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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137156copy number variation1nstd233human GRCh37.p13 chr17: 59,529,098-60,599,347 , GRCh38 chr17: 61,451,737-62,521,986 TBX4, MED13, 20 more genes
    nsv7070986inversion1nstd229human GRCh38 chr17: 59,331,393-62,738,993 , GRCh37.p13 chr17: 57,408,754-60,816,354 MIR21, LINC01476, 83 more genes
    nsv7070223inversion1nstd229human GRCh38 chr17: 61,482,736-62,369,304 , GRCh37.p13 chr17: 59,560,097-60,446,665 TBC1D3P2, TBX4, 12 more genes
    nsv6996688copy number variation1nstd229human GRCh38 chr17: 62,371,209-62,378,799 , GRCh37.p13 chr17: 60,448,570-60,456,160 LOC105371854, EFCAB3
    nsv6991004copy number variation1nstd229human GRCh38 chr17: 62,404,907-62,411,167 , GRCh37.p13 chr17: 60,482,268-60,488,528 EFCAB3
    nsv6982985copy number variation1nstd229human GRCh38 chr17: 62,391,057-62,395,444 , GRCh37.p13 chr17: 60,468,418-60,472,805 RPS23P7, EFCAB3
    nsv6637728copy number variation1nstd102humanUncertain significance GRCh37 chr17: 60,070,415-60,450,079 , GRCh38.p12 chr17: 61,993,054-62,372,718 MED13, LOC100996361, 8 more genes
    nsv6582203inversion1nstd223human GRCh38 chr17: 62,409,357-62,409,704 , GRCh37.p13 chr17: 60,486,718-60,487,065 EFCAB3
    nsv6531727copy number variation1nstd223human GRCh38 chr17: 62,406,471-62,417,664 , GRCh37.p13 chr17: 60,483,832-60,495,025 EFCAB3
    nsv6531321copy number variation1nstd223human GRCh38 chr17: 61,981,221-62,425,637 , GRCh37.p13 chr17: 60,058,582-60,502,998 TBC1D3P2, RPL36AP47, 13 more genes
    nsv6524685copy number variation1nstd223human GRCh38 chr17: 62,404,151-62,412,276 , GRCh37.p13 chr17: 60,481,512-60,489,637 EFCAB3
    nsv6288022insertion1nstd214human GRCh38 chr17: 62,398,096-62,398,096 , GRCh37.p13 chr17: 60,475,457-60,475,457 RPS23P7, EFCAB3
    nsv6144789copy number variation1nstd206human GRCh38 chr17: 62,398,096-62,398,158 , GRCh37.p13 chr17: 60,475,457-60,475,519 RPS23P7, EFCAB3
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv6116175mobile element insertion1nstd186human GRCh37 chr17: 60,483,427-60,483,478 , GRCh38.p12 chr17: 62,406,066-62,406,117 EFCAB3
    nsv5944871copy number variation1nstd209human GRCh38 chr17: 62,398,096-62,398,157 , GRCh37.p13 chr17: 60,475,457-60,475,518 RPS23P7, EFCAB3
    nsv5944166copy number variation1nstd209human GRCh38 chr17: 62,396,361-62,397,824 , GRCh37.p13 chr17: 60,473,722-60,475,185 RPS23P7, EFCAB3
    nsv5938345copy number variation1nstd209human GRCh38 chr17: 62,409,942-62,410,263 , GRCh37.p13 chr17: 60,487,303-60,487,624 EFCAB3
    nsv5931979copy number variation1nstd209human GRCh38 chr17: 62,408,651-62,410,152 , GRCh37.p13 chr17: 60,486,012-60,487,513 EFCAB3
    nsv5877494copy number variation1nstd209human GRCh38 chr17: 62,389,181-62,390,538 , GRCh37.p13 chr17: 60,466,542-60,467,899 EFCAB3
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