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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076199inversion1nstd229human GRCh38 chr16: 52,568,731-52,571,026 , GRCh37.p13 chr16: 52,602,643-52,604,938 CASC16
    nsv7073921inversion1nstd229human GRCh38 chr16: 52,564,001-52,575,386 , GRCh37.p13 chr16: 52,597,913-52,609,298 CASC16
    nsv7067642inversion1nstd229human GRCh38 chr16: 52,588,396-52,614,273 , GRCh37.p13 chr16: 52,622,308-52,648,185 CASC16, LOC105371265, 1 more genes
    nsv6996664copy number variation1nstd229human GRCh38 chr16: 52,597,169-52,642,316 , GRCh37.p13 chr16: 52,631,081-52,676,228 LINC03064, CASC16
    nsv6992640copy number variation1nstd229human GRCh38 chr16: 52,449,201-52,573,300 , GRCh37.p13 chr16: 52,483,113-52,607,212 TOX3, CASC16
    nsv6990835copy number variation1nstd229human GRCh38 chr16: 52,547,462-52,551,165 , GRCh37.p13 chr16: 52,581,374-52,585,077 CASC16, TOX3
    nsv6987743copy number variation1nstd229human GRCh38 chr16: 52,567,053-52,570,626 , GRCh37.p13 chr16: 52,600,965-52,604,538 CASC16
    nsv6978690copy number variation1nstd229human GRCh38 chr16: 52,594,838-53,045,838 , GRCh37.p13 chr16: 52,628,750-53,079,750 CHD9NB, MTCH2P4, 5 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6514980copy number variation1nstd223human GRCh38 chr16: 52,595,432-52,596,100 , GRCh37.p13 chr16: 52,629,344-52,630,012 CASC16
    nsv6507827copy number variation1nstd223human GRCh38 chr16: 52,570,596-52,571,821 , GRCh37.p13 chr16: 52,604,508-52,605,733 CASC16
    nsv6505523copy number variation1nstd223human GRCh38 chr16: 52,523,098-52,630,239 , GRCh37.p13 chr16: 52,557,010-52,664,151 TOX3, LOC105371265, 2 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6198562copy number variation1nstd214human GRCh38 chr16: 52,570,900-52,570,979 , GRCh37.p13 chr16: 52,604,812-52,604,891 CASC16
    nsv6145875copy number variation1nstd206human GRCh38 chr16: 52,529,072-52,984,736 , GRCh37.p13 chr16: 52,562,984-53,018,648 TOX3, LOC146253, 5 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6097968insertion1nstd212human GRCh38 chr16: 52,556,492-52,556,492 , GRCh37.p13 chr16: 52,590,404-52,590,404 CASC16
    nsv6095977insertion1nstd212human GRCh38 chr16: 52,558,276-52,558,276 , GRCh37.p13 chr16: 52,592,188-52,592,188 CASC16
    nsv6086757insertion1nstd212human GRCh38 chr16: 52,577,733-52,577,733 , GRCh37.p13 chr16: 52,611,645-52,611,645 CASC16
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