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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv6916147copy number variation1nstd229human GRCh38 chr11: 130,866,175-130,866,243 , GRCh37.p13 chr11: 130,736,070-130,736,138 SNX19
    nsv6915416copy number variation1nstd229human GRCh38 chr11: 130,907,200-130,959,335 , GRCh37.p13 chr11: 130,777,095-130,829,230 SNX19
    nsv6911487copy number variation1nstd229human GRCh38 chr11: 130,553,739-131,533,260 , GRCh37.p13 chr11: 130,423,634-131,403,154 LOC105369579, LOC107984412, 15 more genes
    nsv6909840copy number variation1nstd229human GRCh38 chr11: 130,890,563-130,890,624 , GRCh37.p13 chr11: 130,760,458-130,760,519 SNX19
    nsv6906623copy number variation1nstd229human GRCh38 chr11: 130,896,282-131,017,157 , GRCh37.p13 chr11: 130,766,177-130,887,052 SNX19, RN7SL167P, 1 more genes
    nsv6906543copy number variation1nstd229human GRCh38 chr11: 130,899,554-130,900,067 , GRCh37.p13 chr11: 130,769,449-130,769,962 SNX19
    nsv6905918copy number variation1nstd229human GRCh38 chr11: 130,720,239-131,215,051 , GRCh37.p13 chr11: 130,590,134-131,084,946 LOC105369575, PPP1R10P1, 9 more genes
    nsv6904413copy number variation1nstd229human GRCh38 chr11: 130,829,756-130,947,650 , GRCh37.p13 chr11: 130,699,651-130,817,545 LINC02551, SNX19
    nsv6901253copy number variation1nstd229human GRCh38 chr11: 130,912,508-130,923,215 , GRCh37.p13 chr11: 130,782,403-130,793,110 SNX19
    nsv6900553copy number variation1nstd229human GRCh38 chr11: 130,868,932-130,876,728 , GRCh37.p13 chr11: 130,738,827-130,746,623 SNX19
    nsv6898160copy number variation1nstd229human GRCh38 chr11: 130,911,812-130,912,061 , GRCh37.p13 chr11: 130,781,707-130,781,956 SNX19
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6634467copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 127,074,235-135,006,516 , GRCh38.p12 chr11: 127,204,340-135,076,622 APLP2, BAK1P2, 98 more genes
    nsv6620889copy number variation2nstd224human GRCh37 chr11: 130,779,410-130,878,093 , GRCh38.p12 chr11: 130,909,515-131,008,198 SNX19, RN7SL167P, 1 more genes
    nsv6474765copy number variation1nstd223human GRCh38 chr11: 130,904,891-130,907,098 , GRCh37.p13 chr11: 130,774,786-130,776,993 SNX19
    nsv6474371copy number variation1nstd223human GRCh38 chr11: 130,868,105-130,868,482 , GRCh37.p13 chr11: 130,738,000-130,738,377 SNX19
    nsv6472049copy number variation1nstd223human GRCh38 chr11: 130,896,282-131,017,149 , GRCh37.p13 chr11: 130,766,177-130,887,044 RN7SL167P, SNX19, 1 more genes
    nsv6471611copy number variation1nstd223human GRCh38 chr11: 130,914,672-130,921,434 , GRCh37.p13 chr11: 130,784,567-130,791,329 SNX19
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