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Items: 1 to 20 of 153

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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
    nsv6854469copy number variation1nstd229human GRCh38 chr8: 33,496,222-33,541,787 , GRCh37.p13 chr8: 33,353,740-33,399,305 TTI2, RPL10P18, 3 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
    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
    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
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    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
    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
    nsv6136037copy number variation1nstd213human GRCh37 chr8: 33,300,000-33,400,001 , GRCh38.p12 chr8: 33,442,482-33,542,483 TTI2, MAK16, 4 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
    nsv6017004copy number variation1nstd212human GRCh38 chr8: 33,513,955-33,515,013 , GRCh37.p13 chr8: 33,371,473-33,372,531 SNORD13
    nsv5925166copy number variation1nstd209human GRCh38 chr8: 33,513,955-33,515,012 , GRCh37.p13 chr8: 33,371,473-33,372,530 SNORD13
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4960076copy number variation1nstd200human GRCh38 chr8: 33,513,958-33,515,013 , GRCh37.p13 chr8: 33,371,476-33,372,531 SNORD13
    nsv4960074copy number variation1nstd200human GRCh38 chr8: 33,506,533-33,529,639 , GRCh37.p13 chr8: 33,364,051-33,387,157 SNORD13, LOC100630919, 1 more genes
    nsv4954317copy number variation1nstd200human GRCh38 chr8: 33,293,571-33,565,876 , GRCh37.p13 chr8: 33,151,089-33,423,394 TTI2, FUT10, 7 more genes
    nsv4827316copy number variation1nstd200human GRCh37 chr8: 33,371,476-33,372,531 , GRCh38.p12 chr8: 33,513,958-33,515,013 SNORD13
    nsv4769375copy number variation1nstd102humanUncertain significance GRCh37 chr8: 32,691,933-33,893,567 , GRCh38.p12 chr8: 32,834,415-34,036,049 SNORD13, BUD31P1, 21 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
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