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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148127copy number variation1nstd102humanUncertain significance GRCh37 chr7: 10,973,263-14,669,896 , GRCh38.p12 chr7: 10,933,636-14,630,271 LOC105375162, LOC105375156, 33 more genes
    nsv7054063inversion1nstd229human GRCh38 chr7: 7,723,636-12,911,662 , GRCh37.p13 chr7: 7,763,267-12,951,287 NXPH1, CCNB2P1, 50 more genes
    nsv7040359inversion1nstd229human GRCh38 chr7: 10,934,266-10,934,299 , GRCh37.p13 chr7: 10,973,893-10,973,926 NDUFA4
    nsv6817374copy number variation1nstd229human GRCh38 chr7: 10,753,988-11,038,567 , GRCh37.p13 chr7: 10,793,615-11,078,194 PHF14, MGC4859, 3 more genes
    nsv6815656copy number variation1nstd229human GRCh38 chr7: 10,923,832-10,930,324 , GRCh37.p13 chr7: 10,963,459-10,969,951 NDUFA4
    nsv6814186copy number variation1nstd229human GRCh38 chr7: 10,823,305-11,529,482 , GRCh37.p13 chr7: 10,862,932-11,569,109 PHF14, THSD7A, 4 more genes
    nsv6808151copy number variation1nstd229human GRCh38 chr7: 10,838,211-11,332,367 , GRCh37.p13 chr7: 10,877,838-11,371,994 RPL23AP52, LOC107986767, 3 more genes
    nsv6807019copy number variation1nstd229human GRCh38 chr7: 10,525,147-10,994,926 , GRCh37.p13 chr7: 10,564,774-11,034,553 LOC107986766, LOC107986767, 4 more genes
    nsv6804070copy number variation1nstd229human GRCh38 chr7: 10,937,936-10,987,218 , GRCh37.p13 chr7: 10,977,563-11,026,845 NDUFA4, LOC107986767, 1 more genes
    nsv6801177copy number variation1nstd229human GRCh38 chr7: 10,814,397-11,282,510 , GRCh37.p13 chr7: 10,854,024-11,322,137 RPL23AP52, LOC107986767, 3 more genes
    nsv6800441copy number variation1nstd229human GRCh38 chr7: 10,592,949-11,345,993 , GRCh37.p13 chr7: 10,632,576-11,385,620 NDUFA4, RPL23AP52, 6 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632271copy number variation1nstd224human GRCh37 chr7: 8,594,363-11,682,138 , GRCh38.p12 chr7: 8,554,733-11,642,511 PHF14, THSD7A, 22 more genes
    nsv6631363copy number variation1nstd224human GRCh37 chr7: 10,975,011-10,991,660 , GRCh38.p12 chr7: 10,935,384-10,952,033 LOC107986767, NDUFA4
    nsv6631362copy number variation1nstd224human GRCh37 chr7: 10,910,808-11,036,554 , GRCh38.p12 chr7: 10,871,181-10,996,927 NDUFA4, PHF14, 1 more genes
    nsv6631352copy number variation1nstd224human GRCh37 chr7: 10,042,560-10,979,396 , GRCh38.p12 chr7: 10,002,933-10,939,769 NDUFA4, MGC4859, 7 more genes
    nsv6631301copy number variation1nstd224human GRCh37 chr7: 10,957,622-10,991,660 , GRCh38.p12 chr7: 10,917,995-10,952,033 LOC107986767, NDUFA4
    nsv6615309copy number variation1nstd223human GRCh38 chr7: 10,877,448-10,966,787 , GRCh37.p13 chr7: 10,917,075-11,006,414 LOC107986767, NDUFA4
    nsv6607076copy number variation1nstd223human GRCh38 chr7: 10,873,758-10,995,065 , GRCh37.p13 chr7: 10,913,385-11,034,692 PHF14, NDUFA4, 1 more genes
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