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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
    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
    nsv7078061inversion1nstd229human GRCh38 chr9: 137,430,479-137,430,580 , GRCh37.p13 chr9: 140,324,931-140,325,032 NOXA1
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 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
    nsv6897245copy number variation1nstd229human GRCh38 chr9: 137,409,888-137,432,487 , GRCh37.p13 chr9: 140,304,340-140,326,939 EXD3, NOXA1, 1 more genes
    nsv6893989copy number variation1nstd229human GRCh38 chr9: 137,426,654-137,429,112 , GRCh37.p13 chr9: 140,321,106-140,323,564 NOXA1
    nsv6889470copy number variation1nstd229human GRCh38 chr9: 137,420,993-137,426,156 , GRCh37.p13 chr9: 140,315,445-140,320,608 NOXA1, EXD3
    nsv6887616copy number variation1nstd229human GRCh38 chr9: 137,409,042-137,437,646 , GRCh37.p13 chr9: 140,303,494-140,332,098 EXD3, ENTPD8, 1 more genes
    nsv6884175copy number variation1nstd229human GRCh38 chr9: 137,414,178-137,425,648 , GRCh37.p13 chr9: 140,308,630-140,320,100 NOXA1, EXD3
    nsv6633687copy number variation1nstd224human GRCh37 chr9: 140,320,715-140,449,965 , GRCh38.p12 chr9: 137,426,263-137,555,513 NOXA1, NSMF, 5 more genes
    nsv6452448copy number variation1nstd223human GRCh38 chr9: 137,413,376-137,443,504 , GRCh37.p13 chr9: 140,307,828-140,337,956 EXD3, NOXA1, 1 more genes
    nsv6451560copy number variation1nstd223human GRCh38 chr9: 137,410,037-137,454,256 , GRCh37.p13 chr9: 140,304,489-140,348,708 NSMF, MIR7114, 3 more genes
    nsv6448743copy number variation1nstd223human GRCh38 chr9: 137,420,993-137,426,156 , GRCh37.p13 chr9: 140,315,445-140,320,608 NOXA1, EXD3
    nsv6447760copy number variation1nstd223human GRCh38 chr9: 137,424,583-137,425,449 , GRCh37.p13 chr9: 140,319,035-140,319,901 NOXA1
    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
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