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Items: 1 to 20 of 373

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097553copy number variation1nstd102humanPathogenic GRCh37 chr5: 94,800,311-96,107,383 , GRCh38.p12 chr5: 95,464,607-96,771,679 LOC105379675, GPR150, 27 more genes
    nsv7058036inversion1nstd229human GRCh38 chr5: 94,195,543-97,660,538 , GRCh37.p13 chr5: 93,531,248-96,996,242 RIOK2, SPATA9, 51 more genes
    nsv7044198inversion1nstd229human GRCh38 chr5: 93,856,097-99,790,151 , GRCh37.p13 chr5: 93,191,803-99,125,855 FAM81B, LOC107986365, 78 more genes
    nsv6773004copy number variation1nstd229human GRCh38 chr5: 94,767,305-97,708,544 , GRCh37.p13 chr5: 94,103,010-97,044,248 FABP5P5, SPATA9, 45 more genes
    nsv6770732copy number variation1nstd229human GRCh38 chr5: 95,768,680-95,951,039 , GRCh37.p13 chr5: 95,104,384-95,286,743 LOC105379091, GLRX, 6 more genes
    nsv6768973copy number variation1nstd229human GRCh38 chr5: 95,952,872-96,356,331 , GRCh37.p13 chr5: 95,288,576-95,692,035 LOC107986365, MIR583, 7 more genes
    nsv6767202copy number variation1nstd229human GRCh38 chr5: 95,897,201-95,905,800 , GRCh37.p13 chr5: 95,232,905-95,241,504 ELL2
    nsv6767196copy number variation1nstd229human GRCh38 chr5: 95,464,994-96,106,661 , GRCh37.p13 chr5: 94,800,698-95,442,365 ELL2, ARSK, 19 more genes
    nsv6766430copy number variation1nstd229human GRCh38 chr5: 95,942,741-96,023,491 , GRCh37.p13 chr5: 95,278,445-95,359,195 FABP5P5, ELL2, 2 more genes
    nsv6761814copy number variation1nstd229human GRCh38 chr5: 95,883,289-95,885,615 , GRCh37.p13 chr5: 95,218,993-95,221,319 ELL2
    nsv6760011copy number variation1nstd229human GRCh38 chr5: 95,892,114-95,894,810 , GRCh37.p13 chr5: 95,227,818-95,230,514 ELL2
    nsv6630453copy number variation1nstd224human GRCh37 chr5: 95,072,623-95,423,944 , GRCh38.p12 chr5: 95,736,919-96,088,240 GLRX, LINC01554, 11 more genes
    nsv6574444inversion1nstd223human GRCh38 chr5: 95,893,464-95,894,246 , GRCh37.p13 chr5: 95,229,168-95,229,950 ELL2
    nsv6569676inversion1nstd223human GRCh38 chr5: 95,833,829-96,527,291 , GRCh37.p13 chr5: 95,169,533-95,862,995 MIR583HG, LOC105379675, 13 more genes
    nsv6410812copy number variation1nstd223human GRCh38 chr5: 95,381,684-95,927,497 , GRCh37.p13 chr5: 94,717,388-95,263,201 SKIC3, ARSK, 17 more genes
    nsv6405135copy number variation1nstd223human GRCh38 chr5: 95,768,680-95,951,039 , GRCh37.p13 chr5: 95,104,384-95,286,743 LOC105379091, LINC01554, 6 more genes
    nsv6403811copy number variation1nstd223human GRCh38 chr5: 95,952,872-96,356,331 , GRCh37.p13 chr5: 95,288,576-95,692,035 MIR583HG, ELL2, 7 more genes
    nsv6313721copy number variation1nstd102humanUncertain significance GRCh37 chr5: 95,240,864-95,630,972 , GRCh38.p12 chr5: 95,905,160-96,295,268 LOC101929710, LOC105379675, 6 more genes
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
    nsv6269263copy number variation1nstd214human GRCh38 chr5: 95,927,372-95,927,449 , GRCh37.p13 chr5: 95,263,076-95,263,153 ELL2
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