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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095657copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,011,002-45,213,778 , GRCh38.p12 chr19: 43,506,850-44,710,506 RN7SL368P, ZNF112, 52 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7015523copy number variation1nstd229human GRCh38 chr19: 43,562,771-43,577,075 , GRCh37.p13 chr19: 44,066,923-44,081,227 PINLYP, XRCC1
    nsv7014737copy number variation1nstd229human GRCh38 chr19: 43,559,820-43,683,290 , GRCh37.p13 chr19: 44,063,972-44,187,442 RN7SL368P, PLAUR, 8 more genes
    nsv7014573copy number variation1nstd229human GRCh38 chr19: 43,573,948-43,580,065 , GRCh37.p13 chr19: 44,078,100-44,084,217 XRCC1, PINLYP
    nsv7011811copy number variation1nstd229human GRCh38 chr19: 43,574,853-43,574,965 , GRCh37.p13 chr19: 44,079,005-44,079,117 XRCC1, PINLYP
    nsv7009619copy number variation1nstd229human GRCh38 chr19: 43,574,001-43,580,100 , GRCh37.p13 chr19: 44,078,153-44,084,252 PINLYP, XRCC1
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv6637474copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,084,067-44,096,910 , GRCh38.p12 chr19: 42,579,915-43,592,758 CEACAMP10, PRG1, 36 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6533267copy number variation1nstd223human GRCh38 chr19: 42,797,480-43,578,160 , GRCh37.p13 chr19: 43,301,632-44,082,312 , PSG1, 28 more genes
    nsv6530649copy number variation1nstd223human GRCh38 chr19: 42,576,896-43,593,497 , GRCh37.p13 chr19: 43,081,048-44,097,649 , PSG3, 37 more genes
    nsv6314086copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,082,847-44,100,076 , GRCh38.p12 chr19: 42,578,695-43,595,924 PSG9, PSG8-AS1, 37 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv5024694copy number variation1nstd200human GRCh38 chr19: 43,578,119-43,578,468 , GRCh37.p13 chr19: 44,082,271-44,082,620 PINLYP
    nsv5024672copy number variation1nstd200human GRCh38 chr19: 42,797,406-43,578,600 , GRCh37.p13 chr19: 43,301,558-44,082,752 , PINLYP, 28 more genes
    nsv4679272copy number variation1nstd189human GRCh37.p13 chr19: 43,906,705-44,198,705 , GRCh38.p12 chr19: 43,402,553-43,694,553 , PLAUR, 16 more genes
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