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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883359copy number variation1nstd102humanBenign GRCh37 chr3: 89,379,935-89,440,509 , GRCh38.p12 chr3: 89,330,785-89,391,359 EPHA3
    nsv3879218copy number variation1nstd102humanBenign GRCh37 chr3: 89,384,566-89,440,509 , GRCh38.p12 chr3: 89,335,416-89,391,359 EPHA3
    nsv3887669copy number variation1nstd102humanBenign GRCh37 chr3: 89,150,942-89,379,935 , GRCh38.p12 chr3: 89,101,792-89,330,785 EPHA3
    nsv3884448copy number variation2nstd102humannot provided GRCh38 chr3: 89,335,416-89,368,021 , GRCh37 chr3: 89,384,566-89,417,171 EPHA3
    nsv3888652copy number variation1nstd102humanUncertain significance GRCh37 chr3: 89,381,249-89,529,462 , GRCh38.p12 chr3: 89,332,099-89,480,312 EPHA3
    esv3648993copy number variation1estd216humannot provided GRCh37 chr3: 89,384,566-89,417,171 , GRCh38.p12 chr3: 89,335,416-89,368,021 EPHA3
    esv3648117copy number variation1estd216humannot provided GRCh37 chr3: 89,384,566-89,417,171 , GRCh38.p12 chr3: 89,335,416-89,368,021 EPHA3
    nsv3876149copy number variation1nstd102humanBenign GRCh37 chr3: 89,417,287-89,686,064 , GRCh38.p12 chr3: 89,368,137-89,636,914 EPHA3, MTATP6P6, 3 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 EPHA3, LOC105377171, 323 more genes
    nsv3911768copy number variation1nstd102humanPathogenic NCBI36 chr3: 73,956,712-90,585,539 , GRCh37 chr3: 73,874,022-90,502,849 , GRCh38 chr3: 73,824,871-90,453,699 EPHA3, RN7SKP284, 122 more genes
    nsv3916669copy number variation1nstd102humanPathogenic NCBI36 chr3: 74,781,223-89,627,521 , GRCh37 chr3: 74,698,533-89,544,831 , GRCh38 chr3: 74,649,382-89,495,681 EPHA3, LOC105377187, 109 more genes
    nsv3912034copy number variation1nstd102humanPathogenic GRCh38 chr3: 82,912,987-90,179,222 , GRCh37 chr3: 82,962,138-90,228,372 , NCBI36 chr3: 83,044,828-90,311,062 EPHA3, MTATP6P6, 49 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 EPHA3, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 EPHA3, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 EPHA3, RPL23AP49, 2875 more genes
    nsv3923231copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 76,896,101-89,814,775 , GRCh37 chr3: 76,813,411-89,732,085 , GRCh38 chr3: 76,764,260-89,682,935 EPHA3, GBE1, 80 more genes
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 EPHA3, AKR1B1P2, 231 more genes
    nsv3874413copy number variation1nstd102humanBenign GRCh37 chr3: 89,440,509-90,504,539 , GRCh38.p12 chr3: 89,391,359-90,455,389 EPHA3, HSPE1P19, 6 more genes
    nsv6291230copy number variation1nstd102humanUncertain significance GRCh37 chr3: 88,159,133-90,502,849 , GRCh38.p12 chr3: 88,109,983-90,453,699 EPHA3, RNU6-712P, 15 more genes
    nsv4674450copy number variation1nstd102humanUncertain significance GRCh37 chr3: 89,369,130-90,485,949 , GRCh38.p12 chr3: 89,319,980-90,436,799 EPHA3, MTCO2P6, 6 more genes
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