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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673751copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,500,743-130,501,051 , GRCh38.p12 chr5: 131,165,050-131,165,358 HINT1
    nsv5307201copy number variation1nstd204human GRCh38.p13 chr5: 130,959,041-131,175,065 , GRCh37.p13 chr5: 130,294,734-130,510,758 RPL11P2, LYRM7, 3 more genes
    nsv5307085copy number variation1nstd204human GRCh38.p13 chr5: 131,148,321-131,179,929 , GRCh37.p13 chr5: 130,484,014-130,515,622 LYRM7, HINT1
    nsv5237221copy number variation1nstd204human GRCh38.p13 chr5: 131,148,692-131,163,099 , GRCh37.p13 chr5: 130,484,385-130,498,792 HINT1
    nsv5229426copy number variation1nstd204human GRCh38.p13 chr5: 130,960,501-131,179,600 , GRCh37.p13 chr5: 130,296,194-130,515,293 LOC402229, HINT1, 3 more genes
    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
    nsv4945064copy number variation1nstd200human GRCh38 chr5: 131,155,653-131,167,434 , GRCh37.p13 chr5: 130,491,346-130,503,127 HINT1
    nsv4945063copy number variation1nstd200human GRCh38 chr5: 131,148,538-131,179,861 , GRCh37.p13 chr5: 130,484,231-130,515,554 HINT1, LYRM7
    nsv4945062copy number variation1nstd200human GRCh38 chr5: 130,959,048-131,175,056 , GRCh37.p13 chr5: 130,294,741-130,510,749 LOC105379172, RPL11P2, 3 more genes
    nsv4945061copy number variation1nstd200human GRCh38 chr5: 130,925,316-131,352,346 , GRCh37.p13 chr5: 130,261,009-130,688,039 LYRM7, LOC402229, 4 more genes
    nsv4945060copy number variation1nstd200human GRCh38 chr5: 130,784,929-131,392,188 , GRCh37.p13 chr5: 130,120,622-130,727,881 HINT1, CDC42SE2, 6 more genes
    nsv4938556copy number variation1nstd200human GRCh38 chr5: 131,068,191-131,213,505 , GRCh37.p13 chr5: 130,403,884-130,549,198 HINT1, LOC105379172, 1 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4805828copy number variation1nstd200human GRCh37 chr5: 130,484,231-130,515,554 , GRCh38.p12 chr5: 131,148,538-131,179,861 HINT1, LYRM7
    nsv4805826copy number variation1nstd200human GRCh37 chr5: 130,294,741-130,510,749 , GRCh38.p12 chr5: 130,959,048-131,175,056 HINT1, LOC402229, 3 more genes
    nsv4805825copy number variation1nstd200human GRCh37 chr5: 130,120,622-130,727,881 , GRCh38.p12 chr5: 130,784,929-131,392,188 HINT1, RPL11P2, 6 more genes
    nsv4803960copy number variation1nstd200human GRCh37 chr5: 130,493,669-130,494,047 , GRCh38.p12 chr5: 131,157,976-131,158,354 HINT1
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