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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896467copy number variation1nstd209human GRCh38 chr4: 86,411,170-87,486,334 , GRCh37.p13 chr4: 87,332,323-88,407,486 , MIR4452, 21 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5310624copy number variation1nstd204human GRCh38.p13 chr4: 86,789,365-87,210,443 , GRCh37.p13 chr4: 87,710,518-88,131,595 AFF1, RPL6P13, 10 more genes
    nsv5239177copy number variation1nstd204human GRCh37.p13 chr4: 87,711,154-87,943,452 , GRCh38.p13 chr4: 86,790,001-87,022,300 AFF1, PTPN13, 6 more genes
    nsv5235088copy number variation1nstd204human GRCh38.p13 chr4: 86,873,931-86,876,030 , GRCh37.p13 chr4: 87,795,084-87,797,183 C4orf36
    nsv5085261mobile element insertion1nstd203human GRCh38 chr4: 86,888,434-86,888,450 , GRCh37.p13 chr4: 87,809,587-87,809,603 C4orf36
    nsv5040446inversion1nstd200human GRCh38 chr4: 76,223,829-89,968,114 , GRCh37.p13 chr4: 77,144,982-90,889,265 , KPNA2P1, 209 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4929340copy number variation1nstd200human GRCh38 chr4: 86,845,822-86,949,508 , GRCh37.p13 chr4: 87,766,975-87,870,660 AFF1, C4orf36, 5 more genes
    nsv4923419copy number variation1nstd200human GRCh38 chr4: 86,887,981-86,906,766 , GRCh37.p13 chr4: 87,809,134-87,827,919 C4orf36
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    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
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4729598copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632 PTPN11P5, LOC643014, 244 more genes
    nsv4729331copy number variation1nstd102humanUncertain significance GRCh37 chr4: 87,704,091-88,223,403 , GRCh38.p12 chr4: 86,782,938-87,302,251 GAPDHP60, KLHL8, 12 more genes
    nsv4716198copy number variation1nstd195human GRCh37 chr4: 87,808,251-87,902,001 , GRCh38.p12 chr4: 86,887,098-86,980,849 AFF1, C4orf36, 3 more genes
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