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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5517330copy number variation1nstd206human GRCh38 chr17: 75,185,992-75,204,187 , GRCh37.p13 chr17: 73,182,087-73,200,282 NUP85
    nsv5356263translocation1nstd200human GRCh38 chr17: 75,225,033-75,225,033 , GRCh38 chr12: 93,542,088-93,542,088 , GRCh37.p13 chr12: 93,935,864-93,935,864 , GRCh37.p13 chr17: 73,221,128-73,221,128 NUP85, GGA3
    nsv5356262translocation1nstd200human GRCh38 chr17: 75,223,675-75,223,675 , GRCh38 chr12: 93,542,087-93,542,087 , GRCh37.p13 chr17: 73,219,770-73,219,770 , GRCh37.p13 chr12: 93,935,863-93,935,863 NUP85, GGA3
    nsv5298973copy number variation1nstd204human GRCh38.p13 chr17: 74,951,501-75,212,200 , GRCh37.p13 chr17: 72,947,596-73,208,295 RNU6-362P, TRR-CCT2-1, 17 more genes
    nsv5296775copy number variation1nstd204human GRCh38.p13 chr17: 75,212,601-75,224,000 , GRCh37.p13 chr17: 73,208,696-73,220,095 GGA3, NUP85
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5285175copy number variation1nstd204human GRCh38.p13 chr17: 75,213,501-75,463,000 , GRCh37.p13 chr17: 73,209,596-73,459,081 MIR3678, MIF4GD-DT, 9 more genes
    nsv5283989copy number variation1nstd204human GRCh38.p13 chr17: 75,210,731-75,213,000 , GRCh37.p13 chr17: 73,206,826-73,209,095 NUP85
    nsv5283056copy number variation1nstd204human GRCh38.p13 chr17: 75,211,431-75,213,650 , GRCh37.p13 chr17: 73,207,526-73,209,745 NUP85
    nsv5197582mobile element insertion1nstd203human GRCh38 chr17: 75,227,955-75,227,955 , GRCh37.p13 chr17: 73,224,050-73,224,050 GGA3, NUP85
    nsv5159166mobile element insertion1nstd203human GRCh38 chr17: 75,205,011-75,205,021 , GRCh37.p13 chr17: 73,201,106-73,201,116 NUP85
    nsv5155047mobile element insertion1nstd203human GRCh38 chr17: 75,235,336-75,235,354 , GRCh37.p13 chr17: 73,231,431-73,231,449 GGA3, NUP85
    nsv5149010mobile element insertion1nstd203human GRCh38 chr17: 75,220,262-75,220,281 , GRCh37.p13 chr17: 73,216,357-73,216,376 NUP85
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5016672copy number variation1nstd200human GRCh38 chr17: 75,222,809-75,224,561 , GRCh37.p13 chr17: 73,218,904-73,220,656 GGA3, NUP85
    nsv5014010copy number variation1nstd200human GRCh38 chr17: 75,062,121-75,491,883 , GRCh37.p13 chr17: 73,058,216-73,487,964 NUP85, RNU6-938P, 17 more genes
    nsv4858966copy number variation1nstd200human GRCh37 chr17: 73,218,902-73,220,658 , GRCh38.p12 chr17: 75,222,807-75,224,563 GGA3, NUP85
    nsv4858965copy number variation1nstd200human GRCh37 chr17: 73,202,933-73,203,343 , GRCh38.p12 chr17: 75,206,838-75,207,248 NUP85
    nsv4854385copy number variation1nstd200human GRCh37 chr17: 73,058,216-73,487,964 , GRCh38.p12 chr17: 75,062,121-75,491,883 LOC107985034, SUMO2, 17 more genes
    nsv4676207copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,218,219-73,443,987 , GRCh38.p12 chr17: 75,222,124-75,447,906 GGA3, TMEM94, 9 more genes
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