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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907983copy number variation1nstd209human GRCh38 chr9: 124,480,949-124,481,267 , GRCh37.p13 chr9: 127,243,228-127,243,546 NR5A1
    nsv5633882insertion1nstd207human GRCh38 chr9: 124,488,840-124,488,840 , GRCh37.p13 chr9: 127,251,119-127,251,119 NR5A1
    nsv5318672copy number variation1nstd204human GRCh38.p13 chr9: 124,496,051-124,496,486 , GRCh37.p13 chr9: 127,258,330-127,258,765 NR5A1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4985704copy number variation1nstd200human GRCh38 chr9: 124,441,980-124,484,258 , GRCh37.p13 chr9: 127,204,259-127,246,537 NR5A1, ADGRD2, 1 more genes
    nsv4983603copy number variation1nstd200human GRCh38 chr9: 124,491,694-124,491,892 , GRCh37.p13 chr9: 127,253,973-127,254,171 NR5A1
    nsv4846364copy number variation1nstd200human GRCh37 chr9: 127,258,340-127,258,756 , GRCh38.p12 chr9: 124,496,061-124,496,477 NR5A1
    nsv4840463copy number variation1nstd200human GRCh37 chr9: 127,249,107-127,249,447 , GRCh38.p12 chr9: 124,486,828-124,487,168 NR5A1
    nsv4681126copy number variation1nstd102humanPathogenic GRCh37 chr9: 127,243,637-127,267,690 , GRCh38.p12 chr9: 124,481,358-124,505,411 NR5A1
    nsv4541158insertion1nstd166human GRCh37.p13 chr9: 127,258,431-127,258,431 , GRCh38.p12 chr9: 124,496,152-124,496,152 NR5A1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4178068copy number variation1nstd166human GRCh37.p13 chr9: 127,204,299-127,246,537 , GRCh38.p12 chr9: 124,442,020-124,484,258 LOC105376270, ADGRD2, 1 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3922263copy number variation1nstd102humanPathogenic NCBI36 chr9: 124,897,698-128,495,943 , GRCh38 chr9: 123,095,598-126,693,843 , GRCh37 chr9: 125,857,877-129,456,122 OLFML2A, LHX2-AS1, 64 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920829copy number variation1nstd102humanPathogenic GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497 LOC101928786, NRON, 495 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
    nsv3919948copy number variation1nstd102humanPathogenic GRCh37 chr9: 125,554,937-141,018,984 , GRCh38 chr9: 122,792,658-138,124,532 , NCBI36 chr9: 124,594,758-140,138,805 LOC107987143, ATP6V1G1P3, 456 more genes
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