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Items: 1 to 20 of 1102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137123copy number variation1nstd102humanPathogenic GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046 SLC26A7, LOC105375639, 112 more genes
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7075350inversion1nstd229human GRCh38 chr8: 97,169,552-97,196,815 , GRCh37.p13 chr8: 98,181,780-98,209,043 LOC101927066
    nsv7072732inversion1nstd229human GRCh38 chr8: 97,247,151-97,253,405 , GRCh37.p13 chr8: 98,259,379-98,265,633 LOC101927066
    nsv7072181inversion1nstd229human GRCh38 chr8: 94,465,642-98,351,757 , GRCh37.p13 chr8: 95,477,870-99,363,985 SDC2, LOC100286997, 59 more genes
    nsv7070195inversion1nstd229human GRCh38 chr8: 97,015,930-97,277,239 , GRCh37.p13 chr8: 98,028,158-98,289,467 TSPYL5, LOC101927066, 2 more genes
    nsv7070105inversion1nstd229human GRCh38 chr8: 97,443,932-97,454,983 , GRCh37.p13 chr8: 98,456,160-98,467,211 LOC101927066
    nsv7069177inversion1nstd229human GRCh38 chr8: 97,413,687-97,414,259 , GRCh37.p13 chr8: 98,425,915-98,426,487 LOC101927066
    nsv7068077inversion1nstd229human GRCh38 chr8: 97,167,554-97,184,128 , GRCh37.p13 chr8: 98,179,782-98,196,356 LOC101927066
    nsv7065485inversion1nstd229human GRCh38 chr8: 97,240,924-97,405,096 , GRCh37.p13 chr8: 98,253,152-98,417,324 SNORD3H, TSPYL5, 1 more genes
    nsv7063672inversion1nstd229human GRCh38 chr8: 97,228,209-97,241,041 , GRCh37.p13 chr8: 98,240,437-98,253,269 LOC101927066
    nsv7062158inversion1nstd229human GRCh38 chr8: 97,050,931-97,056,882 , GRCh37.p13 chr8: 98,063,159-98,069,110 LOC101927066, CPQ
    nsv7061371inversion1nstd229human GRCh38 chr8: 97,038,749-97,302,138 , GRCh37.p13 chr8: 98,050,977-98,314,366 CPQ, TSPYL5, 2 more genes
    nsv7060345inversion1nstd229human GRCh38 chr8: 96,974,488-96,978,568 , GRCh37.p13 chr8: 97,986,716-97,990,796 CPQ, LOC101927066
    nsv6858045copy number variation1nstd229human GRCh38 chr8: 97,061,358-97,061,385 , GRCh37.p13 chr8: 98,073,586-98,073,613 CPQ, LOC101927066
    nsv6857360copy number variation1nstd229human GRCh38 chr8: 97,187,929-97,188,236 , GRCh37.p13 chr8: 98,200,157-98,200,464 LOC101927066
    nsv6855654copy number variation1nstd229human GRCh38 chr8: 97,354,667-97,357,047 , GRCh37.p13 chr8: 98,366,895-98,369,275 SNORD3H, LOC101927066
    nsv6855607copy number variation1nstd229human GRCh38 chr8: 96,965,763-96,966,316 , GRCh37.p13 chr8: 97,977,991-97,978,544 CPQ, LOC101927066
    nsv6854704copy number variation1nstd229human GRCh38 chr8: 96,976,258-96,976,348 , GRCh37.p13 chr8: 97,988,486-97,988,576 CPQ, LOC101927066
    nsv6853317copy number variation1nstd229human GRCh38 chr8: 97,372,288-97,465,636 , GRCh37.p13 chr8: 98,384,516-98,477,864 LOC101927066
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