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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4351367copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr17: 24,298,969-27,841,151 , GRCh37.p13 chr17: 27,274,843-30,817,038 , GRCh38.p12 chr17: 28,947,825-32,490,020 SSH2, ALOX12P1, 110 more genes
    nsv4344921sequence alteration1nstd166human GRCh37.p13 chr17: 15,509,955-30,464,674 , GRCh38.p12 chr17: 15,606,641-32,137,655 SSH2, AK4P1, 450 more genes
    nsv4339273mobile element insertion1nstd166human GRCh37.p13 chr17: 28,120,170-28,120,187 , GRCh38.p12 chr17: 29,793,152-29,793,169 SSH2
    nsv4339033sequence alteration1nstd166human GRCh37.p13 chr17: 28,121,618-28,136,025 , GRCh38.p12 chr17: 29,794,600-29,809,007 SSH2
    nsv4338830sequence alteration1nstd166human GRCh37.p13 chr17: 15,070,479-30,207,111 , GRCh38.p12 chr17: 15,167,162-31,880,092 SSH2, ALDOC, 454 more genes
    nsv4338488mobile element insertion1nstd166human GRCh37.p13 chr17: 1,835,270-58,629,509 , GRCh38.p12 chr17: 1,931,976-60,552,148 SSH2, AK4P1, 1797 more genes
    nsv4337573mobile element insertion1nstd166human GRCh37.p13 chr17: 27,671,522-75,772,056 , GRCh38.p12 chr17: 29,344,504-77,775,974 SSH2, CACNB1, 1429 more genes
    nsv4336077sequence alteration1nstd166human GRCh37.p13 chr17: 15,509,892-30,464,766 , GRCh38.p12 chr17: 15,606,578-32,137,747 SSH2, ALDH3A1, 450 more genes
    nsv4333470mobile element insertion1nstd166human GRCh37.p13 chr17: 27,960,735-27,960,749 , GRCh38.p12 chr17: 29,633,717-29,633,731 SSH2
    nsv4331669insertion1nstd166human GRCh37.p13 chr17: 16,248,738-71,328,511 , GRCh38.p12 chr17: 16,345,424-73,332,372 SSH2, AP2B1, 1603 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 SSH2, AP2B1, 1499 more genes
    nsv4329581insertion1nstd166human GRCh37.p13 chr17: 5,419,390-49,304,628 , GRCh38.p12 chr17: 5,516,070-51,227,267 SSH2, ACACA, 1490 more genes
    nsv4329451insertion1nstd166human GRCh37.p13 chr17: 6,271,416-79,578,012 , GRCh38.p12 chr17: 6,368,096-81,610,986 SSH2, ACADVL, 2160 more genes
    nsv4328337insertion1nstd166human GRCh37.p13 chr17: 9,384,214-48,751,273 , GRCh38.p12 chr17: 9,480,897-50,673,912 SSH2, AK4P1, 1296 more genes
    nsv4322504insertion1nstd166human GRCh37.p13 chr17: 28,193,213-28,193,233 , GRCh38.p12 chr17: 29,866,195-29,866,215 SSH2
    nsv4322279insertion1nstd166human GRCh37.p13 chr17: 4,813,448-73,107,697 , GRCh38.p12 chr17: 4,910,153-75,111,602 SSH2, AK4P1, 1986 more genes
    nsv4316001mobile element insertion1nstd166human GRCh37.p13 chr17: 28,209,007-28,209,019 , GRCh38.p12 chr17: 29,881,989-29,882,001 SSH2
    nsv4313557mobile element insertion1nstd166human GRCh37.p13 chr17: 28,170,088-28,170,104 , GRCh38.p12 chr17: 29,843,070-29,843,086 SSH2
    nsv4252368copy number variation1nstd166human GRCh37.p13 chr17: 27,962,214-27,962,650 , GRCh38.p12 chr17: 29,635,196-29,635,632 SSH2
    nsv4249502copy number variation1nstd166human GRCh37.p13 chr17: 28,093,883-28,093,945 , GRCh38.p12 chr17: 29,766,865-29,766,927 SSH2
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