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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137085copy number variation1nstd102humanPathogenic GRCh37 chr5: 127,800,418-134,002,686 , GRCh38.p12 chr5: 128,464,725-134,666,996 CSF2, LOC402229, 99 more genes
    nsv7097506copy number variation1nstd102humanUncertain significance GRCh37 chr5: 131,726,362-131,729,964 , GRCh38.p12 chr5: 132,390,670-132,394,272 SLC22A5
    nsv7097505copy number variation1nstd102humanPathogenic GRCh37 chr5: 131,705,516-131,729,964 , GRCh38.p12 chr5: 132,369,824-132,394,272 MIR3936HG, SLC22A5
    nsv7093415delins1nstd102humanPathogenic GRCh37 chr5: 131,705,768-131,705,817 , GRCh38 chr5: 132,370,076-132,370,125 SLC22A5, MIR3936HG
    nsv7050047inversion1nstd229human GRCh38 chr5: 126,094,727-134,977,523 , GRCh37.p13 chr5: 125,430,420-134,313,213 RNU6-757P, SKP1, 145 more genes
    nsv7044234inversion1nstd229human GRCh38 chr5: 125,118,269-132,850,844 , GRCh37.p13 chr5: 124,453,962-132,186,536 RPLP1P7, IL4, 98 more genes
    nsv7042985inversion1nstd229human GRCh38 chr5: 129,885,016-134,639,437 , GRCh37.p13 chr5: 129,220,709-133,975,127 HSPA8P4, LINC02999, 85 more genes
    nsv7042749inversion1nstd229human GRCh38 chr5: 125,171,898-132,850,836 , GRCh37.p13 chr5: 124,507,591-132,186,528 LOC102723654, LOC105379174, 98 more genes
    nsv6789307copy number variation1nstd229human GRCh38 chr5: 132,386,739-132,390,096 , GRCh37.p13 chr5: 131,722,431-131,725,788 SLC22A5
    nsv6789266copy number variation1nstd229human GRCh38 chr5: 132,368,572-132,386,873 , GRCh37.p13 chr5: 131,704,264-131,722,565 SLC22A5, MIR3936HG
    nsv6788875copy number variation1nstd229human GRCh38 chr5: 132,371,034-132,371,085 , GRCh37.p13 chr5: 131,706,726-131,706,777 SLC22A5
    nsv6787056copy number variation1nstd229human GRCh38 chr5: 126,804,198-136,494,917 , GRCh37.p13 chr5: 126,139,890-135,830,606 SLC22A4, LOC105379199, 158 more genes
    nsv6785078copy number variation1nstd229human GRCh38 chr5: 132,266,001-132,504,200 , GRCh37.p13 chr5: 131,601,694-131,839,892 PDLIM4, SLC22A4, 6 more genes
    nsv6783481copy number variation1nstd229human GRCh38 chr5: 132,129,524-132,691,587 , GRCh37.p13 chr5: 131,465,217-132,027,279 MIR6830, SLC22A4, 16 more genes
    nsv6778158copy number variation1nstd229human GRCh38 chr5: 132,388,546-132,388,925 , GRCh37.p13 chr5: 131,724,238-131,724,617 SLC22A5
    nsv6630478copy number variation1nstd224human GRCh37 chr5: 131,694,077-131,705,667 , GRCh38.p12 chr5: 132,358,384-132,369,975 MIR3936, SLC22A5, 1 more genes
    nsv6568194inversion1nstd223human GRCh38 chr5: 125,171,897-132,850,837 , GRCh37.p13 chr5: 124,507,590-132,186,529 LOC105379199, LMNB1, 98 more genes
    nsv6413208copy number variation1nstd223human GRCh38 chr5: 132,369,401-132,369,900 , GRCh37.p13 chr5: 131,705,093-131,705,592 SLC22A5, MIR3936HG
    nsv6312173copy number variation1nstd102humanPathogenic GRCh37 chr5: 131,722,697-131,724,733 , GRCh38.p12 chr5: 132,387,005-132,389,041 SLC22A5
    nsv6311744copy number variation1nstd102humanPathogenic GRCh37 chr5: 131,713,846-131,720,003 , GRCh38.p12 chr5: 132,378,154-132,384,311 SLC22A5
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