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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7064385inversion1nstd229human GRCh38 chr8: 33,508,845-34,133,580 , GRCh37.p13 chr8: 33,366,363-33,991,098 LOC105379364, LOC100630919, 11 more genes
    nsv6857294copy number variation1nstd229human GRCh38 chr8: 33,516,917-33,553,012 , GRCh37.p13 chr8: 33,374,435-33,410,530 LOC100630919, RPL10P18, 1 more genes
    nsv6856039copy number variation1nstd229human GRCh38 chr8: 33,557,301-33,603,700 , GRCh37.p13 chr8: 33,414,819-33,461,218 RN7SL621P, RNF122, 1 more genes
    nsv6848357copy number variation1nstd229human GRCh38 chr8: 33,539,866-33,583,378 , GRCh37.p13 chr8: 33,397,384-33,440,896 RN7SL621P, RNF122, 1 more genes
    nsv6847226copy number variation1nstd229human GRCh38 chr8: 32,865,701-33,913,200 , GRCh37.p13 chr8: 32,723,219-33,770,718 DUSP26, LOC105379362, 20 more genes
    nsv6845325copy number variation1nstd229human GRCh38 chr8: 33,560,687-33,562,675 , GRCh37.p13 chr8: 33,418,205-33,420,193 RNF122
    nsv6844963copy number variation1nstd229human GRCh38 chr8: 33,560,912-33,570,758 , GRCh37.p13 chr8: 33,418,430-33,428,276 RNF122
    nsv6844498copy number variation1nstd229human GRCh38 chr8: 33,293,571-33,565,874 , GRCh37.p13 chr8: 33,151,089-33,423,392 TTI2, RNF122, 7 more genes
    nsv6838203copy number variation1nstd229human GRCh38 chr8: 33,554,259-33,557,566 , GRCh37.p13 chr8: 33,411,777-33,415,084 RNF122
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6429596copy number variation1nstd223human GRCh38 chr8: 33,560,501-33,562,800 , GRCh37.p13 chr8: 33,418,019-33,420,318 RNF122
    nsv6417531copy number variation1nstd223human GRCh38 chr8: 33,562,001-33,562,600 , GRCh37.p13 chr8: 33,419,519-33,420,118 RNF122
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6302120copy number variation1nstd186human GRCh37 chr8: 33,418,186-33,420,174 , GRCh38.p12 chr8: 33,560,668-33,562,656 RNF122
    nsv6137272copy number variation1nstd213human GRCh37 chr8: 26,370,000-35,590,001 , GRCh38.p12 chr8: 26,512,484-35,732,483 ADRA1A, CHRNA2, 141 more genes
    nsv6136668copy number variation1nstd213human GRCh37 chr8: 33,400,000-33,780,001 , GRCh38.p12 chr8: 33,542,482-33,922,483 DUSP26, RNF122, 6 more genes
    nsv6136665copy number variation1nstd213human GRCh37 chr8: 30,710,000-33,810,001 , GRCh38.p12 chr8: 30,852,484-33,952,483 NRG1, WRN, 37 more genes
    nsv6136029copy number variation1nstd213human GRCh37 chr8: 26,360,000-35,600,001 , GRCh38.p12 chr8: 26,502,484-35,742,483 ADRA1A, CHRNA2, 141 more genes
    nsv5911009copy number variation1nstd209human GRCh38 chr8: 33,560,668-33,562,655 , GRCh37.p13 chr8: 33,418,186-33,420,173 RNF122
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