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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072039inversion1nstd229human GRCh38 chr16: 79,903,600-82,537,648 , GRCh37.p13 chr16: 79,937,497-82,571,253 RN7SKP176, LOC105371357, 34 more genes
    nsv7070808inversion1nstd229human GRCh38 chr16: 79,903,594-82,532,651 , GRCh37.p13 chr16: 79,937,491-82,566,256 DYNLRB2, RNU6-1191P, 34 more genes
    nsv7069467inversion1nstd229human GRCh38 chr16: 77,603,047-81,438,175 , GRCh37.p13 chr16: 77,636,944-81,471,780 ATMIN, WWOX, 39 more genes
    nsv6996325copy number variation1nstd229human GRCh38 chr16: 80,515,024-80,544,254 , GRCh37.p13 chr16: 80,548,921-80,578,151 DYNLRB2-AS1, DYNLRB2
    nsv6995966copy number variation1nstd229human GRCh38 chr16: 80,497,813-80,587,021 , GRCh37.p13 chr16: 80,531,710-80,620,918 DYNLRB2, LINC01227, 1 more genes
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6993656copy number variation1nstd229human GRCh38 chr16: 80,348,419-81,288,034 , GRCh37.p13 chr16: 80,382,316-81,321,639 BCO1, RNU6-1191P, 13 more genes
    nsv6983964copy number variation1nstd229human GRCh38 chr16: 80,542,988-80,577,040 , GRCh37.p13 chr16: 80,576,885-80,610,937 DYNLRB2-AS1, LINC01227, 1 more genes
    nsv6982947copy number variation1nstd229human GRCh38 chr16: 80,539,080-80,545,366 , GRCh37.p13 chr16: 80,572,977-80,579,263 DYNLRB2, DYNLRB2-AS1
    nsv6981613copy number variation1nstd229human GRCh38 chr16: 80,536,147-80,538,597 , GRCh37.p13 chr16: 80,570,044-80,572,494 DYNLRB2, DYNLRB2-AS1
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6511919copy number variation1nstd223human GRCh38 chr16: 80,354,904-80,551,922 , GRCh37.p13 chr16: 80,388,801-80,585,819 DYNLRB2-AS1, DYNLRB2
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6314107copy number variation1nstd102humanUncertain significance GRCh37 chr16: 77,960,664-81,429,258 , GRCh38.p12 chr16: 77,926,767-81,395,653 ARLNC1, MAF, 36 more genes
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
    nsv6133211copy number variation1nstd213human GRCh37 chr16: 79,110,000-80,850,001 , GRCh38.p12 chr16: 79,076,103-80,816,104 MAF, WWOX, 12 more genes
    nsv6133210copy number variation1nstd213human GRCh37 chr16: 78,970,000-88,180,001 , GRCh38.p12 chr16: 78,936,103-88,146,395 , CA5A, 152 more genes
    nsv6133206copy number variation1nstd213human GRCh37 chr16: 74,460,000-84,740,001 , GRCh38.p12 chr16: 74,426,102-84,706,395 , CDH13, 142 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6103932inversion1nstd212human GRCh38 chr16: 80,118,640-80,990,819 , GRCh37.p13 chr16: 80,152,537-81,024,424 , CMC2, 6 more genes
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