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Items: 1 to 20 of 109

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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
    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
    nsv7040332inversion1nstd229human GRCh38 chr1: 34,936,903-38,057,517 , GRCh37.p13 chr1: 35,402,504-38,523,189 MAP7D1, RPL12P45, 83 more genes
    nsv6649063copy number variation1nstd229human GRCh38 chr1: 34,977,726-34,982,218 , GRCh37.p13 chr1: 35,443,327-35,447,819 GPR199P, TMEM35B
    nsv6648544copy number variation1nstd229human GRCh38 chr1: 34,984,701-34,995,800 , GRCh37.p13 chr1: 35,450,302-35,461,401 TMEM35B, ZMYM6
    nsv6648543copy number variation1nstd229human GRCh38 chr1: 34,978,642-34,980,687 , GRCh37.p13 chr1: 35,444,243-35,446,288 TMEM35B, GPR199P
    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
    nsv6331426copy number variation1nstd223human GRCh38 chr1: 34,983,936-34,993,909 , GRCh37.p13 chr1: 35,449,537-35,459,510 ZMYM6, TMEM35B
    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
    nsv6297102copy number variation1nstd186human GRCh37 chr1: 35,447,344-35,448,362 , GRCh38.p12 chr1: 34,981,743-34,982,761 TMEM35B
    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
    nsv5428972copy number variation1nstd206human GRCh38 chr1: 34,981,743-34,982,761 , GRCh37.p13 chr1: 35,447,344-35,448,362 TMEM35B
    nsv5296442copy number variation1nstd204human GRCh38.p13 chr1: 34,977,262-35,073,212 , GRCh37.p13 chr1: 35,442,863-35,538,813 ZMYM1, GPR199P, 3 more genes
    nsv5215408copy number variation1nstd204human GRCh38.p13 chr1: 34,977,101-35,073,200 , GRCh37.p13 chr1: 35,442,702-35,538,801 GPR199P, TMEM35B, 3 more genes
    nsv5212873copy number variation1nstd204human GRCh38.p13 chr1: 34,976,631-35,010,418 , GRCh37.p13 chr1: 35,442,232-35,476,019 ZMYM6, GPR199P, 1 more genes
    nsv4780772copy number variation1nstd200human GRCh37 chr1: 35,450,344-35,461,383 , GRCh38.p12 chr1: 34,984,743-34,995,782 TMEM35B, ZMYM6
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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