U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 209

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7098901copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 21,925,038-26,372,195 , GRCh38.p12 chr8: 22,067,527-26,514,679 BMP1, POLR3D, 95 more genes
    nsv7073429inversion1nstd229human GRCh38 chr8: 22,689,880-24,095,801 , GRCh37.p13 chr8: 22,547,393-23,953,314 TNFRSF10B, RNU1-148P, 34 more genes
    nsv6847578copy number variation1nstd229human GRCh38 chr8: 24,069,291-24,086,702 , GRCh37.p13 chr8: 23,926,804-23,944,215 LOC107986931, RNU1-148P
    nsv6847032copy number variation1nstd229human GRCh38 chr8: 24,073,977-24,087,363 , GRCh37.p13 chr8: 23,931,490-23,944,876 LOC107986931, RNU1-148P
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6575183inversion1nstd223human GRCh38 chr8: 23,965,527-24,582,482 , GRCh37.p13 chr8: 23,823,040-24,439,995 ADAM7, ADAM28, 7 more genes
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
    nsv6429716copy number variation1nstd223human GRCh38 chr8: 22,969,514-24,288,515 , GRCh37.p13 chr8: 22,827,027-24,146,028 NKX3-1, LOC107984124, 27 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6315176copy number variation1nstd102humanPathogenic GRCh37 chr8: 19,779,604-26,531,980 , GRCh38.p12 chr8: 19,922,093-26,674,463 TNFRSF10C, TNFRSF10A, 121 more genes
    nsv6137266copy number variation1nstd213human GRCh37 chr8: 22,950,000-24,240,001 , GRCh38.p12 chr8: 23,092,487-24,382,488 TNFRSF10D, CHMP7, 25 more genes
    nsv6137044copy number variation1nstd213human GRCh37 chr8: 12,460,000-33,310,001 , GRCh38.p12 chr8: 12,602,491-33,452,483 NAT1, ASAH1, 322 more genes
    nsv6136655copy number variation1nstd213human GRCh37 chr8: 19,630,000-29,910,001 , GRCh38.p12 chr8: 19,772,489-30,052,485 BMP1, BNIP3L, 194 more genes
    nsv6136570copy number variation1nstd213human GRCh37 chr8: 22,760,000-24,790,001 , GRCh38.p12 chr8: 22,902,487-24,932,488 LOXL2, NEFM, 38 more genes
    nsv6136312copy number variation1nstd213human GRCh37 chr8: 12,460,000-25,900,001 , GRCh38.p12 chr8: 12,602,491-26,042,485 NAT1, NAT2, 195 more genes
    nsv6136241copy number variation1nstd213human GRCh37 chr8: 12,490,000-25,900,001 , GRCh38.p12 chr8: 12,632,491-26,042,485 NAT1, NAT2, 194 more genes
    nsv6009708copy number variation1nstd212human GRCh38 chr8: 24,076,588-24,076,675 , GRCh37.p13 chr8: 23,934,101-23,934,188 LOC107986931, RNU1-148P
    nsv5923483copy number variation1nstd209human GRCh38 chr8: 24,076,518-24,076,669 , GRCh37.p13 chr8: 23,934,031-23,934,182 LOC107986931, RNU1-148P
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center