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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4360270copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 127,883,695-129,583,785 , GRCh37.p13 chr9: 128,843,874-130,543,964 , GRCh38.p12 chr9: 126,081,595-127,781,685 RPL12, ZBTB43, 31 more genes
    nsv4360173copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 126,857,965-130,440,046 , GRCh37.p13 chr9: 127,818,144-131,400,225 , GRCh38.p12 chr9: 125,055,865-128,637,946 CDK9, LMX1B, 101 more genes
    nsv4360068copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 122,875,201-140,193,718 , GRCh37.p13 chr9: 123,835,380-141,073,897 , GRCh38.p12 chr9: 121,073,102-138,179,445 ABL1, ABO, 513 more genes
    nsv4359665copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 194,090-140,138,797 , GRCh37.p13 chr9: 204,090-141,018,976 , GRCh38.p12 chr9: 204,090-138,124,524 PLIN2, ALAD, 2240 more genes
    nsv4359064copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 122,914,494-140,089,497 , GRCh37.p13 chr9: 123,874,673-140,969,676 , GRCh38.p12 chr9: 121,112,395-138,075,224 ABL1, CACNA1B, 510 more genes
    nsv4358260copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 204,367-140,128,736 , GRCh37.p13 chr9: 214,367-141,008,915 , GRCh38.p12 chr9: 214,367-138,114,463 ABCA1, ACO1, 2240 more genes
    nsv4358131copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 124,897,698-128,495,943 , GRCh37.p13 chr9: 125,857,877-129,456,122 , GRCh38.p12 chr9: 123,095,598-126,693,843 PBX3, PPP6C, 68 more genes
    nsv4357831copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 194,193-140,138,805 , GRCh37.p13 chr9: 204,193-141,018,984 , GRCh38.p12 chr9: 204,193-138,124,532 ABO, AMBP, 2240 more genes
    nsv4357027copy number variation3nstd102humanPathogenic NCBI36 (hg18) chr9: 194,193-140,193,718 , GRCh37.p13 chr9: 204,193-141,073,897 , GRCh38.p12 chr9: 204,193-138,179,445 ABCA2, PLIN2, 2242 more genes
    nsv4356500copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 127,795,683-131,484,475 , GRCh37.p13 chr9: 128,755,862-132,444,654 , GRCh38.p12 chr9: 125,993,583-129,682,375 AK1, ENG, 117 more genes
    nsv4356079copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 67,910,461-140,173,346 , GRCh37.p13 chr9: 68,420,641-141,053,525 , GRCh38.p12 chr9: 40,915,719-138,159,073 ABCA1, AUH, 1604 more genes
    nsv4354305copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 124,594,758-140,138,805 , GRCh37.p13 chr9: 125,554,937-141,018,984 , GRCh38.p12 chr9: 122,792,658-138,124,532 ARF4P1, DNM1, 470 more genes
    nsv4352108copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 194,104-140,173,346 , GRCh37.p13 chr9: 204,104-141,053,525 , GRCh38.p12 chr9: 204,104-138,159,073 ABCA1, ABL1, 2242 more genes
    nsv4342237mobile element insertion1nstd166human GRCh37.p13 chr9: 6,831,380-134,099,063 , GRCh38.p12 chr9: 6,831,380-131,223,676 PLIN2, AK1, 1884 more genes
    nsv4340160mobile element insertion1nstd166human GRCh37.p13 chr9: 129,218,755-129,218,773 , GRCh38.p12 chr9: 126,456,476-126,456,494 MVB12B
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 ABL1, ABO, 926 more genes
    nsv4334245mobile element insertion1nstd166human GRCh37.p13 chr9: 129,100,807-129,100,821 , GRCh38.p12 chr9: 126,338,528-126,338,542 MVB12B
    nsv4326414mobile element insertion1nstd166human GRCh37.p13 chr9: 129,200,617-129,200,631 , GRCh38.p12 chr9: 126,438,338-126,438,352 MVB12B
    nsv4311401insertion1nstd166human GRCh37.p13 chr9: 129,131,196-129,131,213 , GRCh38.p12 chr9: 126,368,917-126,368,934 MVB12B
    nsv4310942insertion1nstd166human GRCh37.p13 chr9: 129,087,576-129,087,587 , GRCh38.p12 chr9: 126,325,297-126,325,308 MVB12B
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