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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
    nsv7141342insertion1nstd232human GRCh37.p13 chr9: 136,200,651-136,200,651 , GRCh38.p12 chr9: 133,333,815-133,333,815 , GRCh38.p12 chr9|NW_009646201.1: 159,909-159,909 SURF6
    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
    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
    nsv6886440copy number variation1nstd229human GRCh38 chr9: 133,325,716-133,332,148 , GRCh37.p13 chr9: 136,192,553-136,198,984 , GRCh37.p13 chr9|NW_003315925.1: 151,810-158,242 SURF6
    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
    nsv6882761copy number variation1nstd229human GRCh38 chr9: 133,328,883-133,331,829 , GRCh37.p13 chr9|NW_003315925.1: 154,977-157,923 , GRCh37.p13 chr9: 136,195,719-136,198,665 SURF6
    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
    nsv6881766copy number variation1nstd229human GRCh38 chr9: 133,331,053-133,344,789 , GRCh37.p13 chr9|NW_003315925.1: 157,147-170,883 , GRCh37.p13 chr9: 136,197,889-136,211,644 MED22, RPL21P81, 1 more genes
    nsv6867166copy number variation1nstd229human GRCh38 chr9: 133,232,578-133,362,435 , GRCh37.p13 chr9|NW_003315925.1: 58,524-188,529 , GRCh37.p13 chr9: 136,107,965-136,229,311 SURF2, SURF6, 11 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
    nsv6453170copy number variation1nstd223human GRCh38 chr9: 133,331,053-133,344,786 , GRCh37.p13 chr9|NW_003315925.1: 157,147-170,880 , GRCh37.p13 chr9: 136,197,889-136,211,641 MED22, SURF6, 1 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
    nsv6304814copy number variation1nstd186human GRCh37 chr9: 136,197,889-136,211,641 , GRCh38.p12 chr9: 133,331,053-133,344,786 , GRCh38.p12 chr9|NW_009646201.1: 157,147-170,880 MED22, SURF6, 1 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
    nsv5488204copy number variation1nstd206human GRCh37.p13 chr9|NW_003315925.1: 157,147-170,880 , GRCh38 chr9: 133,331,053-133,344,786 , GRCh37.p13 chr9: 136,197,889-136,211,641 SURF6, RPL21P81, 1 more genes
    nsv5379540translocation1nstd200human GRCh38 chr9: 133,334,390-133,334,390 , GRCh38 chr9: 133,332,763-133,332,763 , GRCh37.p13 chr9|NW_003315925.1: 158,857-158,857 , GRCh37.p13 chr9|NW_003315925.1: 160,484-160,484 , GRCh37.p13 chr9: 136,199,599-136,199,599 , GRCh37.p13 chr9: 136,201,226-136,201,226 SURF6
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