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Items: 1 to 20 of 149

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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
    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
    nsv6793479copy number variation1nstd229human GRCh38 chr5: 132,765,786-132,771,130 , GRCh37.p13 chr5: 132,101,478-132,106,822 SEPTIN8
    nsv6792309copy number variation1nstd229human GRCh38 chr5: 132,777,101-132,778,000 , GRCh37.p13 chr5: 132,112,793-132,113,692 SEPTIN8
    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
    nsv6786929copy number variation1nstd229human GRCh38 chr5: 132,537,001-133,541,300 , GRCh37.p13 chr5: 131,872,693-132,876,991 ATP6V0E1P1, KIF3A, 27 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
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 TGFBI, RPS10P11, 110 more genes
    nsv6269806copy number variation1nstd214human GRCh38 chr5: 132,770,059-132,770,148 , GRCh37.p13 chr5: 132,105,751-132,105,840 SEPTIN8
    nsv6269059copy number variation1nstd214human GRCh38 chr5: 132,770,063-132,770,148 , GRCh37.p13 chr5: 132,105,755-132,105,840 SEPTIN8
    nsv6267892copy number variation1nstd214human GRCh38 chr5: 132,770,081-132,770,148 , GRCh37.p13 chr5: 132,105,773-132,105,840 SEPTIN8
    nsv6267273copy number variation1nstd214human GRCh38 chr5: 132,770,063-132,770,130 , GRCh37.p13 chr5: 132,105,755-132,105,822 SEPTIN8
    nsv6266426copy number variation1nstd214human GRCh38 chr5: 132,770,061-132,770,148 , GRCh37.p13 chr5: 132,105,753-132,105,840 SEPTIN8
    nsv6244854mobile element insertion1nstd215human GRCh38 chr5: 132,753,969-132,753,969 , GRCh37.p13 chr5: 132,089,661-132,089,661 CCNI2, SEPTIN8
    nsv6183920copy number variation1nstd214human GRCh38 chr5: 132,770,081-132,770,162 , GRCh37.p13 chr5: 132,105,773-132,105,854 SEPTIN8
    nsv6175667copy number variation1nstd214human GRCh38 chr5: 132,770,063-132,770,150 , GRCh37.p13 chr5: 132,105,755-132,105,842 SEPTIN8
    nsv6168028copy number variation1nstd214human GRCh38 chr5: 132,770,081-132,770,150 , GRCh37.p13 chr5: 132,105,773-132,105,842 SEPTIN8
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