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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095288copy number variation1nstd102humanPathogenic GRCh37 chr19: 51,727,962-51,890,697 , GRCh38.p12 chr19: 51,224,706-51,387,443 LOC107985327, LIM2-AS1, 13 more genes
    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
    nsv7065725inversion1nstd229human GRCh38 chr19: 51,339,420-51,341,877 , GRCh37.p13 chr19: 51,842,674-51,845,131 VSIG10L
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 more genes
    nsv7062200inversion1nstd229human GRCh38 chr19: 51,156,828-51,481,685 , GRCh37.p13 chr19: 51,660,085-51,984,939 VSIG10L, SIGLEC20P, 27 more genes
    nsv7017906copy number variation1nstd229human GRCh38 chr19: 51,339,840-51,354,167 , GRCh37.p13 chr19: 51,843,094-51,857,421 ETFB, VSIG10L
    nsv7015937copy number variation1nstd229human GRCh38 chr19: 51,337,811-51,337,848 , GRCh37.p13 chr19: 51,841,065-51,841,102 VSIG10L
    nsv7013201copy number variation1nstd229human GRCh38 chr19: 51,334,401-51,369,100 , GRCh37.p13 chr19: 51,837,655-51,872,354 ETFB, VSIG10L, 1 more genes
    nsv7007949copy number variation1nstd229human GRCh38 chr19: 51,338,758-51,338,989 , GRCh37.p13 chr19: 51,842,012-51,842,243 VSIG10L
    nsv7002760copy number variation1nstd229human GRCh38 chr19: 51,330,735-51,344,415 , GRCh37.p13 chr19: 51,833,989-51,847,669 IGLON5, ETFB, 1 more genes
    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
    nsv6225721copy number variation1nstd214human GRCh38 chr19: 51,339,840-51,339,894 , GRCh37.p13 chr19: 51,843,094-51,843,148 VSIG10L
    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
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5946586copy number variation1nstd209human GRCh38 chr19: 51,339,840-51,339,894 , GRCh37.p13 chr19: 51,843,094-51,843,148 VSIG10L
    nsv5721873mobile element insertion2nstd211human GRCh38 chr19: 51,333,591-51,333,591 , GRCh37.p13 chr19: 51,836,845-51,836,845 VSIG10L
    nsv5699195mobile element insertion2nstd211human GRCh38 chr19: 51,333,668-51,333,668 , GRCh37.p13 chr19: 51,836,922-51,836,922 VSIG10L
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