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Items: 1 to 20 of 289

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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
    nsv5961432insertion1nstd209human GRCh38 chr4: 16,194,861-16,194,861 , GRCh37.p13 chr4: 16,196,484-16,196,484 TAPT1
    nsv5620939insertion1nstd207human GRCh38 chr4: 16,194,855-16,194,855 , GRCh37.p13 chr4: 16,196,478-16,196,478 TAPT1
    nsv5619512insertion1nstd207human GRCh38 chr4: 16,194,859-16,194,859 , GRCh37.p13 chr4: 16,196,482-16,196,482 TAPT1
    nsv5381429copy number variation1nstd102humanUncertain significance GRCh37 chr4: 15,964,081-16,172,352 , GRCh38.p12 chr4: 15,962,458-16,170,729 LOC105374502, PROM1, 3 more genes
    nsv5352591translocation1nstd200human GRCh38 chr4: 16,168,309-16,168,309 , GRCh38 chr4: 16,167,218-16,167,218 , GRCh37.p13 chr4: 16,169,932-16,169,932 , GRCh37.p13 chr4: 16,168,841-16,168,841 TAPT1
    nsv5199773mobile element insertion1nstd203human GRCh38 chr4: 16,171,284-16,171,297 , GRCh37.p13 chr4: 16,172,907-16,172,920 TAPT1
    nsv5097985mobile element insertion1nstd203human GRCh38 chr4: 16,203,319-16,203,331 , GRCh37.p13 chr4: 16,204,942-16,204,954 TAPT1
    nsv5091879mobile element insertion1nstd203human GRCh38 chr4: 16,182,064-16,182,077 , GRCh37.p13 chr4: 16,183,687-16,183,700 TAPT1
    nsv5089617mobile element insertion1nstd203human GRCh38 chr4: 16,218,561-16,218,574 , GRCh37.p13 chr4: 16,220,184-16,220,197 TAPT1
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4925312copy number variation1nstd200human GRCh38 chr4: 13,546,371-16,224,534 , GRCh37.p13 chr4: 13,547,995-16,226,157 , LOC107986261, 38 more genes
    nsv4921700copy number variation1nstd200human GRCh38 chr4: 16,215,845-16,215,996 , GRCh37.p13 chr4: 16,217,468-16,217,619 TAPT1
    nsv4921699copy number variation1nstd200human GRCh38 chr4: 16,157,145-16,159,550 , GRCh37.p13 chr4: 16,158,768-16,161,173 TAPT1
    nsv4809057copy number variation1nstd200human GRCh37 chr4: 13,547,995-16,226,157 , GRCh38.p12 chr4: 13,546,371-16,224,534 , RPL10AP7, 38 more genes
    nsv4799569copy number variation1nstd200human GRCh37 chr4: 16,168,840-16,169,933 , GRCh38.p12 chr4: 16,167,217-16,168,310 TAPT1
    nsv4778003mobile element deletion1nstd200human GRCh37 chr4: 16,190,260-16,190,560 , GRCh38.p12 chr4: 16,188,637-16,188,937 TAPT1
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
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