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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7098176copy number variation1nstd102humanUncertain significance GRCh37 chr8: 43,052,071-43,054,712 , GRCh38.p12 chr8: 43,196,928-43,199,569 HGSNAT
    nsv7097905copy number variation1nstd102humanPathogenic GRCh37 chr8: 43,002,071-43,033,397 , GRCh38.p12 chr8: 43,146,928-43,178,254 RNY5P6, HGSNAT
    nsv7097799copy number variation1nstd102humanUncertain significance GRCh37 chr8: 43,046,597-43,054,712 , GRCh38.p12 chr8: 43,191,454-43,199,569 HGSNAT
    nsv7097798copy number variation1nstd102humanUncertain significance GRCh37 chr8: 43,024,296-43,054,712 , GRCh38.p12 chr8: 43,169,153-43,199,569 HGSNAT
    nsv7097797copy number variation1nstd102humanUncertain significance GRCh37 chr8: 43,002,091-43,159,912 , GRCh38.p12 chr8: 43,146,948-43,304,769 RNY5P6, VN1R45P, 6 more genes
    nsv7097796copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,977,230-43,054,712 , GRCh38.p12 chr8: 43,122,087-43,199,569 POMK, HGSNAT, 1 more genes
    nsv7097795copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,958,692-43,016,670 , GRCh38.p12 chr8: 43,103,549-43,161,527 RNY5P6, HGSNAT, 1 more genes
    nsv7097662copy number variation2nstd102humanUncertain significance GRCh37 chr8: 41,518,984-43,054,712 , GRCh38.p12 chr8: 41,661,466-43,199,569 LOC101059972, IKBKB-DT, 31 more genes
    nsv7097397copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 43,024,386-43,028,855 , GRCh38.p12 chr8: 43,169,243-43,173,712 HGSNAT
    nsv6853289copy number variation1nstd229human GRCh38 chr8: 43,146,822-43,197,137 , GRCh37.p13 chr8: 43,001,965-43,052,280 RNY5P6, HGSNAT
    nsv6846497copy number variation1nstd229human GRCh38 chr8: 43,131,187-43,139,183 , GRCh37.p13 chr8: 42,986,330-42,994,326 HGSNAT
    nsv6637131copy number variation1nstd102humanPathogenic GRCh37 chr8: 42,303,398-43,002,481 , GRCh38.p12 chr8: 42,445,880-43,147,338 RNU1-124P, LOC105379396, 13 more genes
    nsv6633054copy number variation1nstd224human GRCh37 chr8: 42,958,833-43,791,691 , GRCh38.p12 chr8: 43,103,690-43,936,548 POMK, POTEA, 11 more genes
    nsv6633053copy number variation3nstd224human GRCh37 chr8: 42,937,273-43,791,691 , GRCh38.p12 chr8: 43,082,130-43,936,548 POMK, SNX18P27, 12 more genes
    nsv6632990copy number variation2nstd224human GRCh37 chr8: 42,939,989-43,791,691 , GRCh38.p12 chr8: 43,084,846-43,936,548 FNTA, POTEA, 12 more genes
    nsv6632631copy number variation1nstd224human GRCh37 chr8: 43,008,638-43,791,691 , GRCh38.p12 chr8: 43,153,495-43,936,548 VN1R46P, RNY5P6, 10 more genes
    nsv6632563copy number variation4nstd224human GRCh37 chr8: 43,052,839-43,791,691 , GRCh38.p12 chr8: 43,197,696-43,936,548 VN1R46P, LOC100420534, 9 more genes
    nsv6568370inversion1nstd223human GRCh38 chr8: 43,157,659-43,158,238 , GRCh37.p13 chr8: 43,012,802-43,013,381 HGSNAT
    nsv6565539inversion1nstd223human GRCh38 chr8: 43,149,514-43,150,166 , GRCh37.p13 chr8: 43,004,657-43,005,309 HGSNAT
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