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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902004copy number variation1nstd209human GRCh38 chr3: 78,159,205-78,167,578 , GRCh37.p13 chr3: 78,208,356-78,216,729 RN7SKP61
    nsv5836818copy number variation1nstd209human GRCh38 chr3: 78,159,444-78,167,612 , GRCh37.p13 chr3: 78,208,595-78,216,763 RN7SKP61
    nsv5239813copy number variation1nstd204human GRCh38.p13 chr3: 78,157,001-78,160,500 , GRCh37.p13 chr3: 78,206,152-78,209,651 RN7SKP61
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 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
    nsv3922768copy number variation1nstd102humanPathogenic GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938 RNU6-557P, LOC105377160, 147 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 LOC105377187, LOC101927374, 109 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 LOC105377171, HNRNPA3P6, 323 more genes
    nsv3914429copy number variation1nstd102humanLikely benign GRCh37 chr3: 78,188,643-78,739,698 , GRCh38 chr3: 78,139,492-78,690,548 , NCBI36 chr3: 78,271,333-78,822,388 MRPS17P3, ROBO1, 1 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 RN7SKP284, OR7E121P, 122 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3881375copy number variation1nstd102humanUncertain significance GRCh37 chr3: 76,240,301-79,418,897 , GRCh38.p12 chr3: 76,191,150-79,369,747 LINC02077, RNU6-386P, 13 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3123799copy number variation1nstd151human GRCh37 chr3: 77,089,934-79,174,692 , GRCh38.p12 chr3: 77,040,783-79,125,542 MRPS17P3, VDAC1P7, 11 more genes
    nsv2767202copy number variation1nstd130human GRCh37 chr3: 77,739,202-78,451,858 , GRCh38.p12 chr3: 77,690,051-78,402,708 LOC105377173, RN7SL647P, 4 more genes
    nsv1194883copy number variation1nstd113human NCBI36 chr3: 76,485,892-79,401,678 , GRCh37.p13 chr3: 76,403,202-79,318,988 , GRCh38.p12 chr3: 76,354,051-79,269,838 , LOC102724949, 14 more genes
    nsv1190397copy number variation2nstd113human NCBI36 chr3: 77,977,982-78,391,273 , GRCh37.p13 chr3: 77,895,292-78,308,583 , GRCh38.p12 chr3: 77,846,141-78,259,433 LOC105377173, LOC105377171, 3 more genes
    nsv1188940copy number variation1nstd113human NCBI36 chr3: 67,196,224-88,524,953 , GRCh37.p13 chr3: 67,113,534-88,442,263 , GRCh38.p12 chr3: 67,063,110-88,393,113 , POU1F1, 192 more genes
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