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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4356213copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr19: 42,502,119-47,934,680 , GRCh37.p13 chr19: 37,810,279-43,242,840 , GRCh38.p12 chr19: 37,319,377-42,738,688 ACTN4, CEACAM1, 237 more genes
    nsv4355432copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr19: 11,199,618-49,821,491 , GRCh37.p13 chr19: 11,338,618-45,129,651 , GRCh38.p12 chr19: 11,227,942-44,626,354 CEACAM1, CALR, 1129 more genes
    nsv4345458sequence alteration1nstd166human GRCh37.p13 chr19: 39,251,089-39,325,973 , GRCh38.p12 chr19|NW_014040929.1: 170,058-245,005 , GRCh38.p12 chr19: 38,760,449-38,835,333 HNRNPL, ECH1, 4 more genes
    nsv4320730insertion1nstd166human GRCh37.p13 chr19: 3,945,039-46,484,212 , GRCh38.p12 chr19: 3,945,041-45,980,954 ACP5, AKT2, 1499 more genes
    nsv4320724insertion1nstd166human GRCh37.p13 chr19: 14,891,392-47,384,391 , GRCh38.p12 chr19: 14,780,580-46,881,134 ACTN4, APOC1, 1059 more genes
    nsv4268467copy number variation1nstd166human GRCh37.p13 chr19: 39,249,462-39,309,420 , GRCh38.p12 chr19|NW_014040929.1: 168,431-228,452 , GRCh38.p12 chr19: 38,758,822-38,818,780 ECH1, LGALS4, 3 more genes
    nsv4256336copy number variation1nstd166human GRCh37.p13 chr19: 39,261,000-39,280,000 , GRCh38.p12 chr19: 38,770,360-38,789,360 LGALS7B, LGALS7
    nsv4017720mobile element insertion1nstd166human GRCh37.p13 chr19: 36,728,722-39,414,168 , GRCh38.p12 chr19: 36,237,820-38,923,528 ACTN4, HNRNPL, 90 more genes
    nsv4013004mobile element insertion1nstd166human GRCh37.p13 chr19: 14,824,951-46,797,145 , GRCh38.p12 chr19: 14,714,139-46,293,888 APLP1, APOC1P1, 1035 more genes
    nsv3909325copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr19: 39,234,888-39,294,200 , GRCh38.p12 chr19: 38,744,248-38,803,560 , GRCh38.p12 chr19|NW_014040929.1: 153,852-213,225 , NCBI36 (hg18) chr19: 43,926,728-43,986,040 LGALS4, LGALS7, 3 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 , NCBI36 (hg18) chr19: 19,029-63,802,102 BNIP3P32, TMEM205, 2489 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 , NCBI36 (hg18) chr19: 211,912-63,788,972 TYMSP2, GP6, 2472 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 (hg19) chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 , NCBI36 (hg18) chr19: 211,912-63,648,700 LOC100128398, RPL12P42, 2453 more genes
    nsv3895066copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003 , NCBI36 (hg18) chr19: 42,274,090-46,322,748 LGALS7, PAF1, 165 more genes
    nsv3891951copy number variation1nstd102humanconflicting data from submitters GRCh37 (hg19) chr19: 39,262,641-39,281,318 , NCBI36 (hg18) chr19: 43,954,481-43,973,158 , GRCh38.p12 chr19: 38,772,001-38,790,678 LGALS7, LGALS7B
    nsv3371532inversion12nstd162human GRCh38 (hg38) chr19: 38,769,343-38,782,967 , GRCh37.p13 chr19: 39,259,983-39,273,607 LGALS7
    nsv3234976insertion1nstd152human GRCh38 (hg38) chr19: 38,758,851-38,799,961 , GRCh37.p13 chr19: 39,249,491-39,290,601 LGALS7, LGALS4, 2 more genes
    nsv3233670insertion1nstd152human GRCh38 (hg38) chr19: 38,760,981-38,799,961 , GRCh37.p13 chr19: 39,251,621-39,290,601 LGALS7, LGALS4, 2 more genes
    nsv3225090copy number variation1nstd152human GRCh38 (hg38) chr19: 38,760,981-38,799,961 , GRCh37.p13 chr19: 39,251,621-39,290,601 RNU6-140P, LGALS7B, 2 more genes
    nsv3215080copy number variation3nstd152human GRCh38 (hg38) chr19: 38,758,851-38,780,634 , GRCh37.p13 chr19: 39,249,491-39,271,274 LGALS7
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