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Items: 1 to 20 of 766

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5893138copy number variation1nstd209human GRCh38 chr4: 73,241-74,219 , GRCh37.p13 chr4|NW_004775427.1: 63,241-64,219 , GRCh37.p13 chr4: 73,133-74,112 ZNF595
    nsv5840400copy number variation1nstd209human GRCh38 chr4: 79,896-81,895 , GRCh37.p13 chr4|NW_004775427.1: 69,896-71,895 , GRCh37.p13 chr4: 79,789-81,788 ZNF595
    nsv5840031copy number variation1nstd209human GRCh38 chr4: 68,613-73,412 , GRCh37.p13 chr4|NW_004775427.1: 58,613-63,412 , GRCh37.p13 chr4: 68,718-73,304 ZNF595
    nsv5839839copy number variation1nstd209human GRCh38 chr4: 86,396-89,632 , GRCh37.p13 chr4|NW_004775427.1: 76,396-79,632 , GRCh37.p13 chr4: 86,286-89,520 ZNF595
    nsv5839790copy number variation1nstd209human GRCh38 chr4: 74,113-83,495 , GRCh37.p13 chr4|NW_004775427.1: 64,113-73,495 , GRCh37.p13 chr4: 74,006-83,387 ZNF595
    nsv5839486copy number variation1nstd209human GRCh38 chr4: 76,646-80,895 , GRCh37.p13 chr4: 76,539-80,788 , GRCh37.p13 chr4|NW_004775427.1: 66,646-70,895 ZNF595
    nsv5687435mobile element insertion2nstd211human GRCh38 chr4: 88,054-88,054 , GRCh37.p13 chr4|NW_004775427.1: 78,054-78,054 , GRCh37.p13 chr4: 87,942-87,942 ZNF595
    nsv5673565copy number variation1nstd102humanUncertain significance GRCh38 chr4: 1-705,161 , GRCh37.p13 chr4|NW_004775427.1: 1-503,215 , GRCh37.p13 chr4: 10,001-507,004 ABCA11P, LOC105374377, 23 more genes
    nsv5623828insertion1nstd207human GRCh38 chr4: 52,767-52,767 , GRCh37.p13 chr4|NW_004775427.1: 42,767-42,767 ZNF595
    nsv5622236insertion1nstd207human GRCh38 chr4: 68,825-68,825 , GRCh37.p13 chr4|NW_004775427.1: 58,825-58,825 ZNF595
    nsv5615272insertion1nstd207human GRCh38 chr4: 73,241-73,241 , GRCh37.p13 chr4|NW_004775427.1: 63,241-63,241 , GRCh37.p13 chr4: 73,133-73,133 ZNF595
    nsv5580546copy number variation1nstd207human GRCh38 chr4: 68,825-69,362 , GRCh37.p13 chr4: 68,718-69,254 , GRCh37.p13 chr4|NW_004775427.1: 58,825-59,362 ZNF595
    nsv5568184copy number variation1nstd207human GRCh38 chr4: 64,633-67,994 , GRCh37.p13 chr4|NW_004775427.1: 54,633-57,994 ZNF595
    nsv5450108copy number variation1nstd206human GRCh37.p13 chr4|NW_004775427.1: 27,861-125,262 , GRCh38 chr4: 37,861-135,262 , GRCh37.p13 chr4: 68,718-129,007 LOC105374377, ZNF595, 2 more genes
    nsv5440338copy number variation1nstd206human GRCh37.p13 chr4|NW_004775427.1: 17,400-221,000 , GRCh38 chr4: 27,400-231,000 , GRCh37.p13 chr4: 68,718-224,789 ZNF595, ZNF718, 4 more genes
    nsv5436618copy number variation1nstd206human GRCh38 chr4: 73,241-74,222 , GRCh37.p13 chr4|NW_004775427.1: 63,241-64,222 , GRCh37.p13 chr4: 73,133-74,115 ZNF595
    nsv5408375mobile element insertion1nstd206human GRCh38 chr4: 88,054-88,105 , GRCh37.p13 chr4|NW_004775427.1: 78,054-78,105 , GRCh37.p13 chr4: 87,942-87,993 ZNF595
    nsv5385752copy number variation1nstd186human GRCh37 chr4: 64,513-67,887 , GRCh38.p12 chr4: 64,621-67,995 ZNF595
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