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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5641705insertion1nstd207human GRCh38 chr9: 137,050,136-137,050,136 , GRCh37.p13 chr9: 139,944,588-139,944,588 ENTPD2
    nsv5631058insertion1nstd207human GRCh38 chr9: 137,050,064-137,050,064 , GRCh37.p13 chr9: 139,944,516-139,944,516 ENTPD2
    nsv5629389insertion1nstd207human GRCh38 chr9: 137,050,200-137,050,200 , GRCh37.p13 chr9: 139,944,652-139,944,652 ENTPD2
    nsv5628259insertion1nstd207human GRCh38 chr9: 137,050,244-137,050,244 , GRCh37.p13 chr9: 139,944,696-139,944,696 ENTPD2
    nsv5487297copy number variation1nstd206human GRCh38 chr9: 137,047,169-137,047,936 , GRCh37.p13 chr9: 139,941,621-139,942,388 ENTPD2
    nsv5486068copy number variation1nstd206human GRCh38 chr9: 137,050,250-137,051,003 , GRCh37.p13 chr9: 139,944,702-139,945,455 ENTPD2, LOC105376327
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5381736copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,764,148-141,066,491 , GRCh38.p12 chr9: 136,869,696-138,172,039 PTGDS, LCN12, 63 more genes
    nsv5243007copy number variation1nstd204human GRCh38.p13 chr9: 136,845,001-137,273,000 , GRCh37.p13 chr9: 139,739,453-140,167,452 ENTPD2, LINC02908, 43 more genes
    nsv4973388copy number variation1nstd200human GRCh38 chr9: 137,047,169-137,047,936 , GRCh37.p13 chr9: 139,941,621-139,942,388 ENTPD2
    nsv4834139copy number variation1nstd200human GRCh37 chr9: 139,941,621-139,942,388 , GRCh38.p12 chr9: 137,047,169-137,047,936 ENTPD2
    nsv4768352copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532 MIR6722, EXD3, 108 more genes
    nsv4762603insertion1nstd199human GRCh37 chr9: 139,944,497-139,944,497 , GRCh38.p12 chr9: 137,050,045-137,050,045 ENTPD2
    nsv4734271copy number variation1nstd199human GRCh38.p12 chr9: 137,050,045-137,050,947 , GRCh37 chr9: 139,944,497-139,945,399 ENTPD2, LOC105376327
    nsv4728942copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,776,707-140,234,193 , GRCh38.p12 chr9: 136,882,255-137,339,741 GRIN1, CYSRT1, 42 more genes
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv4683252copy number variation2nstd102humanUncertain significance GRCh37 chr9: 138,594,085-140,062,314 , GRCh38.p12 chr9: 135,702,239-137,167,862 SAPCD2, MIR3621, 81 more genes
    nsv4681206copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,645,763-140,729,425 , GRCh38.p12 chr9: 135,753,917-137,834,973 DPP7, MIR4673, 112 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
    nsv4456509copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,766,260-140,186,072 , GRCh38.p12 chr9: 136,871,808-137,291,620 PAXX, CIMIP2A, 40 more genes
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