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Items: 18

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    Number of Variants: 18

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3920790copy number variation1nstd102humanPathogenic GRCh38 chr3: 134,257,180-149,729,538 , NCBI36 chr3: 135,458,712-150,930,015 , GRCh37 chr3: 133,976,022-149,447,325 TRPC1, TFDP2, 203 more genes
    nsv3920279copy number variation1nstd102humanPathogenic GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156 TRPC1, NPHP3-AS1, 218 more genes
    nsv3921297copy number variation1nstd102humanPathogenic NCBI36 chr3: 133,918,512-145,986,275 , GRCh38 chr3: 132,716,978-144,784,743 , GRCh37 chr3: 132,435,822-144,503,585 TRPC1, BFSP2, 169 more genes
    nsv3921636copy number variation1nstd102humanPathogenic GRCh38 chr3: 135,227,451-145,870,770 , NCBI36 chr3: 136,428,983-147,071,247 , GRCh37 chr3: 134,946,293-145,588,557 TRPC1, A4GNT, 134 more genes
    nsv3923685copy number variation1nstd102humanPathogenic GRCh37 chr3: 137,650,842-144,187,581 , NCBI36 chr3: 139,133,532-145,670,271 , GRCh38 chr3: 137,932,000-144,468,739 TRPC1, ATP1B3, 97 more genes
    nsv3910200copy number variation1nstd102humanPathogenic GRCh38 chr3: 141,751,960-148,246,189 , GRCh37 chr3: 141,470,802-147,963,976 , NCBI36 chr3: 142,953,492-149,446,666 TRPC1, LNCSRLR, 70 more genes
    nsv3915603copy number variation1nstd102humanPathogenic NCBI36 chr3: 139,192,655-144,820,318 , GRCh38 chr3: 137,991,123-143,618,786 , GRCh37 chr3: 137,709,965-143,337,628 TRPC1, NME9, 91 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 TRPC1, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 TRPC1, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 TRPC1, RPL23AP49, 2875 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 TRPC1, LINC02614, 1469 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 TRPC1, H1-10, 846 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 TRPC1, OR7E53P, 794 more genes
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 TRPC1, MBNL1-AS1, 339 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 TRPC1, MTAPP1, 339 more genes
    nsv4347615copy number variation1nstd102humanPathogenic GRCh37 chr3: 135,288,025-146,874,012 , GRCh38.p12 chr3: 135,569,183-147,156,225 TRPC1, RPL6P9, 145 more genes
    nsv3916859copy number variation1nstd102humanUncertain significance GRCh37 chr3: 142,499,640-145,951,714 , NCBI36 chr3: 143,982,330-147,434,404 , GRCh38 chr3: 142,780,798-146,233,927 TRPC1, LARP7P4, 33 more genes
    nsv3877516copy number variation1nstd102humanUncertain significance GRCh37 chr3: 142,272,098-142,691,972 , GRCh38.p12 chr3: 142,553,256-142,973,130 TRPC1, PLS1-AS1, 11 more genes
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