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Items: 1 to 20 of 416

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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
    nsv7141428insertion1nstd232human GRCh37.p13 chr8: 25,320,064-25,320,064 , GRCh38.p12 chr8: 25,462,548-25,462,548 CDCA2
    nsv7139880copy number variation1nstd232human GRCh37.p13 chr8: 25,327,221-25,327,277 , GRCh38.p12 chr8: 25,469,705-25,469,761 CDCA2
    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
    nsv7097659copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 24,810,323-25,892,142 , GRCh38.p12 chr8: 24,952,810-26,034,626 LOC105379333, LOC102723395, 13 more genes
    nsv7075516inversion1nstd229human GRCh38 chr8: 24,977,089-26,865,369 , GRCh37.p13 chr8: 24,834,603-26,722,886 ADRA1A, LOC107986933, 25 more genes
    nsv6857590copy number variation1nstd229human GRCh38 chr8: 25,467,387-25,476,292 , GRCh37.p13 chr8: 25,324,903-25,333,808 CDCA2
    nsv6856212copy number variation1nstd229human GRCh38 chr8: 25,492,051-25,492,206 , GRCh37.p13 chr8: 25,349,567-25,349,722 CDCA2
    nsv6855273copy number variation1nstd229human GRCh38 chr8: 25,475,339-25,482,926 , GRCh37.p13 chr8: 25,332,855-25,340,442 CDCA2
    nsv6854371copy number variation1nstd229human GRCh38 chr8: 24,983,501-25,722,900 , GRCh37.p13 chr8: 24,841,015-25,580,416 LOC105379330, CDCA2, 9 more genes
    nsv6853086copy number variation1nstd229human GRCh38 chr8: 25,494,836-25,499,656 , GRCh37.p13 chr8: 25,352,352-25,357,172 CDCA2
    nsv6849524copy number variation1nstd229human GRCh38 chr8: 25,504,745-25,507,857 , GRCh37.p13 chr8: 25,362,261-25,365,373 CDCA2
    nsv6848171copy number variation1nstd229human GRCh38 chr8: 25,490,998-25,496,032 , GRCh37.p13 chr8: 25,348,514-25,353,548 CDCA2
    nsv6844916copy number variation1nstd229human GRCh38 chr8: 25,469,705-25,469,762 , GRCh37.p13 chr8: 25,327,221-25,327,278 CDCA2
    nsv6842619copy number variation1nstd229human GRCh38 chr8: 25,489,774-25,495,787 , GRCh37.p13 chr8: 25,347,290-25,353,303 CDCA2
    nsv6841819copy number variation1nstd229human GRCh38 chr8: 25,493,601-25,499,700 , GRCh37.p13 chr8: 25,351,117-25,357,216 CDCA2
    nsv6839671copy number variation1nstd229human GRCh38 chr8: 25,491,762-25,498,354 , GRCh37.p13 chr8: 25,349,278-25,355,870 CDCA2
    nsv6838486copy number variation1nstd229human GRCh38 chr8: 25,424,840-25,525,676 , GRCh37.p13 chr8: 25,282,356-25,383,192 GNRH1, KCTD9, 1 more genes
    nsv6636762copy number variation1nstd102humanUncertain significance GRCh37 chr8: 25,232,694-25,511,821 , GRCh38.p12 chr8: 25,375,178-25,654,305 CDCA2, LOC107986933, 3 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
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