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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954899insertion1nstd209human GRCh38 chr5: 152,397,012-152,397,012 , GRCh37.p13 chr5: 151,776,573-151,776,573 NMUR2
    nsv5543480insertion1nstd206human GRCh38 chr5: 152,403,752-152,403,768 , GRCh37.p13 chr5: 151,783,313-151,783,329 NMUR2
    nsv5087945mobile element insertion1nstd203human GRCh38 chr5: 152,397,012-152,397,031 , GRCh37.p13 chr5: 151,776,573-151,776,592 NMUR2
    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
    nsv4945211copy number variation1nstd200human GRCh38 chr5: 152,297,007-152,401,133 , GRCh37.p13 chr5: 151,676,568-151,780,694 NMUR2, LOC105378237, 1 more genes
    nsv4945209copy number variation1nstd200human GRCh38 chr5: 152,146,983-152,582,788 , GRCh37.p13 chr5: 151,526,544-151,962,349 NMUR2, RPL36AP20, 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
    nsv4824333copy number variation1nstd200human GRCh37 chr5: 151,676,568-151,780,694 , GRCh38.p12 chr5: 152,297,007-152,401,133 NMUR2, LOC105378236, 1 more genes
    nsv4729563copy number variation1nstd102humanUncertain significance GRCh37 chr5: 151,532,654-151,961,446 , GRCh38.p12 chr5: 152,153,093-152,581,885 NMUR2, LOC105378236, 3 more genes
    nsv4729407copy number variation1nstd102humanUncertain significance GRCh37 chr5: 151,718,918-152,279,323 , GRCh38.p12 chr5: 152,339,357-152,899,763 LINC01470, TRC-ACA1-1, 3 more genes
    nsv4674867copy number variation1nstd102humanUncertain significance GRCh37 chr5: 151,729,453-152,279,338 , GRCh38.p12 chr5: 152,349,892-152,899,778 LINC01470, NMUR2, 3 more genes
    nsv4545473insertion1nstd166human GRCh37.p13 chr5: 151,783,280-151,783,280 , GRCh38.p12 chr5: 152,403,719-152,403,719 NMUR2
    nsv4497888mobile element insertion1nstd166human GRCh37.p13 chr5: 151,783,671-151,783,671 , GRCh38.p12 chr5: 152,404,110-152,404,110 NMUR2
    nsv4478749mobile element insertion1nstd166human GRCh37.p13 chr5: 151,777,684-151,777,684 , GRCh38.p12 chr5: 152,398,123-152,398,123 NMUR2
    nsv4126445copy number variation1nstd166human GRCh37.p13 chr5: 151,782,578-151,797,652 , GRCh38.p12 chr5: 152,403,017-152,418,091 NMUR2
    nsv3923414copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811 HNRNPA3P7, RNU6-456P, 514 more genes
    nsv3921182copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758 RN7SKP148, TCOF1, 553 more genes
    nsv3914878copy number variation1nstd102humanPathogenic NCBI36 chr5: 146,520,648-163,194,778 , GRCh37.p13 chr5: 146,540,455-163,262,200 , GRCh38.p12 chr5: 147,160,892-163,835,194 LOC105378231, RN7SKP232, 247 more genes
    nsv3914009copy number variation1nstd102humanPathogenic NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106 UQCRQ, SNHG4, 489 more genes
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