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Items: 1 to 20 of 34

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3891236copy number variation1nstd102humanBenign GRCh37 chr8: 66,738,896-66,797,059 , GRCh38.p12 chr8: 65,826,661-65,884,824 PDE7A
    nsv3907080copy number variation1nstd102humanBenign GRCh37 chr8: 66,736,695-66,782,514 , GRCh38.p12 chr8: 65,824,460-65,870,279 PDE7A
    nsv3891440copy number variation1nstd102humanBenign GRCh37 chr8: 66,738,896-66,782,514 , GRCh38.p12 chr8: 65,826,661-65,870,279 PDE7A
    nsv3894956copy number variation1nstd102humanBenign GRCh37 chr8: 66,724,605-66,760,247 , GRCh38.p12 chr8: 65,812,370-65,848,012 PDE7A
    nsv3891053copy number variation1nstd102humanBenign GRCh37 chr8: 66,736,695-66,760,247 , GRCh38.p12 chr8: 65,824,460-65,848,012 PDE7A
    nsv3903726copy number variation1nstd102humanBenign GRCh37 chr8: 66,751,871-66,760,247 , GRCh38.p12 chr8: 65,839,636-65,848,012 PDE7A
    nsv4457166copy number variation1nstd102humanUncertain significance GRCh37 chr8: 66,320,808-66,641,126 , GRCh38.p12 chr8: 65,408,573-65,728,891 PDE7A, LINC01299, 2 more genes
    nsv3905217copy number variation1nstd102humanUncertain significance GRCh37 chr8: 66,403,054-66,705,320 , GRCh38.p12 chr8: 65,490,819-65,793,085 PDE7A, ARMC1, 3 more genes
    nsv3914262copy number variation1nstd102humanPathogenic GRCh37 chr8: 63,143,195-74,140,021 , GRCh38 chr8: 62,230,636-73,227,786 , NCBI36 chr8: 63,305,749-74,302,575 PDE7A, RRS1, 151 more genes
    nsv6290731copy number variation1nstd102humanPathogenic GRCh37 chr8: 66,045,954-69,807,260 , GRCh38.p12 chr8: 65,133,719-68,895,025 PDE7A, LINC00967, 64 more genes
    nsv3891386copy number variation1nstd102humanPathogenic GRCh37 chr8: 65,194,424-68,570,319 , GRCh38.p12 chr8: 64,281,867-67,658,084 PDE7A, MTATP6P12, 66 more genes
    nsv4456190copy number variation1nstd102humanPathogenic GRCh37 chr8: 65,280,508-67,782,846 , GRCh38.p12 chr8: 64,367,951-66,870,611 PDE7A, BHLHE22-AS1, 41 more genes
    nsv3915173copy number variation1nstd102humanPathogenic NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636 PDE7A, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 PDE7A, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 PDE7A, LOC101929488, 2105 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 PDE7A, RPL5P22, 2105 more genes
    nsv3898123copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385 PDE7A, SPAG1, 2105 more genes
    nsv3908608copy number variation1nstd102humanPathogenic GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028 PDE7A, LINC01617, 2105 more genes
    nsv3893757copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442 PDE7A, LOC105375890, 2105 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 PDE7A, LOC112268023, 2105 more genes
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