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Items: 1 to 20 of 710

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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
    nsv7058007inversion1nstd229human GRCh38 chr5: 130,124,307-130,131,762 , GRCh37.p13 chr5: 129,460,000-129,467,455 CHSY3
    nsv7055992inversion1nstd229human GRCh38 chr5: 130,079,724-130,079,747 , GRCh37.p13 chr5: 129,415,417-129,415,440 CHSY3
    nsv7053417inversion1nstd229human GRCh38 chr5: 130,071,706-130,084,783 , GRCh37.p13 chr5: 129,407,399-129,420,476 CHSY3
    nsv7052077inversion1nstd229human GRCh38 chr5: 130,071,707-130,077,885 , GRCh37.p13 chr5: 129,407,400-129,413,578 CHSY3
    nsv7050263inversion1nstd229human GRCh38 chr5: 126,655,648-130,498,485 , GRCh37.p13 chr5: 125,991,340-129,834,178 RNA5SP191, LMNB1, 42 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
    nsv7049526inversion1nstd229human GRCh38 chr5: 130,131,604-130,141,501 , GRCh37.p13 chr5: 129,467,297-129,477,194 HSPA8P4, CHSY3
    nsv7048422inversion1nstd229human GRCh38 chr5: 129,943,437-129,943,480 , GRCh37.p13 chr5: 129,279,130-129,279,173 CHSY3
    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
    nsv6798031copy number variation1nstd229human GRCh38 chr5: 129,876,101-129,948,900 , GRCh37.p13 chr5: 129,211,794-129,284,593 LOC112267944, CHSY3
    nsv6797728copy number variation1nstd229human GRCh38 chr5: 129,916,522-129,916,673 , GRCh37.p13 chr5: 129,252,215-129,252,366 CHSY3
    nsv6797711copy number variation1nstd229human GRCh38 chr5: 130,173,893-130,174,742 , GRCh37.p13 chr5: 129,509,586-129,510,435 CHSY3
    nsv6797596copy number variation1nstd229human GRCh38 chr5: 130,136,502-130,136,532 , GRCh37.p13 chr5: 129,472,195-129,472,225 CHSY3
    nsv6797147copy number variation1nstd229human GRCh38 chr5: 129,998,555-130,006,822 , GRCh37.p13 chr5: 129,334,248-129,342,515 CHSY3
    nsv6797132copy number variation1nstd229human GRCh38 chr5: 130,171,742-130,172,236 , GRCh37.p13 chr5: 129,507,435-129,507,929 CHSY3
    nsv6796971copy number variation1nstd229human GRCh38 chr5: 130,032,480-130,032,855 , GRCh37.p13 chr5: 129,368,173-129,368,548 CHSY3
    nsv6796245copy number variation1nstd229human GRCh38 chr5: 130,162,563-130,163,013 , GRCh37.p13 chr5: 129,498,256-129,498,706 CHSY3
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