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  • The following term was not found in dbVar: Diethanolamine.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309699copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr14: 67,243,162-67,490,412 , GRCh38.p12 chr14: 66,776,444-67,023,695 GPHN
    nsv7094342copy number variation1nstd102humanPathogenic GRCh37 chr14: 67,291,172-67,490,412 , GRCh38.p12 chr14: 66,824,454-67,023,695 GPHN
    nsv3880948copy number variation1nstd102humanPathogenic GRCh37 chr14: 67,243,182-67,432,042 , GRCh38.p12 chr14: 66,776,464-66,965,325 GPHN
    nsv4683736copy number variation1nstd102humanPathogenic GRCh37 chr14: 66,975,226-67,147,923 , GRCh38.p12 chr14: 66,508,508-66,681,205 GPHN
    nsv3881408copy number variation1nstd102humanPathogenic GRCh37 chr14: 67,243,162-67,391,029 , GRCh38.p12 chr14: 66,776,444-66,924,312 GPHN
    nsv6309356copy number variation1nstd102humanPathogenic GRCh37 chr14: 67,346,637-67,432,062 , GRCh38.p12 chr14: 66,879,919-66,965,345 GPHN
    nsv6309765copy number variation1nstd102humanPathogenic GRCh37 chr14: 67,490,330-67,555,812 , GRCh38.p12 chr14: 67,023,613-67,089,095 GPHN
    nsv6309764copy number variation1nstd102humanPathogenic GRCh37 chr14: 67,382,700-67,432,062 , GRCh38.p12 chr14: 66,915,983-66,965,345 GPHN
    nsv5672815copy number variation1nstd102humanPathogenic GRCh37 chr14: 67,243,172-67,291,294 , GRCh38.p12 chr14: 66,776,454-66,824,576 GPHN
    nsv7094146copy number variation1nstd102humanPathogenic GRCh37 chr12: 56,396,006-56,396,524 , GRCh38.p12 chr12: 56,002,222-56,002,740 SUOX
    nsv4453045copy number variation1nstd102humanPathogenic GRCh37 chr14: 67,346,637-67,346,771 , GRCh38 chr14: 66,879,919-66,880,053 GPHN
    nsv4681983copy number variation1nstd102humanPathogenic GRCh37 chr14: 66,975,226-66,975,329 , GRCh38.p12 chr14: 66,508,508-66,508,611 GPHN
    nsv4683676copy number variation1nstd102humanPathogenic GRCh37 chr14: 67,243,162-67,243,259 , GRCh38.p12 chr14: 66,776,444-66,776,541 GPHN
    nsv7093281copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 39,877,645-39,878,462 , GRCh38 chr6: 39,909,901-39,910,718 MOCS1
    nsv7093321copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 67,389,513-67,389,803 , GRCh38 chr14: 66,922,796-66,923,086 GPHN
    nsv3883177copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 67,291,192-67,291,284 , GRCh38 chr14: 66,824,474-66,824,566 GPHN
    nsv3871674copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 67,243,182-67,243,239 , GRCh38 chr14: 66,776,464-66,776,521 GPHN
    nsv6309555copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 67,431,888-67,525,523 , GRCh38.p12 chr14: 66,965,171-67,058,806 GPHN
    nsv6312578copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 39,895,048-39,895,317 , GRCh38.p12 chr6: 39,927,309-39,927,578 MOCS1
    nsv4682299copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 67,382,700-67,382,806 , GRCh38.p12 chr14: 66,915,983-66,916,089 GPHN
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    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
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