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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7014206copy number variation1nstd229human GRCh38 chr19: 9,088,780-9,099,720 , GRCh37.p13 chr19: 9,199,456-9,210,396 OR1M1
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv7010921copy number variation1nstd229human GRCh38 chr19: 9,086,888-9,091,651 , GRCh37.p13 chr19: 9,197,564-9,202,327 OR1M1
    nsv7009964copy number variation1nstd229human GRCh38 chr19: 9,094,484-9,095,397 , GRCh37.p13 chr19: 9,205,160-9,206,073 OR1M1
    nsv6999921copy number variation1nstd229human GRCh38 chr19: 9,082,322-9,128,751 , GRCh37.p13 chr19: 9,192,998-9,239,427 OR1M4P, OR7G1, 4 more genes
    nsv6999324copy number variation1nstd229human GRCh38 chr19: 9,090,101-9,094,300 , GRCh37.p13 chr19: 9,200,777-9,204,976 OR1M1
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5936250copy number variation1nstd209human GRCh38 chr19: 8,931,524-9,173,686 , GRCh37.p13 chr19: 9,042,200-9,284,362 ZNF317, OR7G1, 8 more genes
    nsv5299893copy number variation1nstd204human GRCh37.p13 chr19: 9,137,377-9,230,976 , GRCh38.p13 chr19: 9,026,701-9,120,300 OR7G1, OR1M1, 4 more genes
    nsv4864904copy number variation1nstd200human GRCh37 chr19: 9,128,772-9,210,441 , GRCh38.p12 chr19: 9,018,096-9,099,765 OR1M1, OR1M4P, 2 more genes
    nsv4729804copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,680,063-9,273,676 , GRCh38.p12 chr19: 8,615,177-9,163,000 OR7G1, OR7G2, 14 more genes
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
    nsv4679423copy number variation1nstd189human GRCh37.p13 chr19: 9,040,762-9,213,105 , GRCh38.p12 chr19: 8,930,086-9,102,429 MUC16, OR1M1, 4 more genes
    nsv4679349copy number variation1nstd189human GRCh37.p13 chr19: 9,063,112-9,252,527 , GRCh38.p12 chr19: 8,952,436-9,141,851 ZNF317, MUC16, 8 more genes
    nsv4436244complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 8,891,157-9,974,378 , GRCh37 chr19: 9,001,833-10,085,054 PIN1, UBE2L4, 51 more genes
    nsv4269019copy number variation1nstd166human GRCh37.p13 chr19: 8,799,185-9,251,695 , GRCh38.p12 chr19: 8,688,936-9,141,019 OR7G15P, OR7G1, 13 more genes
    nsv4267120copy number variation1nstd166human GRCh37.p13 chr19: 9,200,736-9,204,963 , GRCh38.p12 chr19: 9,090,060-9,094,287 OR1M1
    nsv3966545copy number variation1nstd168human GRCh38 chr19: 9,043,066-9,181,783 , GRCh37.p13 chr19: 9,153,742-9,292,459 ZNF317, OR7G1, 6 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
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