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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077997inversion1nstd229human GRCh38 chr19: 50,085,764-53,270,581 , GRCh37.p13 chr19: 50,589,021-53,773,834 SNORD88B, ZNF320, 181 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7069681inversion1nstd229human GRCh38 chr19: 50,654,313-52,443,676 , GRCh37.p13 chr19: 51,157,570-52,946,929 CTU1, LOC100419835, 117 more genes
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 more genes
    nsv7013548copy number variation1nstd229human GRCh38 chr19: 51,463,369-51,511,271 , GRCh37.p13 chr19: 51,966,623-52,014,525 SIGLEC27P, SIGLEC12, 2 more genes
    nsv7011137copy number variation1nstd229human GRCh38 chr19: 51,491,121-51,493,572 , GRCh37.p13 chr19: 51,994,375-51,996,826 CEACAM18, SIGLEC12
    nsv7001045copy number variation1nstd229human GRCh38 chr19: 51,499,801-51,502,700 , GRCh37.p13 chr19: 52,003,055-52,005,954 SIGLEC12
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
    nsv6291759copy number variation1nstd102humanUncertain significance GRCh37 chr19: 51,769,834-52,415,762 , GRCh38.p12 chr19: 51,266,580-51,912,509 ZNF649-AS1, SIGLEC12, 46 more genes
    nsv6207624copy number variation1nstd214human GRCh38 chr19: 51,495,335-51,495,420 , GRCh37.p13 chr19: 51,998,589-51,998,674 SIGLEC12
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6041106copy number variation1nstd212human GRCh38 chr19: 51,489,180-51,489,428 , GRCh37.p13 chr19: 51,992,434-51,992,682 CEACAM18, SIGLEC12
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5594450copy number variation1nstd207human GRCh38 chr19: 51,495,202-51,495,253 , GRCh37.p13 chr19: 51,998,456-51,998,507 SIGLEC12
    nsv5517414copy number variation1nstd206human GRCh38 chr19: 51,489,186-51,489,428 , GRCh37.p13 chr19: 51,992,440-51,992,682 CEACAM18, SIGLEC12
    nsv5327285copy number variation1nstd204human GRCh37.p13 chr19: 51,992,414-51,992,707 , GRCh38.p13 chr19: 51,489,160-51,489,453 CEACAM18, SIGLEC12
    nsv5021105copy number variation1nstd200human GRCh38 chr19: 51,489,186-51,489,428 , GRCh37.p13 chr19: 51,992,440-51,992,682 SIGLEC12, CEACAM18
    nsv5021104copy number variation1nstd200human GRCh38 chr19: 51,488,206-51,492,291 , GRCh37.p13 chr19: 51,991,460-51,995,545 CEACAM18, SIGLEC12
    nsv4853434copy number variation1nstd200human GRCh37 chr19: 51,992,440-51,992,682 , GRCh38.p12 chr19: 51,489,186-51,489,428 CEACAM18, SIGLEC12
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
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