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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148088copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,263,507-27,829,791 , GRCh38.p12 chr17: 26,936,481-29,502,773 RNU4-34P, RNU6-711P, 95 more genes
    nsv7145449copy number variation1nstd232human GRCh37.p13 chr17: 27,209,046-27,209,134 , GRCh38.p12 chr17: 28,882,028-28,882,116 FLOT2
    nsv7139265insertion1nstd232human GRCh37.p13 chr17: 27,207,884-27,207,884 , GRCh38.p12 chr17: 28,880,866-28,880,866 FLOT2
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7094962copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-27,581,367 , GRCh38.p12 chr17: 28,357,671-29,254,349 FLOT2, SPAG5-AS1, 50 more genes
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6991473copy number variation1nstd229human GRCh38 chr17: 28,876,147-28,896,575 , GRCh37.p13 chr17: 27,203,165-27,223,593 DHRS13, FLOT2
    nsv6988295copy number variation1nstd229human GRCh38 chr17: 28,875,176-28,877,607 , GRCh37.p13 chr17: 27,202,194-27,204,625 FLOT2
    nsv6988000copy number variation1nstd229human GRCh38 chr17: 28,889,619-28,890,947 , GRCh37.p13 chr17: 27,216,637-27,217,965 FLOT2
    nsv6982094copy number variation1nstd229human GRCh38 chr17: 28,894,606-28,898,183 , GRCh37.p13 chr17: 27,221,624-27,225,201 FLOT2, DHRS13
    nsv6981917copy number variation1nstd229human GRCh38 chr17: 28,805,032-28,929,082 , GRCh37.p13 chr17: 27,132,050-27,256,100 MIR451A, FAM222B, 8 more genes
    nsv6979186copy number variation1nstd229human GRCh38 chr17: 28,889,188-28,901,491 , GRCh37.p13 chr17: 27,216,206-27,228,509 DHRS13, FLOT2
    nsv6502735copy number variation1nstd223human GRCh38 chr17: 28,889,672-28,890,894 , GRCh37.p13 chr17: 27,216,690-27,217,912 FLOT2
    nsv6498281copy number variation1nstd223human GRCh38 chr17: 28,888,293-28,925,540 , GRCh37.p13 chr17: 27,215,311-27,252,558 LOC101927018, FLOT2, 2 more genes
    nsv6314042copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-28,281,232 , GRCh38.p12 chr17: 22,164,047-29,954,214 TAOK1, TNFAIP1, 131 more genes
    nsv6250722mobile element insertion1nstd215human GRCh38 chr17: 28,878,626-28,878,626 , GRCh37.p13 chr17: 27,205,644-27,205,644 FLOT2
    nsv6133232copy number variation1nstd213human GRCh37 chr17: 26,970,000-27,750,001 , GRCh38.p12 chr17: 28,642,982-29,422,983 CRYBA1, FLOT2, 37 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv6133228copy number variation1nstd213human GRCh37 chr17: 25,300,000-27,290,001 , GRCh38.p12 chr17: 26,972,974-28,962,983 LGALS9, RPL23A, 82 more genes
    nsv5946772copy number variation1nstd209human GRCh38 chr17: 28,875,152-28,877,606 , GRCh37.p13 chr17: 27,202,170-27,204,624 FLOT2
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