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Items: 1 to 20 of 147

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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
    nsv7077897inversion1nstd229human GRCh38 chr9: 130,525,097-130,577,350 , GRCh37.p13 chr9: 133,400,484-133,452,737 LOC100272217
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv6877565copy number variation1nstd229human GRCh38 chr9: 130,162,901-130,666,900 , GRCh37.p13 chr9: 133,223,061-133,542,287 MIR6856, LOC107987134, 9 more genes
    nsv6872488copy number variation1nstd229human GRCh38 chr9: 130,421,097-130,581,801 , GRCh37.p13 chr9: 133,296,484-133,457,188 LOC100272217, ASS1, 3 more genes
    nsv6871501copy number variation1nstd229human GRCh38 chr9: 130,542,248-130,576,078 , GRCh37.p13 chr9: 133,417,635-133,451,465 LOC100272217
    nsv6866968copy number variation1nstd229human GRCh38 chr9: 130,410,059-130,624,963 , GRCh37.p13 chr9: 133,285,446-133,500,350 LOC100272217, ASS1, 4 more genes
    nsv6866245copy number variation1nstd229human GRCh38 chr9: 130,519,512-130,592,637 , GRCh37.p13 chr9: 133,394,899-133,468,024 LOC100272217, FUBP3
    nsv6866083copy number variation1nstd229human GRCh38 chr9: 130,296,601-131,144,600 , GRCh37.p13 chr9: 133,223,061-134,019,987 ABL1, PRDM12, 17 more genes
    nsv6862977copy number variation1nstd229human GRCh38 chr9: 130,533,925-130,612,523 , GRCh37.p13 chr9: 133,409,312-133,487,910 LOC100272217, FUBP3
    nsv6858236copy number variation1nstd229human GRCh38 chr9: 130,576,321-130,576,355 , GRCh37.p13 chr9: 133,451,708-133,451,742 LOC100272217
    nsv6633348copy number variation1nstd224human GRCh37 chr9: 133,413,084-133,486,300 , GRCh38.p12 chr9: 130,537,697-130,610,913 LOC100272217, FUBP3
    nsv6455386copy number variation1nstd223human GRCh38 chr9: 130,173,101-130,938,500 , GRCh37.p13 chr9: 133,223,061-133,813,887 ABL1, PRDM12, 15 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
    nsv6313254copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,327,616-133,589,862 , GRCh38.p12 chr9: 130,452,229-130,714,475 ABL1, PRDM12, 6 more genes
    nsv6137445copy number variation1nstd213human GRCh37 chr9: 133,220,000-134,800,001 , GRCh38.p12 chr9: 130,347,674-131,924,614 ABL1, ASS1, 32 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
    nsv5317520copy number variation1nstd204human GRCh37.p13 chr9: 133,223,037-133,497,604 , GRCh38.p13 chr9: 130,177,410-130,622,217 , ASS1, 7 more genes
    nsv4845096copy number variation1nstd200human GRCh37 chr9: 132,939,713-133,497,581 , GRCh38.p12 chr9: 130,177,434-130,622,194 , FUBP3, 7 more genes
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