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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7054932inversion1nstd229human GRCh38 chr1: 34,907,720-34,915,226 , GRCh37.p13 chr1: 35,373,321-35,380,827 DLGAP3
    nsv7053363inversion1nstd229human GRCh38 chr1: 34,907,711-34,919,853 , GRCh37.p13 chr1: 35,373,312-35,385,454 DLGAP3
    nsv7046918inversion1nstd229human GRCh38 chr1: 34,689,928-38,980,899 , GRCh37.p13 chr1: 35,155,529-39,446,571 LOC105378647, NCDN, 112 more genes
    nsv7046389inversion1nstd229human GRCh38 chr1: 31,492,639-36,569,102 , GRCh37.p13 chr1: 32,017,064-37,034,703 LOC105378642, TMEM35B, 127 more genes
    nsv6649195copy number variation1nstd229human GRCh38 chr1: 34,891,433-34,891,738 , GRCh37.p13 chr1: 35,357,034-35,357,339 DLGAP3
    nsv6649194copy number variation1nstd229human GRCh38 chr1: 34,883,658-34,884,593 , GRCh37.p13 chr1: 35,349,259-35,350,194 DLGAP3
    nsv6649193copy number variation1nstd229human GRCh38 chr1: 34,865,101-34,887,600 , GRCh37.p13 chr1: 35,330,702-35,353,201 DLGAP3
    nsv6649059copy number variation1nstd229human GRCh38 chr1: 34,896,085-34,899,026 , GRCh37.p13 chr1: 35,361,686-35,364,627 DLGAP3
    nsv6649058copy number variation1nstd229human GRCh38 chr1: 34,877,901-34,881,100 , GRCh37.p13 chr1: 35,343,502-35,346,701 DLGAP3
    nsv6636592copy number variation1nstd102humanPathogenic GRCh37 chr1: 35,104,233-37,357,913 , GRCh38.p12 chr1: 34,638,632-36,892,312 EFCAB14P1, SNORA63C, 56 more genes
    nsv6330139copy number variation1nstd223human GRCh38 chr1: 34,883,655-34,884,589 , GRCh37.p13 chr1: 35,349,256-35,350,190 DLGAP3
    nsv6322076copy number variation1nstd223human GRCh38 chr1: 34,896,076-34,899,021 , GRCh37.p13 chr1: 35,361,677-35,364,622 DLGAP3
    nsv6318349copy number variation1nstd223human GRCh38 chr1: 34,877,903-34,881,133 , GRCh37.p13 chr1: 35,343,504-35,346,734 DLGAP3
    nsv6317614copy number variation1nstd223human GRCh38 chr1: 34,559,001-35,179,400 , GRCh37.p13 chr1: 35,024,602-35,645,001 GPR199P, MIR552, 15 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6299507copy number variation1nstd186human GRCh37 chr1: 35,349,259-35,350,190 , GRCh38.p12 chr1: 34,883,658-34,884,589 DLGAP3
    nsv6242175mobile element insertion1nstd215human GRCh38 chr1: 34,865,304-34,865,304 , GRCh37.p13 chr1: 35,330,905-35,330,905 DLGAP3
    nsv6133870copy number variation1nstd213human GRCh37 chr1: 35,360,000-35,480,001 , GRCh38.p12 chr1: 34,894,399-35,014,400 ZMYM6, DLGAP3, 2 more genes
    nsv6133869copy number variation1nstd213human GRCh37 chr1: 33,400,000-36,950,001 , GRCh38.p12 chr1: 32,934,399-36,484,400 AK2, COL8A2, 77 more genes
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