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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892008copy number variation1nstd209human GRCh38 chr5: 141,480,504-141,482,778 , GRCh37.p13 chr5: 140,860,071-140,862,345 PCDHGC3, PCDHGA2, 19 more genes
    nsv5841161copy number variation1nstd209human GRCh38 chr5: 141,480,497-141,482,796 , GRCh37.p13 chr5: 140,860,064-140,862,363 PCDHGB5, PCDHGA7, 19 more genes
    nsv5638473insertion1nstd207human GRCh38 chr5: 141,508,683-141,508,683 , GRCh37.p13 chr5: 140,888,250-140,888,250 PCDHGA6, PCDHGA10, 21 more genes
    nsv5628287insertion1nstd207human GRCh38 chr5: 141,482,759-141,482,759 , GRCh37.p13 chr5: 140,862,326-140,862,326 PCDHGB5, PCDHGA1, 19 more genes
    nsv5554312sequence alteration1nstd206human GRCh38 chr5: 141,482,755-141,482,779 , GRCh37.p13 chr5: 140,862,322-140,862,346 PCDHGB1, PCDHGA9, 19 more genes
    nsv5547503insertion1nstd206human GRCh38 chr5: 141,482,755-141,482,755 , GRCh37.p13 chr5: 140,862,322-140,862,322 PCDHGA7, PCDHGA11, 19 more genes
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5378123translocation1nstd200human GRCh38 chr5: 141,480,504-141,480,504 , GRCh38 chr5: 141,482,779-141,482,779 , GRCh37.p13 chr5: 140,862,346-140,862,346 , GRCh37.p13 chr5: 140,860,071-140,860,071 PCDHGB4, PCDHGB3, 19 more genes
    nsv5340192translocation1nstd200human GRCh37 chr5: 140,860,071-140,860,071 , GRCh37 chr5: 140,862,346-140,862,346 , GRCh38.p12 chr5: 141,482,779-141,482,779 , GRCh38.p12 chr5: 141,480,504-141,480,504 PCDHGA1, PCDHGA8, 19 more genes
    nsv5320741translocation1nstd204human GRCh37.p13 chr5: 140,860,071-140,860,071 , GRCh37.p13 chr5: 140,862,346-140,862,346 , GRCh38.p13 chr5: 141,482,779-141,482,779 , GRCh38.p13 chr5: 141,480,504-141,480,504 PCDHGB4, PCDHGB3, 19 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4938948copy number variation1nstd200human GRCh38 chr5: 141,495,087-141,497,911 , GRCh37.p13 chr5: 140,874,654-140,877,478 PCDHGC3, PCDHGA11, 21 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4756334insertion1nstd199human GRCh37 chr5: 140,862,321-140,862,321 , GRCh38.p12 chr5: 141,482,754-141,482,754 PCDHGA9, PCDHGA5, 19 more genes
    nsv4590190copy number variation1nstd183human GRCh37 chr5: 140,868,116-140,909,299 , GRCh38.p12 chr5: 141,488,549-141,529,732 PCDHGB7, PCDHGA5, 22 more genes
    nsv4457090copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,424,333-148,985,999 , GRCh38.p12 chr5: 141,044,748-149,606,436 PCDHGC4, CKS1BP5, 165 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv4301572insertion1nstd166human GRCh37.p13 chr5: 140,888,111-140,888,111 , GRCh38.p12 chr5: 141,508,544-141,508,544 PCDHG@, PCDHGB4, 21 more genes
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