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Items: 1 to 20 of 102

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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
    nsv7012282copy number variation1nstd229human GRCh38 chr19: 51,117,410-51,135,253 , GRCh37.p13 chr19: 51,620,667-51,638,510 SIGLEC18P, SIGLEC9
    nsv7002900copy number variation1nstd229human GRCh38 chr19: 51,115,581-51,126,726 , GRCh37.p13 chr19: 51,618,838-51,629,983 SIGLEC9, SIGLEC18P
    nsv6637793copy number variation1nstd102humanUncertain significance GRCh37 chr19: 51,623,330-51,694,022 , GRCh38.p12 chr19: 51,120,073-51,190,766 SIGLEC9, SIGLEC20P, 4 more genes
    nsv6525034copy number variation1nstd223human GRCh38 chr19: 51,123,901-51,125,600 , GRCh37.p13 chr19: 51,627,158-51,628,857 SIGLEC9
    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
    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
    nsv5529591copy number variation1nstd206human GRCh38 chr19: 51,129,285-51,129,652 , GRCh37.p13 chr19: 51,632,542-51,632,909 SIGLEC9
    nsv5321632copy number variation1nstd204human GRCh37.p13 chr19: 51,615,064-51,637,006 , GRCh38.p13 chr19: 51,111,807-51,133,749 SIGLEC9, SIGLEC18P
    nsv5294116copy number variation1nstd204human GRCh38.p13 chr19: 51,127,938-51,128,937 , GRCh37.p13 chr19: 51,631,195-51,632,194 SIGLEC9
    nsv5287160copy number variation1nstd204human GRCh38.p13 chr19: 51,118,094-51,132,076 , GRCh37.p13 chr19: 51,621,351-51,635,333 SIGLEC9, SIGLEC18P
    nsv5283592copy number variation1nstd204human GRCh38.p13 chr19: 51,111,594-51,133,554 , GRCh37.p13 chr19: 51,614,851-51,636,811 SIGLEC18P, SIGLEC9
    nsv5187393mobile element insertion1nstd203human GRCh38 chr19: 51,133,640-51,133,656 , GRCh37.p13 chr19: 51,636,897-51,636,913 SIGLEC9
    nsv5175259mobile element insertion1nstd203human GRCh38 chr19: 51,129,140-51,129,176 , GRCh37.p13 chr19: 51,632,397-51,632,433 SIGLEC9
    nsv5021095copy number variation1nstd200human GRCh38 chr19: 51,124,736-51,142,082 , GRCh37.p13 chr19: 51,627,993-51,645,339 SIGLEC7, SIGLEC9
    nsv4853428copy number variation1nstd200human GRCh37 chr19: 51,627,993-51,645,339 , GRCh38.p12 chr19: 51,124,736-51,142,082 SIGLEC9, SIGLEC7
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