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Items: 1 to 20 of 266

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098071copy number variation2nstd102humanPathogenic GRCh37 chr9: 139,089,171-141,016,451 , GRCh38.p12 chr9: 136,197,325-138,121,999 NPDC1, LOC101928786, 108 more genes
    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
    nsv7097938copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 140,040,158-141,016,451 , GRCh38.p12 chr9: 137,145,706-138,121,999 NELFB, LOC651337, 39 more genes
    nsv7097705copy number variation1nstd102humanPathogenic GRCh37 chr9: 140,513,481-140,657,292 , GRCh38.p12 chr9: 137,619,029-137,762,840 EHMT1, ARRDC1-AS1, 1 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
    nsv7068117inversion1nstd229human GRCh38 chr9: 137,246,535-138,000,327 , GRCh37.p13 chr9: 140,140,987-140,894,779 NELFB, MIR7114, 23 more genes
    nsv6633600copy number variation1nstd224human GRCh37 chr9: 140,498,095-140,648,752 , GRCh38.p12 chr9: 137,603,643-137,754,300 EHMT1, ARRDC1, 2 more genes
    nsv6451331copy number variation1nstd223human GRCh38 chr9: 137,598,046-137,669,216 , GRCh37.p13 chr9: 140,492,498-140,563,668 ARRDC1, SETP5, 2 more genes
    nsv6314096copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,230,197-140,893,129 , GRCh38.p12 chr9: 137,335,745-137,998,677 ARRDC1-AS1, NOXA1, 17 more genes
    nsv6313935copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,740,078-141,020,389 , GRCh38.p12 chr9: 135,848,232-138,125,937 ENTR1, LINC02692, 115 more genes
    nsv6313928copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,493,726-140,766,254 , GRCh38.p12 chr9: 137,599,274-137,871,802 MIR602, ARRDC1-AS1, 6 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
    nsv6291248copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,357,902-140,602,791 , GRCh38.p12 chr9: 137,463,450-137,708,339 ZMYND19, PNPLA7, 6 more genes
    nsv6291064copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,475,437-141,020,389 , GRCh38.p12 chr9: 137,580,985-138,125,937 ZMYND19, ARRDC1, 10 more genes
    nsv6137446copy number variation1nstd213human GRCh37 chr9: 138,580,000-141,150,001 , GRCh38.p12 chr9: 135,688,154-138,259,551 ABCA2, C8G, 123 more genes
    nsv6137066copy number variation1nstd213human GRCh37 chr9: 140,280,000-140,600,001 , GRCh38.p12 chr9: 137,385,548-137,705,549 NOXA1, EXD3, 11 more genes
    nsv5673888copy number variation1nstd102humanPathogenic GRCh37 chr9: 140,513,481-141,016,451 , GRCh38.p12 chr9: 137,619,029-138,121,999 EHMT1, LOC100133077, 8 more genes
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5381736copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,764,148-141,066,491 , GRCh38.p12 chr9: 136,869,696-138,172,039 PTGDS, LCN12, 63 more genes
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