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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
    nsv5466659copy number variation1nstd206human GRCh38 chr5: 134,406,640-134,407,554 , GRCh37.p13 chr5: 133,742,331-133,743,245 CDKN2AIPNL
    nsv5300642copy number variation1nstd204human GRCh38.p13 chr5: 134,406,630-134,407,563 , GRCh37.p13 chr5: 133,742,321-133,743,254 CDKN2AIPNL
    nsv5090718mobile element insertion1nstd203human GRCh38 chr5: 134,403,488-134,403,503 , GRCh37.p13 chr5: 133,739,179-133,739,194 CDKN2AIPNL
    nsv5090241mobile element insertion1nstd203human GRCh38 chr5: 134,403,495-134,403,503 , GRCh37.p13 chr5: 133,739,186-133,739,194 CDKN2AIPNL
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 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
    nsv4938675copy number variation1nstd200human GRCh38 chr5: 134,401,030-134,402,283 , GRCh37.p13 chr5: 133,736,721-133,737,974 CDKN2AIPNL
    nsv4938673copy number variation1nstd200human GRCh38 chr5: 134,391,534-134,462,763 , GRCh37.p13 chr5: 133,727,225-133,798,454 , RPS10P11, 3 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4805838copy number variation1nstd200human GRCh37 chr5: 133,742,330-133,743,246 , GRCh38.p12 chr5: 134,406,639-134,407,555 CDKN2AIPNL
    nsv4804037copy number variation1nstd200human GRCh37 chr5: 133,736,720-133,737,974 , GRCh38.p12 chr5: 134,401,029-134,402,283 CDKN2AIPNL
    nsv4482636mobile element insertion1nstd166human GRCh37.p13 chr5: 133,739,179-133,739,179 , GRCh38.p12 chr5: 134,403,488-134,403,488 CDKN2AIPNL
    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
    nsv4116160copy number variation1nstd166human GRCh37.p13 chr5: 133,742,331-133,743,245 , GRCh38.p12 chr5: 134,406,640-134,407,554 CDKN2AIPNL
    nsv3971975copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 126,377,719-136,270,989 , GRCh38.p12 chr5: 127,042,027-136,935,300 ACTBP4, CAMLG, 157 more genes
    nsv3964351insertion1nstd168human GRCh38 chr5: 134,411,366-134,448,489 , GRCh37.p13 chr5: 133,747,057-133,784,180 , CDKN2AIPNL, 2 more genes
    nsv3924484copy number variation1nstd102humanPathogenic NCBI36 chr5: 132,894,824-134,211,267 , GRCh38 chr5: 133,531,234-134,847,678 , GRCh37 chr5: 132,866,925-134,183,368 C5orf24, UBE2B, 28 more genes
    nsv3923830copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,151,895-134,718,848 , GRCh38 chr5: 132,816,203-135,383,158 , NCBI36 chr5: 132,179,794-134,746,747 MTND5P11, TCF7, 60 more genes
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