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Items: 1 to 20 of 605

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6311558copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,872,031-227,985,874 , GRCh38.p12 chr2: 227,007,315-227,121,158 COL4A4
    nsv7096612copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,892,598-227,974,022 , GRCh38.p12 chr2: 227,027,882-227,109,306 COL4A4
    nsv4347134copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,939,002-227,943,108 , GRCh38.p12 chr2: 227,074,286-227,078,392 COL4A4
    nsv7096614copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,963,400-227,966,635 , GRCh38.p12 chr2: 227,098,684-227,101,919 COL4A4
    nsv4674237copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,942,610-227,945,265 , GRCh38.p12 chr2: 227,077,894-227,080,549 COL4A4
    nsv7096140copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,914,764-227,917,148 , GRCh38.p12 chr2: 227,050,048-227,052,432 COL4A4
    nsv7096403copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,872,031-227,873,030 , GRCh38.p12 chr2: 227,007,315-227,008,314 COL4A4
    nsv6311379copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,872,041-227,872,324 , GRCh38.p12 chr2: 227,007,325-227,007,608 COL4A4
    nsv7096613copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,946,821-227,946,913 , GRCh38.p12 chr2: 227,082,105-227,082,197 COL4A4
    nsv4683296copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,012,119-228,012,209 , GRCh38.p12 chr2: 227,147,403-227,147,493 COL4A4
    nsv1397984copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,958,838-227,958,889 , GRCh38 chr2: 227,094,122-227,094,173 COL4A4
    nsv6311643copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 227,945,139-227,976,449 , GRCh38.p12 chr2: 227,080,423-227,111,733 COL4A4
    nsv6311380copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 227,917,001-227,924,979 , GRCh38.p12 chr2: 227,052,285-227,060,263 COL4A4
    nsv6311642copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 227,922,145-227,927,324 , GRCh38.p12 chr2: 227,057,429-227,062,608 COL4A4
    nsv6311644copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 227,973,277-227,974,022 , GRCh38.p12 chr2: 227,108,561-227,109,306 COL4A4
    nsv5673534copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 227,946,821-227,964,415 , GRCh38.p12 chr2: 227,082,105-227,099,699 COL4A4
    nsv3880090copy number variation1nstd102humanBenign GRCh37 chr2: 227,892,619-227,912,237 , GRCh38.p12 chr2: 227,027,903-227,047,521 COL4A4
    nsv3873215copy number variation1nstd102humanBenign GRCh37 chr2: 227,892,658-227,912,247 , GRCh38.p12 chr2: 227,027,942-227,047,531 COL4A4
    nsv3874404copy number variation1nstd102humanBenign GRCh37 chr2: 227,892,619-227,912,144 , GRCh38.p12 chr2: 227,027,903-227,047,428 COL4A4
    nsv3881348copy number variation1nstd102humanBenign GRCh37 chr2: 227,911,037-227,912,247 , GRCh38.p12 chr2: 227,046,321-227,047,531 COL4A4
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