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Items: 1 to 20 of 963

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7098738copy number variation1nstd102humanUncertain significance GRCh37 chr7: 151,832,009-151,962,122 , GRCh38.p12 chr7: 152,134,924-152,265,037 KMT2C
    nsv7097876copy number variation1nstd102humanUncertain significance GRCh37 chr7: 152,132,691-152,373,164 , GRCh38.p12 chr7: 152,435,606-152,676,079 FABP5P3, RPS20P19, 6 more genes
    nsv7097875copy number variation1nstd102humanUncertain significance GRCh37 chr7: 151,680,051-151,856,177 , GRCh38.p12 chr7: 151,982,966-152,159,092 LOC731075, GALNT11, 3 more genes
    nsv7097874copy number variation1nstd102humanUncertain significance GRCh37 chr7: 151,664,332-151,842,400 , GRCh38.p12 chr7: 151,967,247-152,145,315 YBX1P4, GALNT11, 3 more genes
    nsv7097872copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 150,324,807-152,373,164 , GRCh38.p12 chr7: 150,627,719-152,676,079 CRYGN, MIR3907, 57 more genes
    nsv7097728copy number variation1nstd102humanUncertain significance GRCh37 chr7: 151,921,080-152,132,871 , GRCh38.p12 chr7: 152,223,995-152,435,786 FABP5P3, KMT2C, 1 more genes
    nsv7097494copy number variation1nstd102humanUncertain significance GRCh37 chr7: 151,704,892-152,373,164 , GRCh38.p12 chr7: 152,007,807-152,676,079 GALNTL5, GALNT11, 11 more genes
    nsv7097492copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,307,047-152,613,597 , GRCh38.p12 chr7: 150,609,959-152,916,512 PRKAG2, CDK5, 61 more genes
    nsv7097354copy number variation1nstd102humanLikely benign GRCh37 chr7: 151,833,917-152,055,780 , GRCh38.p12 chr7: 152,136,832-152,358,695 KMT2C
    nsv7097353copy number variation1nstd102humanUncertain significance GRCh37 chr7: 151,833,917-151,960,235 , GRCh38.p12 chr7: 152,136,832-152,263,150 KMT2C
    nsv7093188copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 151,871,328-151,935,791 , GRCh38.p12 chr7: 152,174,243-152,238,706 KMT2C
    nsv7077682inversion1nstd229human GRCh38 chr7: 152,020,450-152,223,639 , GRCh37.p13 chr7: 151,717,535-151,920,724 KMT2C, LOC731075, 2 more genes
    nsv7076338inversion1nstd229human GRCh38 chr7: 151,993,087-152,292,059 , GRCh37.p13 chr7: 151,690,172-151,989,144 GALNT11, LOC731075, 3 more genes
    nsv7075139inversion1nstd229human GRCh38 chr7: 152,313,130-152,313,162 , GRCh37.p13 chr7: 152,010,215-152,010,247 KMT2C
    nsv7073389inversion1nstd229human GRCh38 chr7: 152,306,089-152,316,854 , GRCh37.p13 chr7: 152,003,174-152,013,939 KMT2C
    nsv7073211inversion1nstd229human GRCh38 chr7: 151,972,764-152,376,861 , GRCh37.p13 chr7: 151,669,849-152,073,946 GALNTL5, LOC731075, 4 more genes
    nsv7068296inversion1nstd229human GRCh38 chr7: 152,349,214-152,430,816 , GRCh37.p13 chr7: 152,046,299-152,127,901 KMT2C, SEPTIN7P6
    nsv7066025inversion1nstd229human GRCh38 chr7: 152,262,761-152,364,819 , GRCh37.p13 chr7: 151,959,846-152,061,904 KMT2C
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