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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887843copy number variation1nstd209human GRCh38 chr3: 86,962,827-86,962,882 , GRCh37.p13 chr3: 87,011,977-87,012,032 VGLL3
    nsv5681161mobile element insertion1nstd211human GRCh38 chr3: 86,969,773-86,969,773 , GRCh37.p13 chr3: 87,018,923-87,018,923 VGLL3
    nsv5437124copy number variation1nstd206human GRCh38 chr3: 86,947,719-86,954,679 , GRCh37.p13 chr3: 86,996,869-87,003,829 VGLL3
    nsv5436727copy number variation1nstd206human GRCh38 chr3: 86,908,927-86,939,977 , GRCh37.p13 chr3: 86,958,077-86,989,127 VGLL3, LOC105377196
    nsv5408160mobile element insertion1nstd206human GRCh38 chr3: 86,969,773-86,969,790 , GRCh37.p13 chr3: 87,018,923-87,018,940 VGLL3
    nsv5346189translocation1nstd200human GRCh38 chr3: 86,947,719-86,947,719 , GRCh38 chr3: 86,954,679-86,954,679 , GRCh37.p13 chr3: 86,996,869-86,996,869 , GRCh37.p13 chr3: 87,003,829-87,003,829 VGLL3
    nsv5339776translocation1nstd200human GRCh37 chr3: 87,035,287-87,035,287 , GRCh37 chr3: 87,035,362-87,035,362 , GRCh38.p12 chr3: 86,986,137-86,986,137 , GRCh38.p12 chr3: 86,986,212-86,986,212 VGLL3
    nsv5098559mobile element insertion1nstd203human GRCh38 chr3: 86,988,684-86,988,684 , GRCh37.p13 chr3: 87,037,834-87,037,834 VGLL3
    nsv5096744mobile element insertion1nstd203human GRCh38 chr3: 86,988,640-86,988,685 , GRCh37.p13 chr3: 87,037,790-87,037,835 VGLL3
    nsv5093157mobile element insertion1nstd203human GRCh38 chr3: 86,988,685-86,988,685 , GRCh37.p13 chr3: 87,037,835-87,037,835 VGLL3
    nsv5089464mobile element insertion1nstd203human GRCh38 chr3: 86,988,680-86,988,680 , GRCh37.p13 chr3: 87,037,830-87,037,830 VGLL3
    nsv4929038copy number variation1nstd200human GRCh38 chr3: 86,784,014-87,815,346 , GRCh37.p13 chr3: 86,833,164-87,864,496 LOC105377196, VGLL3, 12 more genes
    nsv4927686copy number variation1nstd200human GRCh38 chr3: 86,986,137-86,986,212 , GRCh37.p13 chr3: 87,035,287-87,035,362 VGLL3
    nsv4927685copy number variation1nstd200human GRCh38 chr3: 86,952,093-86,956,400 , GRCh37.p13 chr3: 87,001,243-87,005,550 VGLL3
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4797348copy number variation1nstd200human GRCh37 chr3: 86,996,869-87,003,829 , GRCh38.p12 chr3: 86,947,719-86,954,679 VGLL3
    nsv4797347copy number variation1nstd200human GRCh37 chr3: 86,988,961-86,989,372 , GRCh38.p12 chr3: 86,939,811-86,940,222 VGLL3
    nsv4674591copy number variation1nstd102humanUncertain significance GRCh37 chr3: 86,841,600-87,862,816 , GRCh38.p12 chr3: 86,792,450-87,813,666 PSMC1P6, LOC105377196, 12 more genes
    nsv4586886copy number variation1nstd183human GRCh37 chr3: 86,990,346-86,994,860 , GRCh38.p12 chr3: 86,941,196-86,945,710 VGLL3
    nsv4568251inversion1nstd166human GRCh37.p13 chr3: 81,845,861-90,137,796 , GRCh38.p12 chr3: 81,796,710-90,088,646 POU1F1, CHMP2B, 54 more genes
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