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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5879932copy number variation1nstd209human GRCh38 chr1: 15,436,396-15,436,624 , GRCh37.p13 chr1: 15,762,892-15,763,120 CTRC
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5417732copy number variation1nstd206human GRCh38 chr1: 15,358,943-15,442,510 , GRCh37.p13 chr1: 15,685,439-15,769,006 EFHD2, EFHD2-AS1, 2 more genes
    nsv5416270copy number variation1nstd206human GRCh38 chr1: 15,448,170-15,455,241 , GRCh37.p13 chr1: 15,774,665-15,781,736 CTRC, CELA2A
    nsv5216021copy number variation1nstd204human GRCh38.p13 chr1: 15,434,144-15,436,443 , GRCh37.p13 chr1: 15,760,640-15,762,939 CTRC
    nsv5060038copy number variation1nstd102humanUncertain significance GRCh37 chr1: 15,764,951-15,765,010 , GRCh38 chr1: 15,438,455-15,438,514 CTRC
    nsv4681335copy number variation1nstd102humanUncertain significance GRCh37 chr1: 15,764,902-15,773,084 , GRCh38.p12 chr1: 15,438,406-15,446,589 CTRC
    nsv4579753copy number variation1nstd183human GRCh37 chr1: 15,774,731-15,781,767 , GRCh38.p12 chr1: 15,448,236-15,455,272 CTRC, CELA2A
    nsv4453706copy number variation1nstd102humanUncertain significance GRCh37 chr1: 15,764,951-15,773,094 , GRCh38.p12 chr1: 15,438,455-15,446,599 CTRC
    nsv4436680complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-24,379,779 , GRCh37 chr1: 909,238-24,706,269 ALPL, RERE, 636 more genes
    nsv4436526complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-16,409,637 , GRCh37 chr1: 909,238-16,736,132 RERE, CA6, 415 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4379483copy number variation1nstd173human GRCh37 chr1: 15,756,123-15,816,655 , GRCh38.p12 chr1: 15,429,627-15,490,160 CASP9, CTRC, 4 more genes
    nsv3969248copy number variation1nstd168human GRCh38 chr1: 15,441,258-15,467,004 , GRCh37.p13 chr1: 15,767,754-15,793,499 CELA2A, CTRC, 1 more genes
    nsv3913790copy number variation1nstd102humanPathogenic NCBI36 chr1: 10,370,726-15,979,918 , GRCh37.p13 chr1: 10,448,139-16,107,331 , GRCh38.p12 chr1: 10,388,082-15,780,836 PRAMEF15, LOC105376759, 149 more genes
    nsv3912305copy number variation1nstd102humanPathogenic NCBI36 chr1: 8,912,677-16,390,632 , GRCh37.p13 chr1: 8,990,090-16,518,045 , GRCh38.p12 chr1: 8,930,031-16,191,550 DDI2, RN7SL614P, 200 more genes
    nsv3909483copy number variation1nstd102humanPathogenic NCBI36 chr1: 13,819,061-18,665,253 , GRCh38 chr1: 13,619,979-18,466,172 , GRCh37 chr1: 13,946,474-18,792,666 TMEM51, FBLIM1, 117 more genes
    nsv3908546copy number variation1nstd102humanPathogenic GRCh38 chr1: 6,554,885-16,056,011 , GRCh37 chr1: 6,614,945-16,382,506 , NCBI36 chr1: 6,537,532-16,255,093 LOC105376717, LOC107984915, 244 more genes
    nsv3906823copy number variation1nstd102humanPathogenic NCBI36 chr1: 12,707,339-16,233,870 , GRCh38 chr1: 12,724,785-16,034,788 , GRCh37 chr1: 12,784,752-16,361,283 AGMAT, HNRNPCL2, 90 more genes
    nsv3905483copy number variation1nstd102humanPathogenic GRCh38 chr1: 6,303,641-15,799,093 , NCBI36 chr1: 6,286,288-15,998,175 , GRCh37 chr1: 6,363,701-16,125,588 VPS13D, PRAMEF30P, 240 more genes
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