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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7070239inversion1nstd229human GRCh38 chr9: 128,869,438-129,153,886 , GRCh37.p13 chr9: 131,631,717-131,916,165 DOLK, PTPA, 10 more genes
    nsv7067104inversion1nstd229human GRCh38 chr9: 129,090,075-129,091,449 , GRCh37.p13 chr9: 131,852,354-131,853,728 DOLPP1
    nsv6869404copy number variation1nstd229human GRCh38 chr9: 129,088,777-129,088,968 , GRCh37.p13 chr9: 131,851,056-131,851,247 DOLPP1
    nsv6858457copy number variation1nstd229human GRCh38 chr9: 129,090,585-129,094,181 , GRCh37.p13 chr9: 131,852,864-131,856,460 CRAT, DOLPP1
    nsv6447911copy number variation1nstd223human GRCh38 chr9: 129,076,901-129,079,600 , GRCh37.p13 chr9: 131,839,180-131,841,879 DOLPP1
    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
    nsv6142156copy number variation1nstd206human GRCh38 chr9: 129,036,552-129,154,552 , GRCh37.p13 chr9: 131,798,831-131,916,831 CRAT, DOLPP1, 2 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
    nsv5475275copy number variation1nstd206human GRCh38 chr9: 129,078,228-129,079,715 , GRCh37.p13 chr9: 131,840,507-131,841,994 DOLPP1
    nsv5316007copy number variation1nstd204human GRCh38.p13 chr9: 129,090,921-129,092,611 , GRCh37.p13 chr9: 131,853,200-131,854,890 DOLPP1
    nsv5244619copy number variation1nstd204human GRCh38.p13 chr9: 129,090,901-129,092,600 , GRCh37.p13 chr9: 131,853,180-131,854,879 DOLPP1
    nsv5241889copy number variation1nstd204human GRCh38.p13 chr9: 128,441,101-129,240,100 , GRCh37.p13 chr9: 131,203,380-132,002,379 , KYAT1, 32 more genes
    nsv4675731copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,957,344-132,310,210 , GRCh38.p12 chr9: 128,195,065-129,547,931 PTPA, GLE1, 55 more genes
    nsv4675555copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,094,304-131,863,858 , GRCh38.p12 chr9: 128,332,025-129,101,579 ENDOG, SPOUT1, 35 more genes
    nsv4599544copy number variation1nstd183human GRCh37 chr9: 131,804,785-131,849,036 , GRCh38.p12 chr9: 129,042,506-129,086,757 DOLPP1, MIGA2
    nsv4558919mobile element insertion1nstd166human GRCh37.p13 chr9: 131,849,416-131,849,416 , GRCh38.p12 chr9: 129,087,137-129,087,137 DOLPP1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
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