1 more genes
    nsv6671987copy number variation1nstd229human GRCh38 chr1: 192,872,258-192,886,368 , GRCh37.p13 chr1: 192,841,388-192,855,498 RN7SKP126
    nsv6667360copy number variation1nstd229human GRCh38 chr1: 192,840,479-192,969,206 , GRCh37.p13 chr1: 192,809,609-192,938,336 RN7SKP126, RGS2-AS1, 2 more genes
    nsv6664098copy number variation1nstd229human GRCh38 chr1: 189,813,413-194,218,341 , GRCh37.p13 chr1: 189,782,543-194,187,471 RO60, MIR4426, 38 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
    nsv6636659copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 189,633,885-199,854,163 , GRCh38.p12 chr1: 189,664,755-199,885,035 F13B, CFH, 88 more genes
    nsv6540558inversion1nstd223human GRCh38 chr1: 192,830,119-193,074,178 , GRCh37.p13 chr1: 192,799,249-193,043,308 RO60, UCHL5, 6 more genes
    nsv6325959copy number variation1nstd223human GRCh38 chr1: 192,857,716-192,896,746 , GRCh37.p13 chr1: 192,826,846-192,865,876 LOC105371668, RN7SKP126
    nsv6313702copy number variation1nstd102humanUncertain significance GRCh37 chr1: 192,731,793-193,391,298 , GRCh38.p12 chr1: 192,762,663-193,422,168 RO60, SCARNA18B, 14 more genes
    nsv6133957copy number variation1nstd213human GRCh37 chr1: 192,200,000-199,690,001 , GRCh38.p12 chr1: 192,230,870-199,720,873 PTPRC, RGS2, 73 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
    nsv6133611copy number variation1nstd213human GRCh37 chr1: 191,020,000-199,730,001 , GRCh38.p12 chr1: 191,050,870-199,760,873 F13B, CFH, 79 more genes
    nsv5973567inversion1nstd209human GRCh38 chr1: 192,830,119-193,074,177 , GRCh37.p13 chr1: 192,799,249-193,043,307 RO60, UCHL5, 6 more genes
    nsv5887494copy number variation1nstd209human GRCh38 chr1: 192,263,809-193,558,335 , GRCh37.p13 chr1: 192,232,939-193,527,465 , LINC01031, 22 more genes
    nsv5869797copy number variation1nstd209human GRCh38 chr1: 192,820,803-192,881,097 , GRCh37.p13 chr1: 192,789,933-192,850,227 LOC105371667, LOC105371668, 1 more genes
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