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Items: 1 to 20 of 225

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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
    nsv7093414copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409 LHX3, FUT7, 121 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
    nsv7072643inversion1nstd229human GRCh38 chr9: 135,458,665-135,526,031 , GRCh37.p13 chr9: 138,350,511-138,417,877 MRPS2, PIERCE1, 4 more genes
    nsv7067587inversion1nstd229human GRCh38 chr9: 135,458,655-135,516,088 , GRCh37.p13 chr9: 138,350,501-138,407,934 PPP1R26, LOC101928525, 3 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
    nsv6897387copy number variation1nstd229human GRCh38 chr9: 135,332,402-135,692,664 , GRCh37.p13 chr9: 138,224,248-138,584,510 LOC105376318, GLT6D1, 18 more genes
    nsv6889819copy number variation1nstd229human GRCh38 chr9: 135,123,339-135,604,638 , GRCh37.p13 chr9: 138,015,185-138,496,484 LINC01502, LOC107987040, 15 more genes
    nsv6887693copy number variation1nstd229human GRCh38 chr9: 135,237,361-135,592,284 , GRCh37.p13 chr9: 138,129,207-138,484,130 PPP1R26, LINC02907, 13 more genes
    nsv6883347copy number variation1nstd229human GRCh38 chr9: 135,500,309-135,623,544 , GRCh37.p13 chr9: 138,392,155-138,515,390 OBP2A, MRPS2, 10 more genes
    nsv6879912copy number variation1nstd229human GRCh38 chr9: 135,500,295-135,504,371 , GRCh37.p13 chr9: 138,392,141-138,396,217 MRPS2, LOC101928525, 1 more genes
    nsv6633223copy number variation1nstd224human GRCh37 chr9: 138,236,212-138,490,710 , GRCh38.p12 chr9: 135,344,366-135,598,864 LCN1, PPP1R26, 12 more genes
    nsv6568727inversion1nstd223human GRCh38 chr9: 135,458,657-135,516,088 , GRCh37.p13 chr9: 138,350,503-138,407,934 PPP1R26, MRPS2, 3 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
    nsv6312761copy number variation2nstd102humanUncertain significance GRCh37 chr9: 137,534,034-139,440,238 , GRCh38.p12 chr9: 134,642,188-136,545,786 COL5A1-AS1, C9orf163, 61 more genes
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