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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6896009copy number variation1nstd229human GRCh38 chr10: 97,916,587-97,936,367 , GRCh37.p13 chr10: 99,676,344-99,696,124 CRTAC1
    nsv6897751copy number variation1nstd229human GRCh38 chr10: 98,016,934-98,021,554 , GRCh37.p13 chr10: 99,776,691-99,781,311 CRTAC1
    nsv6671870copy number variation1nstd229human GRCh38 chr2: 65,075,201-65,079,600 , GRCh37.p13 chr2: 65,302,335-65,306,734 CEP68
    nsv6889750copy number variation1nstd229human GRCh38 chr10: 97,987,020-97,991,370 , GRCh37.p13 chr10: 99,746,777-99,751,127 CRTAC1
    nsv6897724copy number variation1nstd229human GRCh38 chr10: 97,919,554-97,923,213 , GRCh37.p13 chr10: 99,679,311-99,682,970 CRTAC1
    nsv6887874copy number variation1nstd229human GRCh38 chr10: 97,930,401-97,933,600 , GRCh37.p13 chr10: 99,690,158-99,693,357 CRTAC1
    nsv6883568copy number variation1nstd229human GRCh38 chr10: 97,997,431-98,000,504 , GRCh37.p13 chr10: 99,757,188-99,760,261 CRTAC1
    nsv6890025copy number variation1nstd229human GRCh38 chr10: 97,916,636-97,919,708 , GRCh37.p13 chr10: 99,676,393-99,679,465 CRTAC1
    nsv6885547copy number variation1nstd229human GRCh38 chr10: 97,958,537-97,961,537 , GRCh37.p13 chr10: 99,718,294-99,721,294 CRTAC1
    nsv6885141copy number variation1nstd229human GRCh38 chr10: 97,985,953-97,988,533 , GRCh37.p13 chr10: 99,745,710-99,748,290 CRTAC1
    nsv6890510copy number variation1nstd229human GRCh38 chr10: 97,946,653-97,948,383 , GRCh37.p13 chr10: 99,706,410-99,708,140 CRTAC1
    nsv6678008copy number variation1nstd229human GRCh38 chr2: 65,058,501-65,060,000 , GRCh37.p13 chr2: 65,285,635-65,287,134 CEP68
    nsv6897038copy number variation1nstd229human GRCh38 chr10: 98,029,502-98,029,530 , GRCh37.p13 chr10: 99,789,259-99,789,287 CRTAC1
    nsv6450244copy number variation1nstd223human GRCh38 chr10: 98,016,934-98,021,550 , GRCh37.p13 chr10: 99,776,691-99,781,307 CRTAC1
    nsv6337159copy number variation1nstd223human GRCh38 chr2: 65,058,494-65,060,006 , GRCh37.p13 chr2: 65,285,628-65,287,140 CEP68
    nsv6354116copy number variation1nstd223human GRCh38 chr2: 65,079,806-65,080,946 , GRCh37.p13 chr2: 65,306,940-65,308,080 CEP68
    nsv6450525copy number variation1nstd223human GRCh38 chr10: 97,957,261-97,957,778 , GRCh37.p13 chr10: 99,717,018-99,717,535 CRTAC1
    nsv6451832copy number variation1nstd223human GRCh38 chr10: 97,983,249-97,983,586 , GRCh37.p13 chr10: 99,743,006-99,743,343 CRTAC1
    nsv6447209copy number variation1nstd223human GRCh38 chr10: 97,963,062-97,963,313 , GRCh37.p13 chr10: 99,722,819-99,723,070 CRTAC1
    nsv6439350copy number variation1nstd223human GRCh38 chr10: 97,956,518-97,956,686 , GRCh37.p13 chr10: 99,716,275-99,716,443 CRTAC1
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    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
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