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Items: 1 to 20 of 92

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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
    nsv7062200inversion1nstd229human GRCh38 chr19: 51,156,828-51,481,685 , GRCh37.p13 chr19: 51,660,085-51,984,939 VSIG10L, SIGLEC20P, 27 more genes
    nsv7016759copy number variation1nstd229human GRCh38 chr19: 51,454,022-51,457,638 , GRCh37.p13 chr19: 51,957,276-51,960,892 SIGLEC8
    nsv7016528copy number variation1nstd229human GRCh38 chr19: 51,413,374-51,467,958 , GRCh37.p13 chr19: 51,916,628-51,971,212 SIGLEC10-AS1, SIGLEC10, 3 more genes
    nsv7005083copy number variation1nstd229human GRCh38 chr19: 51,419,771-51,473,802 , GRCh37.p13 chr19: 51,923,025-51,977,056 SIGLEC8, SIGLEC26P, 1 more genes
    nsv7004686copy number variation1nstd229human GRCh38 chr19: 51,392,291-51,451,684 , GRCh37.p13 chr19: 51,895,545-51,954,938 SIGLEC10-AS1, SIGLEC8, 3 more genes
    nsv6529326copy number variation1nstd223human GRCh38 chr19: 51,419,771-51,473,801 , GRCh37.p13 chr19: 51,923,025-51,977,055 SIGLEC26P, SIGLEC8, 1 more genes
    nsv6522821copy number variation1nstd223human GRCh38 chr19: 51,392,290-51,451,683 , GRCh37.p13 chr19: 51,895,544-51,954,937 SIGLEC10, SIGLEC10-AS1, 3 more genes
    nsv6520788copy number variation1nstd223human GRCh38 chr19: 51,434,379-51,452,482 , GRCh37.p13 chr19: 51,937,633-51,955,736 SIGLEC8
    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
    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
    nsv5946088copy number variation1nstd209human GRCh38 chr19: 51,419,771-51,473,800 , GRCh37.p13 chr19: 51,923,025-51,977,054 SIGLEC25P, SIGLEC8, 1 more genes
    nsv4865277copy number variation1nstd200human GRCh37 chr19: 51,923,025-51,977,056 , GRCh38.p12 chr19: 51,419,771-51,473,802 SIGLEC26P, SIGLEC8, 1 more genes
    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
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
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