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Items: 1 to 20 of 194

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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
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 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
    nsv7060209inversion1nstd229human GRCh38 chr9: 133,220,670-135,537,297 , GRCh37.p13 chr9: 136,369,193-138,429,143 COL5A1, DBH, 66 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
    nsv6884853copy number variation1nstd229human GRCh38 chr9: 133,316,801-133,500,200 , GRCh37.p13 chr9|NW_003315925.1: 142,895-326,294 , GRCh37.p13 chr9: 136,183,638-136,365,322 SURF2, SURF6, 16 more genes
    nsv6882057copy number variation1nstd229human GRCh38 chr9: 133,316,601-133,495,400 , GRCh37.p13 chr9|NW_003315925.1: 142,695-321,494 , GRCh37.p13 chr9: 136,183,438-136,360,522 LCN1P2, SURF4, 16 more genes
    nsv6633673copy number variation1nstd224human GRCh37 chr9: 136,339,229-136,353,350 , GRCh38.p12 chr9: 133,474,107-133,488,228 , GRCh38.p12 chr9|NW_009646201.1: 300,201-314,322 SLC2A6
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6137060copy number variation1nstd213human GRCh37 chr9: 135,710,000-137,020,001 , GRCh38.p12 chr9: 132,834,613-134,154,879 CELP, SURF1, 47 more genes
    nsv5302705copy number variation1nstd204human GRCh38.p13 chr9: 133,471,848-133,472,954 , GRCh37.p13 chr9|NW_003315925.1: 297,942-299,048 , GRCh37.p13 chr9: 136,336,970-136,338,076 SLC2A6
    nsv4985819copy number variation1nstd200human GRCh38 chr9: 133,430,008-133,504,895 , GRCh37.p13 chr9|NW_003315925.1: 256,102-330,164 , GRCh37.p13 chr9: 136,295,128-136,369,192 SLC2A6, LOC102723855, 2 more genes
    nsv4683889copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,771,850-137,038,881 , GRCh38.p12 chr9: 132,896,463-134,173,759 GBGT1, CELP, 46 more genes
    nsv4681357copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,771,602-136,769,889 , GRCh38.p12 chr9: 132,896,215-133,904,767 ABO, GTF3C5, 40 more genes
    nsv4566038mobile element insertion1nstd166human GRCh37.p13 chr9: 136,339,853-136,339,853 , GRCh38.p12 chr9|NW_009646201.1: 300,825-300,825 , GRCh38.p12 chr9: 133,474,731-133,474,731 SLC2A6
    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
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