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Items: 1 to 20 of 219

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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
    nsv7097936copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,501,494-136,523,569 , GRCh38.p12 chr9: 133,636,372-133,658,447 DBH, DBH-AS1
    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
    nsv6897104copy number variation1nstd229human GRCh38 chr9: 133,657,330-133,661,308 , GRCh37.p13 chr9: 136,522,452-136,526,430 DBH, DBH-AS1, 1 more genes
    nsv6884502copy number variation1nstd229human GRCh38 chr9: 133,630,771-133,737,768 , GRCh37.p13 chr9: 136,495,893-136,602,890 SARDH, DBH-AS1, 1 more genes
    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
    nsv6009350copy number variation1nstd212human GRCh38 chr9: 133,657,460-133,657,514 , GRCh37.p13 chr9: 136,522,582-136,522,636 DBH, DBH-AS1
    nsv6002072copy number variation1nstd212human GRCh38 chr9: 133,657,414-133,657,478 , GRCh37.p13 chr9: 136,522,536-136,522,600 DBH, DBH-AS1
    nsv5306220copy number variation1nstd204human GRCh37.p13 chr9: 136,369,183-136,539,282 , GRCh38.p13 chr9: 133,488,438-133,674,160 , DBH, 6 more genes
    nsv5300644copy number variation1nstd204human GRCh38.p13 chr9: 133,603,597-133,677,947 , GRCh37.p13 chr9: 136,468,719-136,543,069 , SARDH, 3 more genes
    nsv5127821mobile element insertion1nstd203human GRCh38 chr9: 133,655,488-133,655,503 , GRCh37.p13 chr9: 136,520,610-136,520,625 DBH, DBH-AS1
    nsv4985822copy number variation1nstd200human GRCh38 chr9: 133,524,633-133,694,233 , GRCh37.p13 chr9: 136,389,755-136,559,355 , ADAMTSL2, 5 more genes
    nsv4847065copy number variation1nstd200human GRCh37 chr9: 136,468,729-136,543,067 , GRCh38.p12 chr9: 133,603,607-133,677,945 , DBH, 3 more genes
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