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Items: 1 to 20 of 288

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7094997copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,891,090-80,333,370 , GRCh38.p12 chr17: 81,933,214-82,375,494 LOC105371939, LINC01970, 22 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6997142copy number variation1nstd229human GRCh38 chr17: 81,949,789-81,954,069 , GRCh37.p13 chr17: 79,907,665-79,911,945 NOTUM
    nsv6989489copy number variation1nstd229human GRCh38 chr17: 81,929,777-82,073,240 , GRCh37.p13 chr17: 79,887,653-80,031,116 PYCR1, ASPSCR1, 12 more genes
    nsv6988366copy number variation1nstd229human GRCh38 chr17: 81,938,036-81,951,866 , GRCh37.p13 chr17: 79,895,912-79,909,742 MYADML2, NOTUM
    nsv6525507copy number variation1nstd223human GRCh38 chr17: 81,799,201-82,693,800 , GRCh37.p13 chr17: 79,759,050-80,651,676 CENPX, RFNG, 47 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6196461copy number variation1nstd214human GRCh38 chr17: 81,952,399-81,952,450 , GRCh37.p13 chr17: 79,910,275-79,910,326 NOTUM
    nsv6146165copy number variation1nstd206human GRCh38 chr17: 81,939,133-81,955,133 , GRCh37.p13 chr17: 79,897,009-79,913,009 MYADML2, NOTUM
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
    nsv6090937insertion1nstd212human GRCh38 chr17: 81,952,370-81,952,370 , GRCh37.p13 chr17: 79,910,246-79,910,246 NOTUM
    nsv6029175copy number variation1nstd212human GRCh38 chr17: 81,952,313-81,952,402 , GRCh37.p13 chr17: 79,910,189-79,910,278 NOTUM
    nsv5978296inversion1nstd209human GRCh38 chr17: 81,945,255-82,544,213 , GRCh37.p13 chr17: 79,903,131-80,502,089 , CD7, 29 more genes
    nsv5971221insertion1nstd209human GRCh38 chr17: 81,958,593-81,958,593 , GRCh37.p13 chr17: 79,916,469-79,916,469 NOTUM
    nsv5701523mobile element insertion1nstd211human GRCh38 chr17: 81,955,345-81,955,345 , GRCh37.p13 chr17: 79,913,221-79,913,221 NOTUM
    nsv5661766insertion1nstd207human GRCh38 chr17: 81,952,348-81,952,348 , GRCh37.p13 chr17: 79,910,224-79,910,224 NOTUM
    nsv5590582copy number variation1nstd207human GRCh38 chr17: 81,952,348-81,952,415 , GRCh37.p13 chr17: 79,910,224-79,910,291 NOTUM
    nsv5556495sequence alteration1nstd206human GRCh38 chr17: 81,945,298-82,544,214 , GRCh37.p13 chr17: 79,903,174-80,502,090 , RAC3, 29 more genes
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