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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147055insertion1nstd232human GRCh37.p13 chr1: 70,698,059-70,698,059 , GRCh38.p12 chr1: 70,232,376-70,232,376 SRSF11
    nsv7099298copy number variation1nstd231human GRCh38.p12 chr1: 68,115,402-81,183,740 , GRCh37 chr1: 68,581,085-81,649,425 ACADM, COX6A1P1, 145 more genes
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7055498inversion1nstd229human GRCh38 chr1: 66,514,766-73,182,042 , GRCh37.p13 chr1: 66,980,449-73,647,725 LINC02796, LOC105378789, 80 more genes
    nsv7053920inversion1nstd229human GRCh38 chr1: 67,470,120-71,187,985 , GRCh37.p13 chr1: 67,935,803-71,653,668 LOC107984967, LOC105378787, 53 more genes
    nsv7051964inversion1nstd229human GRCh38 chr1: 67,266,655-71,123,545 , GRCh37.p13 chr1: 67,732,338-71,589,228 CHORDC1P5, IL12RB2, 58 more genes
    nsv6654010copy number variation1nstd229human GRCh38 chr1: 70,191,801-70,260,700 , GRCh37.p13 chr1: 70,657,484-70,726,383 LRRC40, SRSF11, 1 more genes
    nsv6653798copy number variation1nstd229human GRCh38 chr1: 70,228,401-70,235,600 , GRCh37.p13 chr1: 70,694,084-70,701,283 SRSF11
    nsv6653797copy number variation1nstd229human GRCh38 chr1: 70,222,207-70,336,045 , GRCh37.p13 chr1: 70,687,890-70,801,728 SRSF11, ANKRD13C
    nsv6653796copy number variation1nstd229human GRCh38 chr1: 70,194,101-70,266,000 , GRCh37.p13 chr1: 70,659,784-70,731,683 LRRC40, ANKRD13C, 1 more genes
    nsv6653260copy number variation1nstd229human GRCh38 chr1: 70,241,004-70,244,571 , GRCh37.p13 chr1: 70,706,687-70,710,254 SRSF11
    nsv6636817copy number variation1nstd102humanUncertain significance GRCh37 chr1: 69,989,275-72,180,606 , GRCh38.p12 chr1: 69,523,592-71,714,923 LOC102724572, ANKRD13C, 24 more genes
    nsv6626277copy number variation1nstd224human GRCh37 chr1: 70,697,933-70,781,186 , GRCh38.p12 chr1: 70,232,250-70,315,503 ANKRD13C, SRSF11
    nsv6550502inversion1nstd223human GRCh38 chr1: 70,212,376-70,212,967 , GRCh37.p13 chr1: 70,678,059-70,678,650 SRSF11
    nsv6542115inversion1nstd223human GRCh38 chr1: 61,925,268-71,371,290 , GRCh37.p13 chr1: 62,390,940-71,836,973 PATJ, GNG12-AS1, 142 more genes
    nsv6334582copy number variation1nstd223human GRCh38 chr1: 70,251,899-70,252,379 , GRCh37.p13 chr1: 70,717,582-70,718,062 SRSF11
    nsv6330538copy number variation1nstd223human GRCh38 chr1: 70,249,903-70,250,304 , GRCh37.p13 chr1: 70,715,586-70,715,987 SRSF11
    nsv6327085copy number variation1nstd223human GRCh38 chr1: 70,222,207-70,336,039 , GRCh37.p13 chr1: 70,687,890-70,801,722 SRSF11, ANKRD13C
    nsv6326981copy number variation1nstd223human GRCh38 chr1: 70,251,301-70,252,800 , GRCh37.p13 chr1: 70,716,984-70,718,483 SRSF11
    nsv6315306copy number variation1nstd102humanUncertain significance GRCh38 chr1: 66,885,559-77,949,895 , GRCh37.p13 chr1: 67,351,242-78,415,580 DNAJB6P4, LRRC7, 137 more genes
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