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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7074596inversion1nstd229human GRCh38 chr9: 129,481,040-129,487,922 , GRCh37.p13 chr9: 132,243,319-132,250,201 LINC00963
    nsv7068973inversion1nstd229human GRCh38 chr9: 129,470,380-129,658,423 , GRCh37.p13 chr9: 132,232,659-132,420,702 LINC00963, NTMT1, 3 more genes
    nsv7067401inversion1nstd229human GRCh38 chr9: 129,506,931-129,623,171 , GRCh37.p13 chr9: 132,269,210-132,385,450 NTMT1, LINC00963, 2 more genes
    nsv6876885copy number variation1nstd229human GRCh38 chr9: 129,489,619-129,495,030 , GRCh37.p13 chr9: 132,251,898-132,257,309 LINC00963
    nsv6875032copy number variation1nstd229human GRCh38 chr9: 129,508,468-129,521,253 , GRCh37.p13 chr9: 132,270,747-132,283,532 LINC00963
    nsv6873334copy number variation1nstd229human GRCh38 chr9: 129,484,162-129,486,746 , GRCh37.p13 chr9: 132,246,441-132,249,025 LINC00963
    nsv6868595copy number variation1nstd229human GRCh38 chr9: 129,339,601-129,648,300 , GRCh37.p13 chr9: 132,101,880-132,410,579 LOC105376291, C9orf50, 7 more genes
    nsv6867119copy number variation1nstd229human GRCh38 chr9: 129,502,044-129,511,341 , GRCh37.p13 chr9: 132,264,323-132,273,620 LINC00963
    nsv6865965copy number variation1nstd229human GRCh38 chr9: 129,489,580-129,494,990 , GRCh37.p13 chr9: 132,251,859-132,257,269 LINC00963
    nsv6861274copy number variation1nstd229human GRCh38 chr9: 129,510,637-129,519,026 , GRCh37.p13 chr9: 132,272,916-132,281,305 LINC00963
    nsv6860548copy number variation1nstd229human GRCh38 chr9: 129,485,701-129,489,600 , GRCh37.p13 chr9: 132,247,980-132,251,879 LINC00963
    nsv6633346copy number variation1nstd224human GRCh37 chr9: 132,254,665-132,321,716 , GRCh38.p12 chr9: 129,492,386-129,559,437 LINC00963
    nsv6452143copy number variation1nstd223human GRCh38 chr9: 129,492,313-129,495,256 , GRCh37.p13 chr9: 132,254,592-132,257,535 LINC00963
    nsv6447256copy number variation1nstd223human GRCh38 chr9: 129,483,666-129,733,968 , GRCh37.p13 chr9: 132,245,945-132,496,247 LINC00963, PRRX2, 5 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6137057copy number variation1nstd213human GRCh37 chr9: 130,360,000-135,460,001 , GRCh38.p12 chr9: 127,597,721-132,584,614 CRAT, GLE1, 145 more genes
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