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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923719copy number variation1nstd209human GRCh38 chr10: 74,029,071-74,029,364 , GRCh37.p13 chr10: 75,788,829-75,789,122 VCL
    nsv5919916copy number variation1nstd209human GRCh38 chr10: 74,105,861-74,105,915 , GRCh37.p13 chr10: 75,865,619-75,865,673 VCL
    nsv5910319copy number variation1nstd209human GRCh38 chr10: 74,099,318-74,099,894 , GRCh37.p13 chr10: 75,859,076-75,859,652 VCL
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5697167mobile element insertion1nstd211human GRCh38 chr10: 74,069,990-74,069,990 , GRCh37.p13 chr10: 75,829,748-75,829,748 VCL
    nsv5696591mobile element insertion1nstd211human GRCh38 chr10: 74,090,302-74,090,302 , GRCh37.p13 chr10: 75,850,060-75,850,060 , VCL
    nsv5628108insertion1nstd207human GRCh38 chr10: 74,105,913-74,105,913 , GRCh37.p13 chr10: 75,865,671-75,865,671 VCL
    nsv5564206copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,863,568-75,865,121 , GRCh38.p12 chr10: 74,103,810-74,105,363 VCL
    nsv5491364copy number variation1nstd206human GRCh38 chr10: 74,009,492-74,009,903 , GRCh37.p13 chr10: 75,769,250-75,769,661 VCL
    nsv5486195copy number variation1nstd206human GRCh38 chr10: 74,062,444-74,063,096 , GRCh37.p13 chr10: 75,822,202-75,822,854 VCL
    nsv5481105copy number variation1nstd206human GRCh38 chr10: 74,099,298-74,099,917 , GRCh37.p13 chr10: 75,859,056-75,859,675 VCL
    nsv5480551copy number variation1nstd206human GRCh38 chr10: 74,117,605-74,117,660 , GRCh37.p13 chr10: 75,877,363-75,877,418 VCL
    nsv5480136copy number variation1nstd206human GRCh38 chr10: 74,106,012-74,106,115 , GRCh37.p13 chr10: 75,865,770-75,865,873 VCL
    nsv5347857translocation1nstd200human GRCh38 chr10: 74,117,660-74,117,660 , GRCh38 chr10: 74,117,605-74,117,605 , GRCh37.p13 chr10: 75,877,418-75,877,418 , GRCh37.p13 chr10: 75,877,363-75,877,363 VCL
    nsv5313565copy number variation1nstd204human GRCh38.p13 chr10: 74,099,308-74,099,902 , GRCh37.p13 chr10: 75,859,066-75,859,660 VCL
    nsv5301974copy number variation1nstd204human GRCh38.p13 chr10: 73,709,242-74,768,785 , GRCh37.p13 chr10: 75,469,000-76,528,543 , RPSAP6, 24 more genes
    nsv5248555copy number variation1nstd204human GRCh38.p13 chr10: 74,039,476-74,075,378 , GRCh37.p13 chr10: 75,799,234-75,835,136 , VCL
    nsv5248085copy number variation1nstd204human GRCh38.p13 chr10: 74,116,618-74,196,286 , GRCh37.p13 chr10: 75,876,376-75,956,044 VCL, ADK, 1 more genes
    nsv5131288mobile element insertion1nstd203human GRCh38 chr10: 74,069,981-74,069,990 , GRCh37.p13 chr10: 75,829,739-75,829,748 VCL
    nsv5127434mobile element insertion1nstd203human GRCh38 chr10: 74,017,046-74,017,065 , GRCh37.p13 chr10: 75,776,804-75,776,823 VCL
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