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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4916933copy number variation1nstd200human GRCh38 chr2: 219,231,363-219,232,062 , GRCh37.p13 chr2: 220,096,085-220,096,784 ANKZF1
    nsv212472insertion1nstd6human NCBI35 chr2: 219,920,834-219,920,834 , GRCh37.p13 chr2: 220,095,329-220,095,329 , GRCh38.p12 chr2: 219,230,607-219,230,607 ANKZF1
    nsv6311484copy number variation1nstd102humanUncertain significance GRCh37 chr2: 220,097,339-220,100,931 , GRCh38.p12 chr2: 219,232,617-219,236,209 ANKZF1, GLB1L
    nsv7096609copy number variation1nstd102humanUncertain significance GRCh37 chr2: 220,101,115-220,102,134 , GRCh38.p12 chr2: 219,236,393-219,237,412 ANKZF1, GLB1L
    nsv6311637copy number variation1nstd102humanUncertain significance GRCh37 chr2: 220,101,116-220,102,135 , GRCh38.p12 chr2: 219,236,394-219,237,413 ANKZF1, GLB1L
    nsv6339958copy number variation1nstd223human GRCh38 chr2: 219,236,393-219,237,413 , GRCh37.p13 chr2: 220,101,115-220,102,135 ANKZF1, GLB1L
    nsv5439522copy number variation1nstd206human GRCh38 chr2: 219,236,393-219,237,413 , GRCh37.p13 chr2: 220,101,115-220,102,135 ANKZF1, GLB1L
    nsv4796019copy number variation1nstd200human GRCh37 chr2: 220,101,115-220,102,135 , GRCh38.p12 chr2: 219,236,393-219,237,413 ANKZF1, GLB1L
    nsv4777485mobile element deletion1nstd200human GRCh37 chr2: 220,101,482-220,101,790 , GRCh38.p12 chr2: 219,236,760-219,237,068 ANKZF1, GLB1L
    esv3828239copy number variation1estd219human GRCh37 chr2: 220,101,034-220,102,123 , GRCh38.p12 chr2: 219,236,312-219,237,401 ANKZF1, GLB1L
    esv3594357copy number variation1estd214human GRCh37 chr2: 220,101,034-220,102,123 , GRCh38.p12 chr2: 219,236,312-219,237,401 ANKZF1, GLB1L
    nsv820013copy number variation1nstd43human GRCh38.p12 chr2: 219,233,807-219,234,784 , NCBI36 chr2: 219,806,773-219,807,750 , GRCh37.p13 chr2: 220,098,529-220,099,506 ANKZF1, GLB1L
    nsv4569612mobile element insertion1nstd166human GRCh37.p13 chr2: 220,101,357-220,101,357 , GRCh38.p12 chr2: 219,236,635-219,236,635 ANKZF1, GLB1L
    esv1440894insertion1estd22human NCBI36 chr2: 219,809,748-219,809,748 , GRCh37.p13 chr2: 220,101,504-220,101,504 , GRCh38.p12 chr2: 219,236,782-219,236,782 ANKZF1, GLB1L
    nsv216514insertion1nstd6human NCBI35 chr2: 219,927,010-219,927,010 , GRCh37.p13 chr2: 220,101,505-220,101,505 , GRCh38.p12 chr2: 219,236,783-219,236,783 ANKZF1, GLB1L
    nsv5361329translocation1nstd200human GRCh38 chr2: 219,237,413-219,237,413 , GRCh38 chr2: 219,236,393-219,236,393 , GRCh37.p13 chr2: 220,101,115-220,101,115 , GRCh37.p13 chr2: 220,102,135-220,102,135 ANKZF1, GLB1L
    nsv1986166short tandem repeat3nstd128human GRCh37 chr2: 220,094,295-220,094,323 , GRCh38.p12 chr2: 219,229,573-219,229,601 ANKZF1, ATG9A
    nsv3127083copy number variation1nstd151human GRCh37 chr2: 220,097,798-220,112,341 , GRCh38.p12 chr2: 219,233,076-219,247,619 ANKZF1, GLB1L, 1 more genes
    nsv875870copy number variation8nstd71human NCBI36 chr2: 219,765,198-219,809,031 , GRCh37.p13 chr2: 220,056,954-220,100,787 , GRCh38.p12 chr2: 219,192,232-219,236,065 ANKZF1, ZFAND2B, 3 more genes
    nsv4089740copy number variation1nstd166human GRCh37.p13 chr2: 220,093,000-220,102,000 , GRCh38.p12 chr2: 219,228,278-219,237,278 ANKZF1, ATG9A, 1 more genes
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