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Items: 1 to 20 of 1075

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7148110copy number variation1nstd102humanPathogenic GRCh37 chr8: 7,080,281-12,045,269 , GRCh38.p12 chr8: 7,222,759-12,187,760 DEFB106A, LOC101927997, 176 more genes
    nsv7074774inversion1nstd229human GRCh38 chr8: 7,765,163-10,984,073 , GRCh37.p13 chr8: 7,622,685-10,841,583 PRSS52P, PPP1R3B-DT, 81 more genes
    nsv7071894inversion1nstd229human GRCh38 chr8: 8,228,418-10,333,532 , GRCh37.p13 chr8: 8,085,940-10,191,042 RN7SL178P, LOC107986914, 33 more genes
    nsv7069609inversion1nstd229human GRCh38 chr8: 7,102,414-12,683,056 , GRCh37.p13 chr8: 6,959,936-12,540,565 FAM90A20, LOC107986910, 201 more genes
    nsv7067997inversion1nstd229human GRCh38 chr8: 8,181,479-12,388,066 , GRCh37.p13 chr8: 8,039,001-12,245,575 TNKS, ZNF705D, 113 more genes
    nsv7062815inversion1nstd229human GRCh38 chr8: 8,907,885-8,907,916 , GRCh37.p13 chr8: 8,765,395-8,765,426 ERI1
    nsv7062538inversion1nstd229human GRCh38 chr8: 7,137,678-12,551,118 , GRCh37.p13 chr8: 6,995,200-12,408,627 MIR124-1, MFHAS1, 197 more genes
    nsv7060774inversion1nstd229human GRCh38 chr8: 7,366,932-11,853,836 , GRCh37.p13 chr8: 7,224,454-11,711,345 DEFB104B, SNORA99, 135 more genes
    nsv7059776inversion1nstd229human GRCh38 chr8: 9,080,355-9,259,206 , GRCh37.p13 chr8: 8,937,865-9,116,716 PPP1R3B-DT, LOC101929128, 3 more genes
    nsv7059146inversion1nstd229human GRCh38 chr8: 7,352,588-12,547,775 , GRCh37.p13 chr8: 7,210,110-12,405,284 LOC107986910, HSPD1P2, 179 more genes
    nsv7058956inversion1nstd229human GRCh38 chr8: 8,224,000-12,734,745 , GRCh37.p13 chr8: 8,081,522-12,592,254 MIR3926-1, FAM90A25P, 129 more genes
    nsv6857771copy number variation1nstd229human GRCh38 chr8: 8,908,517-8,913,950 , GRCh37.p13 chr8: 8,766,027-8,771,460 ERI1
    nsv6856279copy number variation1nstd229human GRCh38 chr8: 8,957,300-9,064,848 , GRCh37.p13 chr8: 8,814,810-8,922,358 ERI1, LOC105379227, 3 more genes
    nsv6855657copy number variation1nstd229human GRCh38 chr8: 8,910,490-8,919,976 , GRCh37.p13 chr8: 8,768,000-8,777,486 ERI1
    nsv6855580copy number variation1nstd229human GRCh38 chr8: 8,997,397-9,002,157 , GRCh37.p13 chr8: 8,854,907-8,859,667 LOC105379227, ERI1
    nsv6855546copy number variation1nstd229human GRCh38 chr8: 8,941,854-8,943,014 , GRCh37.p13 chr8: 8,799,364-8,800,524 ERI1
    nsv6855482copy number variation1nstd229human GRCh38 chr8: 8,897,874-8,904,206 , GRCh37.p13 chr8: 8,755,384-8,761,716 ERI1
    nsv6854725copy number variation1nstd229human GRCh38 chr8: 9,078,680-9,090,987 , GRCh37.p13 chr8: 8,936,190-8,948,497 ERI1
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