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Items: 1 to 20 of 508

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074768inversion1nstd229human GRCh38 chr9: 126,965,165-126,965,228 , GRCh37.p13 chr9: 129,727,444-129,727,507 RALGPS1
    nsv7074561inversion1nstd229human GRCh38 chr9: 127,184,126-127,189,146 , GRCh37.p13 chr9: 129,946,405-129,951,425 LOC105376278, RALGPS1
    nsv7072707inversion1nstd229human GRCh38 chr9: 127,185,492-127,188,705 , GRCh37.p13 chr9: 129,947,771-129,950,984 RALGPS1, LOC105376278
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv7068572inversion1nstd229human GRCh38 chr9: 127,189,145-127,189,732 , GRCh37.p13 chr9: 129,951,424-129,952,011 RALGPS1
    nsv7060023inversion1nstd229human GRCh38 chr9: 126,926,838-126,926,922 , GRCh37.p13 chr9: 129,689,117-129,689,201 RALGPS1
    nsv7058360inversion1nstd229human GRCh38 chr9: 127,017,383-127,017,414 , GRCh37.p13 chr9: 129,779,662-129,779,693 RALGPS1
    nsv6878043copy number variation1nstd229human GRCh38 chr9: 127,083,504-127,087,513 , GRCh37.p13 chr9: 129,845,783-129,849,792 RALGPS1, ANGPTL2
    nsv6877928copy number variation1nstd229human GRCh38 chr9: 126,960,744-126,960,786 , GRCh37.p13 chr9: 129,723,023-129,723,065 RALGPS1
    nsv6877717copy number variation1nstd229human GRCh38 chr9: 127,128,604-127,128,787 , GRCh37.p13 chr9: 129,890,883-129,891,066 RALGPS1
    nsv6876573copy number variation1nstd229human GRCh38 chr9: 127,199,945-127,331,688 , GRCh37.p13 chr9: 129,962,224-130,093,967 LOC100419923, RALGPS1, 1 more genes
    nsv6876114copy number variation1nstd229human GRCh38 chr9: 126,974,921-126,974,956 , GRCh37.p13 chr9: 129,737,200-129,737,235 RALGPS1
    nsv6874950copy number variation1nstd229human GRCh38 chr9: 126,948,501-126,959,800 , GRCh37.p13 chr9: 129,710,780-129,722,079 RALGPS1
    nsv6874901copy number variation1nstd229human GRCh38 chr9: 127,133,402-127,137,083 , GRCh37.p13 chr9: 129,895,681-129,899,362 RALGPS1
    nsv6874141copy number variation1nstd229human GRCh38 chr9: 127,123,401-127,137,800 , GRCh37.p13 chr9: 129,885,680-129,900,079 RALGPS1
    nsv6872967copy number variation1nstd229human GRCh38 chr9: 127,027,851-127,033,979 , GRCh37.p13 chr9: 129,790,130-129,796,258 RALGPS1
    nsv6871560copy number variation1nstd229human GRCh38 chr9: 127,080,534-127,084,678 , GRCh37.p13 chr9: 129,842,813-129,846,957 RALGPS1
    nsv6870631copy number variation1nstd229human GRCh38 chr9: 126,983,847-126,988,168 , GRCh37.p13 chr9: 129,746,126-129,750,447 RALGPS1
    nsv6870541copy number variation1nstd229human GRCh38 chr9: 127,215,557-127,229,484 , GRCh37.p13 chr9: 129,977,836-129,991,763 RALGPS1, GARNL3
    nsv6868942copy number variation1nstd229human GRCh38 chr9: 127,098,301-127,104,500 , GRCh37.p13 chr9: 129,860,580-129,866,779 RALGPS1, ANGPTL2
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