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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096542copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,876,443-148,885,037 , GRCh38.p12 chr3: 149,158,656-149,167,250 CP, HPS3
    nsv7049472inversion1nstd229human GRCh38 chr3: 149,203,819-149,207,836 , GRCh37.p13 chr3: 148,921,606-148,925,623 CP
    nsv6736660copy number variation1nstd229human GRCh38 chr3: 149,137,977-149,417,965 , GRCh37.p13 chr3: 148,855,764-149,135,752 , TM4SF18, 8 more genes
    nsv6734774copy number variation1nstd229human GRCh38 chr3: 149,181,975-149,195,539 , GRCh37.p13 chr3: 148,899,762-148,913,326 CP
    nsv6734453copy number variation1nstd229human GRCh38 chr3: 149,201,367-149,201,683 , GRCh37.p13 chr3: 148,919,154-148,919,470 CP
    nsv6734085copy number variation1nstd229human GRCh38 chr3: 149,108,152-149,204,911 , GRCh37.p13 chr3: 148,825,939-148,922,698 HPS3, CP
    nsv6733956copy number variation1nstd229human GRCh38 chr3: 149,213,147-149,216,183 , GRCh37.p13 chr3: 148,930,934-148,933,970 CP
    nsv6728442copy number variation1nstd229human GRCh38 chr3: 149,162,782-149,166,990 , GRCh37.p13 chr3: 148,880,569-148,884,777 CP, HPS3
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6566521inversion1nstd223human GRCh38 chr3: 149,171,173-149,171,755 , GRCh37.p13 chr3: 148,888,960-148,889,542 HPS3, CP
    nsv6372439copy number variation1nstd223human GRCh38 chr3: 149,209,712-149,210,265 , GRCh37.p13 chr3: 148,927,499-148,928,052 CP
    nsv6366462copy number variation1nstd223human GRCh38 chr3: 149,167,501-149,168,500 , GRCh37.p13 chr3: 148,885,288-148,886,287 HPS3, CP
    nsv6315250copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 148,890,285-148,939,833 , GRCh38.p12 chr3: 149,172,498-149,222,046 CP, HPS3
    nsv6315216copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 148,847,728-148,890,984 , GRCh38.p12 chr3: 149,129,941-149,173,197 CP, HPS3
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6311445copy number variation1nstd102humanUncertain significance GRCh37 chr3: 148,847,511-148,906,009 , GRCh38.p12 chr3: 149,129,724-149,188,222 CP, HPS3
    nsv6311444copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709 TM4SF1, FKBP1AP4, 68 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134994copy number variation1nstd213human GRCh37 chr3: 139,490,000-150,360,001 , GRCh38.p12 chr3: 139,771,158-150,642,214 , ATP1B3, 147 more genes
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