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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5488606copy number variation1nstd206human GRCh38 chr9: 20,305,336-20,349,488 , GRCh37.p13 chr9: 20,305,334-20,349,486 SMNP, SLC24A2, 1 more genes
    nsv5040090inversion1nstd200human GRCh38 chr9: 12,646,715-21,082,031 , GRCh37.p13 chr9: 12,646,715-21,082,030 , RPS6, 98 more genes
    nsv4963581copy number variation1nstd200human GRCh38 chr9: 20,325,553-20,331,559 , GRCh37.p13 chr9: 20,325,551-20,331,557 SMNP
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4745683copy number variation1nstd199human GRCh37 chr9: 6,727,606-30,688,993 , GRCh38.p12 chr9: 6,727,606-30,688,995 , RPS6P10, 230 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4612868copy number variation1nstd183human GRCh37 chr9: 20,087,885-20,423,364 , GRCh38.p12 chr9: 20,087,887-20,423,366 MLLT3, RNU4-26P, 3 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4456028copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-38,472,979 , GRCh38.p12 chr9: 203,861-38,472,982 SNORA30B, LOC100419692, 559 more genes
    nsv4455615copy number variation1nstd102humanUncertain significance GRCh37 chr9: 20,323,068-20,457,595 , GRCh38.p12 chr9: 20,323,070-20,457,597 MLLT3, SMNP, 2 more genes
    nsv4455334copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,536,094-20,653,331 , GRCh38.p12 chr9: 19,536,096-20,653,332 GLRX3P1, LOC105375988, 9 more genes
    nsv4412138copy number variation1nstd174human GRCh37 chr9: 20,083,157-20,423,352 , GRCh38.p12 chr9: 20,083,159-20,423,354 MLLT3, SMNP, 3 more genes
    nsv4388503copy number variation1nstd173human GRCh37 chr9: 19,569,670-27,574,515 , GRCh38.p12 chr9: 19,569,672-27,574,517 , RMRPP5, 104 more genes
    nsv4367983copy number variation1nstd173human GRCh37 chr9: 19,544,082-20,653,480 , GRCh38.p12 chr9: 19,544,084-20,653,481 , RNU4-26P, 10 more genes
    nsv4350536copy number variation1nstd102humanPathogenic GRCh37 chr9: 214,309-39,156,958 , GRCh38.p12 chr9: 214,309-39,156,961 CSNK1G2P1, PAICSP1, 576 more genes
    nsv4185523copy number variation1nstd166human GRCh37.p13 chr9: 20,234,000-20,389,000 , GRCh38.p12 chr9: 20,234,002-20,389,002 MLLT3, SMNP, 1 more genes
    nsv3924377copy number variation1nstd102humanLikely benign GRCh38 chr9: 19,564,275-20,636,227 , GRCh37 chr9: 19,564,273-20,636,226 , NCBI36 chr9: 19,554,273-20,626,226 MIR4473, SLC24A2, 8 more genes
    nsv3923714copy number variation1nstd102humanPathogenic GRCh38 chr9: 193,412-70,630,731 , GRCh37 chr9: 220,253-73,245,647 , NCBI36 chr9: 210,253-72,435,467 LOC105379257, LOC105376002, 888 more genes
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