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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5036269inversion1nstd200human GRCh38 chr9: 79,108,237-87,224,469 , GRCh37.p13 chr9: 81,723,153-89,839,384 , RMI1, 100 more genes
    nsv4608464copy number variation1nstd183human GRCh37 chr9: 89,560,746-89,562,196 , GRCh38.p12 chr9: 86,945,831-86,947,281 GAS1, GAS1RR
    nsv4603611copy number variation1nstd183human GRCh37 chr9: 89,559,235-89,559,489 , GRCh38.p12 chr9: 86,944,320-86,944,574 GAS1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4420294copy number variation1nstd174human GRCh37 chr9: 89,560,746-89,562,196 , GRCh38.p12 chr9: 86,945,831-86,947,281 GAS1RR, GAS1
    nsv4349215copy number variation1nstd102humanPathogenic GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992 SPATA31C1, LINC02893, 280 more genes
    nsv4314197inversion1nstd166human GRCh37.p13 chr9: 88,968,744-90,042,303 , GRCh38.p12 chr9: 86,353,829-87,427,388 , TUT7, 14 more genes
    nsv4188164copy number variation1nstd166human GRCh37.p13 chr9: 89,392,872-89,568,934 , GRCh38.p12 chr9: 86,777,957-86,954,019 GAS1RR, GAS1
    nsv3964768copy number variation1nstd168human GRCh38 chr9: 86,899,035-87,015,437 , GRCh37.p13 chr9: 89,513,950-89,630,352 GAS1RR, GAS1, 2 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
    nsv3919257copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718 LOC107987031, LOC105376234, 2169 more genes
    nsv3917022copy number variation1nstd102humanPathogenic GRCh37 chr9: 214,367-141,008,915 , GRCh38 chr9: 193,412-138,114,463 , NCBI36 chr9: 204,367-140,128,736 RN7SKP87, SPATA6L, 2168 more genes
    nsv3915973copy number variation2nstd102humanPathogenic GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346 CTNNAL1, QSOX2, 2170 more genes
    nsv3915533copy number variation1nstd102humanPathogenic GRCh37 chr9: 88,694,766-94,589,503 , NCBI36 chr9: 87,884,586-93,629,324 , GRCh38 chr9: 86,079,851-91,827,221 SPIN1, PAICSP2, 98 more genes
    nsv3914702copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,130,848-109,341,774 , NCBI36 chr9: 70,225,166-108,381,595 , GRCh38 chr9: 68,420,430-106,579,493 CDCA7P2, ASPN, 603 more genes
    nsv3912247copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981 ALOX15P2, LOC107987061, 2184 more genes
    nsv3911702copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-88,130,444 , NCBI36 chr9: 193,861-89,935,179 , GRCh37 chr9: 203,861-90,745,359 ATP8B5P, RPS26P2, 1113 more genes
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