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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148265copy number variation1nstd102humanPathogenic GRCh38 chr5: 176,447,531-177,312,407 , GRCh37.p13 chr5: 175,874,532-176,739,408 MXD3, FAF2, 19 more genes
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7050002inversion1nstd229human GRCh38 chr5: 175,906,338-177,936,522 , GRCh37.p13 chr5: 175,333,341-177,363,523 PRR7, OR1X5P, 60 more genes
    nsv7041901inversion1nstd229human GRCh38 chr5: 175,920,087-179,128,938 , GRCh37.p13 chr5: 175,347,090-178,555,939 LOC100288803, NHP2, 98 more genes
    nsv7040659inversion1nstd229human GRCh38 chr5: 174,927,732-178,443,561 , GRCh37.p13 chr5: 174,354,735-177,870,562 RN7SKP148, FAM193B-DT, 90 more genes
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6793057copy number variation1nstd229human GRCh38 chr5: 176,624,975-176,860,934 , GRCh37.p13 chr5: 176,051,976-176,287,935 MIR4281, EIF4E1B, 4 more genes
    nsv6782160copy number variation1nstd229human GRCh38 chr5: 176,616,290-176,856,593 , GRCh37.p13 chr5: 176,043,291-176,283,594 MIR4281, LINC01574, 4 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6315318copy number variation1nstd102humanPathogenic GRCh38 chr5: 176,449,583-177,376,826 , GRCh37.p13 chr5: 175,876,584-176,803,827 FAF2, FGFR4, 22 more genes
    nsv6312189copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,047,812-177,422,934 , GRCh38.p12 chr5: 176,620,811-177,995,933 PFN3, UIMC1, 42 more genes
    nsv6291140copy number variation1nstd102humanUncertain significance GRCh37 chr5: 175,668,563-176,182,615 , GRCh38.p12 chr5: 176,241,560-176,755,614 MIR4281, HIGD2A, 16 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135133copy number variation1nstd213human GRCh37 chr5: 175,930,000-176,340,001 , GRCh38.p12 chr5: 176,502,999-176,913,000 HK3, MIR4281, 11 more genes
    nsv6112170inversion1nstd212human GRCh38 chr5: 175,902,456-177,920,039 , GRCh37.p13 chr5: 175,329,459-177,347,040 , CLTB, 65 more genes
    nsv6102110inversion1nstd212human GRCh38 chr5: 176,282,586-177,635,732 , GRCh37.p13 chr5: 175,709,589-177,062,733 , CLTB, 46 more genes
    nsv5977326inversion1nstd209human GRCh38 chr5: 176,286,704-177,635,736 , GRCh37.p13 chr5: 175,713,707-177,062,737 , CLTB, 46 more genes
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5890062copy number variation1nstd209human GRCh38 chr5: 176,061,658-178,007,127 , GRCh37.p13 chr5: 175,488,661-177,434,128 , DBN1, 65 more genes
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