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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147945insertion1nstd232human GRCh37.p13 chr1: 36,068,977-36,068,977 , GRCh38.p12 chr1: 35,603,376-35,603,376 PSMB2
    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
    nsv6649449copy number variation1nstd229human GRCh38 chr1: 35,620,817-35,627,694 , GRCh37.p13 chr1: 36,086,418-36,093,295 PSMB2
    nsv6649448copy number variation1nstd229human GRCh38 chr1: 35,618,858-35,679,811 , GRCh37.p13 chr1: 36,084,459-36,145,412 LOC105378646, PSMB2
    nsv6649305copy number variation1nstd229human GRCh38 chr1: 35,615,801-35,649,700 , GRCh37.p13 chr1: 36,081,402-36,115,301 PSMB2
    nsv6649304copy number variation1nstd229human GRCh38 chr1: 35,615,654-35,618,653 , GRCh37.p13 chr1: 36,081,255-36,084,254 PSMB2
    nsv6649267copy number variation1nstd229human GRCh38 chr1: 35,616,236-35,620,473 , GRCh37.p13 chr1: 36,081,837-36,086,074 PSMB2
    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
    nsv6331690copy number variation1nstd223human GRCh38 chr1: 35,636,401-35,638,100 , GRCh37.p13 chr1: 36,102,002-36,103,701 PSMB2
    nsv6325936copy number variation1nstd223human GRCh38 chr1: 35,620,653-35,621,921 , GRCh37.p13 chr1: 36,086,254-36,087,522 PSMB2
    nsv6321842copy number variation1nstd223human GRCh38 chr1: 35,638,726-35,639,028 , GRCh37.p13 chr1: 36,104,327-36,104,629 PSMB2
    nsv6318539copy number variation1nstd223human GRCh38 chr1: 35,615,641-35,618,652 , GRCh37.p13 chr1: 36,081,242-36,084,253 PSMB2
    nsv6313765copy number variation1nstd102humanUncertain significance GRCh37 chr1: 36,041,366-39,112,237 , GRCh38.p12 chr1: 35,575,765-38,646,565 RNU6-510P, AGO3, 78 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
    nsv6313478copy number variation1nstd102humanUncertain significance GRCh37 chr1: 35,950,860-36,635,695 , GRCh38.p12 chr1: 35,485,259-36,170,094 LOC100128093, LOC105378646, 17 more genes
    nsv6150237copy number variation1nstd214human GRCh38 chr1: 35,628,578-35,628,639 , GRCh37.p13 chr1: 36,094,179-36,094,240 PSMB2
    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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