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Items: 1 to 20 of 1804

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3881933copy number variation1nstd102humanPathogenic GRCh38 chr3: 70,992,485-71,180,270 , GRCh37 chr3: 71,041,636-71,229,421 FOXP1
    nsv4674612copy number variation1nstd102humanPathogenic GRCh37 chr3: 71,081,905-71,227,572 , GRCh38.p12 chr3: 71,032,754-71,178,421 FOXP1
    nsv6313809copy number variation1nstd102humanPathogenic GRCh37 chr3: 71,251,088-71,312,384 , GRCh38.p12 chr3: 71,201,937-71,263,233 FOXP1
    nsv3871884copy number variation1nstd102humanPathogenic GRCh37 chr3: 71,008,556-71,049,017 , GRCh38.p12 chr3: 70,959,405-70,999,866 FOXP1
    nsv3871791copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 71,129,956-71,255,015 , GRCh38.p12 chr3: 71,080,805-71,205,864 FOXP1
    nsv3889046copy number variation1nstd102humanBenign GRCh37 chr3: 71,631,606-71,652,888 , GRCh38.p12 chr3: 71,582,455-71,603,737 FOXP1
    nsv3874008copy number variation1nstd102humanBenign GRCh37 chr3: 71,383,767-71,397,385 , GRCh38.p12 chr3: 71,334,616-71,348,234 FOXP1
    nsv3910965copy number variation1nstd102humanLikely benign GRCh37 chr3: 71,152,133-71,210,298 , GRCh38 chr3: 71,102,982-71,161,147 , NCBI36 chr3: 71,234,823-71,292,988 FOXP1
    nsv3876348copy number variation1nstd102humanBenign GRCh37 chr3: 71,505,403-71,509,083 , GRCh38.p12 chr3: 71,456,252-71,459,932 FOXP1
    nsv7098863copy number variation1nstd102humannot provided GRCh37 chr3: 71,021,211-71,181,046 , GRCh38.p12 chr3: 70,972,060-71,131,895 FOXP1
    nsv3882938copy number variation1nstd102humanUncertain significance GRCh37 chr3: 71,363,860-71,500,334 , GRCh38.p12 chr3: 71,314,709-71,451,183 FOXP1
    esv4009671copy number variation1estd231human GRCh37 chr3: 71,242,337-71,242,638 , GRCh38.p12 chr3: 71,193,186-71,193,487 FOXP1
    nsv4578368copy number variation1nstd102humanUncertain significance GRCh37 chr3: 71,161,687-71,247,532 , GRCh38.p12 chr3: 71,112,536-71,198,381 FOXP1
    nsv6705186copy number variation1nstd229human GRCh38 chr3: 71,168,201-71,215,700 , GRCh37.p13 chr3: 71,217,352-71,264,851 FOXP1
    nsv6701023copy number variation1nstd229human GRCh38 chr3: 71,390,546-71,407,873 , GRCh37.p13 chr3: 71,439,697-71,457,024 FOXP1
    nsv6703953copy number variation1nstd229human GRCh38 chr3: 71,313,154-71,324,233 , GRCh37.p13 chr3: 71,362,305-71,373,384 FOXP1
    nsv6713217copy number variation1nstd229human GRCh38 chr3: 71,469,828-71,476,871 , GRCh37.p13 chr3: 71,518,979-71,526,022 FOXP1
    nsv6709679copy number variation1nstd229human GRCh38 chr3: 71,091,658-71,098,077 , GRCh37.p13 chr3: 71,140,809-71,147,228 FOXP1
    nsv6715402copy number variation1nstd229human GRCh38 chr3: 71,487,426-71,493,138 , GRCh37.p13 chr3: 71,536,577-71,542,289 FOXP1
    nsv6704187copy number variation1nstd229human GRCh38 chr3: 71,431,801-71,437,461 , GRCh37.p13 chr3: 71,480,952-71,486,612 FOXP1
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