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Items: 1 to 20 of 234

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    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
    nsv7077902inversion1nstd229human GRCh38 chr8: 24,399,029-24,691,520 , GRCh37.p13 chr8: 24,256,542-24,549,033 ADAMDEC1, ADAM7-AS2, 4 more genes
    nsv7069164inversion1nstd229human GRCh38 chr8: 24,398,247-24,398,314 , GRCh37.p13 chr8: 24,255,760-24,255,827 ADAM7-AS1, ADAMDEC1
    nsv6854382copy number variation1nstd229human GRCh38 chr8: 24,360,937-25,091,878 , GRCh37.p13 chr8: 24,218,450-24,949,393 ADAM7-AS2, ADAMDEC1, 10 more genes
    nsv6850922copy number variation1nstd229human GRCh38 chr8: 24,398,889-24,401,313 , GRCh37.p13 chr8: 24,256,402-24,258,826 ADAM7-AS1, ADAMDEC1
    nsv6850838copy number variation1nstd229human GRCh38 chr8: 24,393,909-24,424,831 , GRCh37.p13 chr8: 24,251,422-24,282,344 ADAMDEC1, ADAM7-AS1
    nsv6848074copy number variation1nstd229human GRCh38 chr8: 24,222,214-24,544,146 , GRCh37.p13 chr8: 24,079,727-24,401,659 ADAM28, ADAM7, 4 more genes
    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
    nsv6432093copy number variation1nstd223human GRCh38 chr8: 24,288,590-24,635,500 , GRCh37.p13 chr8: 24,146,103-24,493,013 ADAM7-AS1, ADAM28, 4 more genes
    nsv6427546copy number variation1nstd223human GRCh38 chr8: 24,390,901-24,391,900 , GRCh37.p13 chr8: 24,248,414-24,249,413 ADAM7-AS1, ADAMDEC1
    nsv6425290copy number variation1nstd223human GRCh38 chr8: 24,402,801-24,403,800 , GRCh37.p13 chr8: 24,260,314-24,261,313 ADAMDEC1, ADAM7-AS1
    nsv6424587copy number variation1nstd223human GRCh38 chr8: 24,382,801-24,383,800 , GRCh37.p13 chr8: 24,240,314-24,241,313 ADAMDEC1, ADAM7-AS1
    nsv6422718copy number variation1nstd223human GRCh38 chr8: 24,385,025-24,385,543 , GRCh37.p13 chr8: 24,242,538-24,243,056 ADAM7-AS1, ADAMDEC1
    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
    nsv6290971copy number variation1nstd102humanUncertain significance GRCh37 chr8: 24,221,648-24,947,015 , GRCh38.p12 chr8: 24,364,135-25,089,500 LOC105379329, LOC105379330, 10 more genes
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