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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098070copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999 STPG3-AS1, CACNA1B-AS1, 132 more genes
    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
    nsv7073511inversion1nstd229human GRCh38 chr9: 135,525,863-135,544,347 , GRCh37.p13 chr9: 138,417,709-138,436,193 OBP2A, LCN1
    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
    nsv6891772copy number variation1nstd229human GRCh38 chr9: 135,545,723-135,548,136 , GRCh37.p13 chr9: 138,437,569-138,439,982 OBP2A
    nsv6891017copy number variation1nstd229human GRCh38 chr9: 135,544,906-135,549,840 , GRCh37.p13 chr9: 138,436,752-138,441,686 OBP2A
    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
    nsv6889772copy number variation1nstd229human GRCh38 chr9: 135,546,346-135,546,373 , GRCh37.p13 chr9: 138,438,192-138,438,219 OBP2A
    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
    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
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6445483copy number variation1nstd223human GRCh38 chr9: 135,545,731-135,548,136 , GRCh37.p13 chr9: 138,437,577-138,439,982 OBP2A
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
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