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Items: 1 to 20 of 402

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148244copy number variation1nstd102humanPathogenic GRCh38 chr15: 82,130,136-82,727,529 , GRCh37.p13 chr15: 82,422,477-83,396,281 CPEB1-AS1, LOC338963, 22 more genes
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7094736copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,545,012-82,554,119 , GRCh38.p12 chr15: 82,252,671-82,261,778 SAXO2, EFL1
    nsv7094637copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,456,174-82,554,119 , GRCh38.p12 chr15: 82,163,833-82,261,778 SAXO2, RNU1-77P, 1 more genes
    nsv7094309copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,511,973-82,512,590 , GRCh38.p12 chr15: 82,219,632-82,220,249 EFL1
    nsv7071284inversion1nstd229human GRCh38 chr15: 82,250,854-84,092,439 , GRCh37.p13 chr15: 82,543,195-84,761,191 HOMER2, EFL1, 46 more genes
    nsv7065621inversion1nstd229human GRCh38 chr15: 82,095,732-82,527,005 , GRCh37.p13 chr15: 82,388,073-82,811,413 RNU1-77P, DNM1P36, 16 more genes
    nsv7065371inversion1nstd229human GRCh38 chr15: 82,262,265-85,274,261 , GRCh37.p13 chr15: 82,554,606-85,817,492 GOLGA6L10, GOLGA6L17P, 96 more genes
    nsv7065029inversion1nstd229human GRCh38 chr15: 82,228,822-82,401,956 , GRCh37.p13 chr15: 82,521,163-82,694,167 EFL1, RPL9P8, 5 more genes
    nsv7063845inversion1nstd229human GRCh38 chr15: 82,252,671-83,794,124 , GRCh37.p13 chr15: 82,545,012-84,462,876 CSPG4P10, DNM1P36, 42 more genes
    nsv7063322inversion1nstd229human GRCh38 chr15: 81,455,725-83,007,733 , GRCh37.p13 chr15: 81,748,066-83,676,485 GOLGA6L10, DNM1P38, 39 more genes
    nsv7063132inversion1nstd229human GRCh38 chr15: 82,261,447-84,086,720 , GRCh37.p13 chr15: 82,553,788-84,755,472 GOLGA6L10, DNM1P38, 46 more genes
    nsv7062899inversion1nstd229human GRCh38 chr15: 82,051,995-82,296,909 , GRCh37.p13 chr15: 82,344,336-82,589,247 SAXO2, ADAMTS7P1, 4 more genes
    nsv7058879inversion1nstd229human GRCh38 chr15: 82,197,935-85,119,504 , GRCh37.p13 chr15: 82,490,276-85,662,735 LOC103171574, RN7SL417P, 87 more genes
    nsv6976365copy number variation1nstd229human GRCh38 chr15: 82,202,360-82,202,713 , GRCh37.p13 chr15: 82,494,701-82,495,054 EFL1
    nsv6964633copy number variation1nstd229human GRCh38 chr15: 82,261,701-82,266,500 , GRCh37.p13 chr15: 82,554,042-82,558,841 SAXO2, EFL1
    nsv6964308copy number variation1nstd229human GRCh38 chr15: 82,206,829-82,206,908 , GRCh37.p13 chr15: 82,499,170-82,499,249 EFL1
    nsv6962285copy number variation1nstd229human GRCh38 chr15: 82,152,633-82,157,928 , GRCh37.p13 chr15: 82,444,974-82,450,269 EFL1
    nsv6958407copy number variation1nstd229human GRCh38 chr15: 82,255,211-82,317,429 , GRCh37.p13 chr15: 82,547,552-82,609,765 SAXO2, EFL1, 1 more genes
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