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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098066copy number variation4nstd102humanUncertain significance GRCh37 chr9: 135,139,626-140,034,216 , GRCh38.p12 chr9: 132,264,239-137,139,764 LINC02692, SNORD141A, 181 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
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6876743copy number variation1nstd229human GRCh38 chr9: 133,069,701-133,089,700 , GRCh37.p13 chr9: 135,945,088-135,965,087 CEL, CELP
    nsv6876413copy number variation1nstd229human GRCh38 chr9: 133,078,801-133,132,100 , GRCh37.p13 chr9: 135,954,188-136,007,487 CELP, RALGDS
    nsv6875622copy number variation1nstd229human GRCh38 chr9: 133,070,001-133,088,100 , GRCh37.p13 chr9: 135,945,388-135,963,487 CEL, CELP
    nsv6873117copy number variation1nstd229human GRCh38 chr9: 133,070,601-133,086,200 , GRCh37.p13 chr9: 135,945,988-135,961,587 CELP, CEL
    nsv6873047copy number variation1nstd229human GRCh38 chr9: 133,060,801-133,086,900 , GRCh37.p13 chr9: 135,936,188-135,962,287 CEL, CELP
    nsv6871899copy number variation1nstd229human GRCh38 chr9: 133,063,201-133,085,300 , GRCh37.p13 chr9: 135,938,588-135,960,687 CEL, CELP
    nsv6869510copy number variation1nstd229human GRCh38 chr9: 133,070,301-133,087,100 , GRCh37.p13 chr9: 135,945,688-135,962,487 CELP, CEL
    nsv6867242copy number variation1nstd229human GRCh38 chr9: 133,070,101-133,086,600 , GRCh37.p13 chr9: 135,945,488-135,961,987 CEL, CELP
    nsv6862705copy number variation1nstd229human GRCh38 chr9: 133,060,901-133,085,400 , GRCh37.p13 chr9: 135,936,288-135,960,787 CEL, CELP
    nsv6861602copy number variation1nstd229human GRCh38 chr9: 133,063,001-133,085,400 , GRCh37.p13 chr9: 135,938,388-135,960,787 CEL, CELP
    nsv6860876copy number variation1nstd229human GRCh38 chr9: 133,070,801-133,085,800 , GRCh37.p13 chr9: 135,946,188-135,961,187 CEL, CELP
    nsv6858261copy number variation1nstd229human GRCh38 chr9: 133,061,201-133,085,200 , GRCh37.p13 chr9: 135,936,588-135,960,587 CEL, CELP
    nsv6636049copy number variation1nstd102humanUncertain significance GRCh38 chr9: 133,061,658-133,086,400 , GRCh37.p13 chr9: 135,937,045-135,961,787 CEL, CELP
    nsv6635987copy number variation1nstd102humanUncertain significance GRCh38 chr9: 133,061,291-133,085,367 , GRCh37.p13 chr9: 135,936,678-135,960,754 CELP, CEL
    nsv6635372copy number variation3nstd227human GRCh38.p12 chr9: 133,071,778-133,082,065 , GRCh37 chr9: 135,947,165-135,957,452 CEL, CELP
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