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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098902copy number variation1nstd102humanPathogenic GRCh37 chr16: 86,544,176-88,110,267 , GRCh38.p12 chr16: 86,510,570-88,076,661 LOC107984816, BANP, 33 more genes
    nsv7074636inversion1nstd229human GRCh38 chr16: 87,250,982-87,400,876 , GRCh37.p13 chr16: 87,284,588-87,434,482 LOC101928682, FBXO31, 5 more genes
    nsv7071774inversion1nstd229human GRCh38 chr16: 87,400,685-87,403,136 , GRCh37.p13 chr16: 87,434,291-87,436,742 MAP1LC3B
    nsv6994926copy number variation1nstd229human GRCh38 chr16: 87,391,472-87,403,284 , GRCh37.p13 chr16: 87,425,078-87,436,890 MAP1LC3B, FBXO31
    nsv6989937copy number variation1nstd229human GRCh38 chr16: 87,384,003-87,399,447 , GRCh37.p13 chr16: 87,417,609-87,433,053 MAP1LC3B, FBXO31, 1 more genes
    nsv6986156copy number variation1nstd229human GRCh38 chr16: 87,393,171-87,396,512 , GRCh37.p13 chr16: 87,426,777-87,430,118 MAP1LC3B
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6504059copy number variation1nstd223human GRCh38 chr16: 87,391,601-87,394,300 , GRCh37.p13 chr16: 87,425,207-87,427,906 MAP1LC3B, FBXO31
    nsv6499560copy number variation1nstd223human GRCh38 chr16: 87,396,001-87,397,400 , GRCh37.p13 chr16: 87,429,607-87,431,006 MAP1LC3B
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
    nsv6289897copy number variation1nstd102humanPathogenic GRCh37 chr16: 86,243,180-87,703,229 , GRCh38.p12 chr16: 86,209,574-87,669,623 LINC02135, FOXF1, 28 more genes
    nsv6133214copy number variation1nstd213human GRCh37 chr16: 85,100,000-90,290,001 , GRCh38.p12 chr16: 85,066,394-90,223,593 AFG3L1P, APRT, 156 more genes
    nsv6133210copy number variation1nstd213human GRCh37 chr16: 78,970,000-88,180,001 , GRCh38.p12 chr16: 78,936,103-88,146,395 , CA5A, 152 more genes
    nsv6133036copy number variation1nstd213human GRCh37 chr16: 85,940,000-90,290,001 , GRCh38.p12 chr16: 85,906,394-90,223,593 AFG3L1P, APRT, 134 more genes
    nsv6133005copy number variation1nstd213human GRCh37 chr16: 86,880,000-88,190,001 , GRCh38.p12 chr16: 86,846,394-88,156,395 CA5A, NR3C1P1, 23 more genes
    nsv5944579copy number variation1nstd209human GRCh38 chr16: 87,392,558-87,392,649 , GRCh37.p13 chr16: 87,426,164-87,426,255 FBXO31, MAP1LC3B
    nsv5710479mobile element insertion2nstd211human GRCh38 chr16: 87,393,706-87,393,706 , GRCh37.p13 chr16: 87,427,312-87,427,312 MAP1LC3B
    nsv5530238copy number variation1nstd206human GRCh38 chr16: 87,381,977-87,392,328 , GRCh37.p13 chr16: 87,415,583-87,425,934 FBXO31, MAP1LC3B, 1 more genes
    nsv5522094copy number variation1nstd206human GRCh38 chr16: 87,400,234-87,401,898 , GRCh37.p13 chr16: 87,433,840-87,435,504 MAP1LC3B
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