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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099021copy number variation1nstd102humanPathogenic GRCh38 chr13: 20,222,821-20,531,941 , GRCh37.p13 chr13: 20,796,960-21,106,080 MIR4499, LOC105370102, 2 more genes
    nsv7094395copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,797,176-21,105,944 , GRCh38.p12 chr13: 20,223,037-20,531,805 MIR4499, LOC105370102, 2 more genes
    nsv7093992copy number variation1nstd102humanUncertain significance GRCh37 chr13: 20,796,834-21,099,933 , GRCh38.p12 chr13: 20,222,695-20,525,794 CRYL1, GJB6, 2 more genes
    nsv7093991copy number variation2nstd102humanUncertain significance GRCh37 chr13: 20,763,040-20,797,619 , GRCh38.p12 chr13: 20,188,901-20,223,480 GJB2, GJB6
    nsv7073674inversion1nstd229human GRCh38 chr13: 19,051,673-20,424,293 , GRCh37.p13 chr13: 19,625,813-20,998,432 ST6GALNAC4P1, LINC01072, 35 more genes
    nsv7073256inversion1nstd229human GRCh38 chr13: 19,714,497-24,851,015 , GRCh37.p13 chr13: 20,288,637-25,425,153 SPATA13, IFT88, 114 more genes
    nsv7072424inversion1nstd229human GRCh38 chr13: 20,061,787-21,405,901 , GRCh37.p13 chr13: 20,635,927-21,980,040 IPPKP1, CRYL1, 41 more genes
    nsv7071368inversion1nstd229human GRCh38 chr13: 19,560,696-21,260,853 , GRCh37.p13 chr13: 20,134,836-21,834,992 ZMYM2, EEF1AKMT1, 44 more genes
    nsv7071034inversion1nstd229human GRCh38 chr13: 19,239,514-24,381,508 , GRCh37.p13 chr13: 19,813,654-24,955,646 BASP1P1, ZMYM5, 111 more genes
    nsv7067925inversion1nstd229human GRCh38 chr13: 19,527,899-24,671,591 , GRCh37.p13 chr13: 20,102,039-25,245,729 TPTE2-AS1, TNFRSF19, 112 more genes
    nsv7067291inversion1nstd229human GRCh38 chr13: 20,213,107-20,285,066 , GRCh37.p13 chr13: 20,787,246-20,859,205 GJB6
    nsv7065933inversion1nstd229human GRCh38 chr13: 19,560,717-21,260,795 , GRCh37.p13 chr13: 20,134,857-21,834,934 LOC105370101, GJB2, 44 more genes
    nsv7060563inversion1nstd229human GRCh38 chr13: 20,114,084-20,492,768 , GRCh37.p13 chr13: 20,688,223-21,066,907 LOC105370101, GJA3, 7 more genes
    nsv7058292inversion1nstd229human GRCh38 chr13: 19,736,413-23,270,103 , GRCh37.p13 chr13: 20,310,553-23,844,242 PPIAP28, RPL7AP73, 75 more genes
    nsv6938034copy number variation1nstd229human GRCh38 chr13: 20,228,605-20,229,153 , GRCh37.p13 chr13: 20,802,744-20,803,292 GJB6
    nsv6933609copy number variation1nstd229human GRCh38 chr13: 20,211,901-20,251,800 , GRCh37.p13 chr13: 20,786,040-20,825,939 GJB6
    nsv6932865copy number variation1nstd229human GRCh38 chr13: 20,217,021-20,228,749 , GRCh37.p13 chr13: 20,791,160-20,802,888 GJB6
    nsv6932713copy number variation1nstd229human GRCh38 chr13: 19,442,684-24,587,300 , GRCh37.p13 chr13: 20,016,824-25,161,438 CEND1P2, MTCO3P2, 112 more genes
    nsv6931978copy number variation1nstd229human GRCh38 chr13: 20,230,700-20,489,184 , GRCh37.p13 chr13: 20,804,839-21,063,323 CRYL1, GJB6, 2 more genes
    nsv6931948copy number variation1nstd229human GRCh38 chr13: 20,228,607-20,460,609 , GRCh37.p13 chr13: 20,802,746-21,034,748 LOC105370102, CRYL1, 2 more genes
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