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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148117copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,611,360-89,264,122 , GRCh38.p12 chr10: 79,851,604-87,504,365 ANXA11, FAM245A, 115 more genes
    nsv7146313insertion1nstd232human GRCh37.p13 chr10: 85,908,596-85,908,596 , GRCh38.p12 chr10: 84,148,840-84,148,840 GHITM
    nsv7141557insertion1nstd232human GRCh37.p13 chr10: 85,901,388-85,901,388 , GRCh38.p12 chr10: 84,141,632-84,141,632 GHITM
    nsv7139006insertion1nstd232human GRCh37.p13 chr10: 85,903,862-85,903,862 , GRCh38.p12 chr10: 84,144,106-84,144,106 GHITM
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6893720copy number variation1nstd229human GRCh38 chr10: 76,896,077-84,570,412 , GRCh37.p13 chr10: 78,655,835-86,330,168 RNU6-129P, LOC105378392, 111 more genes
    nsv6890901copy number variation1nstd229human GRCh38 chr10: 83,260,394-85,032,771 , GRCh37.p13 chr10: 85,020,150-86,792,527 RNU6-129P, TNPO1P1, 25 more genes
    nsv6885719copy number variation1nstd229human GRCh38 chr10: 84,134,059-84,139,345 , GRCh37.p13 chr10: 85,893,815-85,899,101 GHITM
    nsv6883647copy number variation1nstd229human GRCh38 chr10: 84,153,601-84,237,700 , GRCh37.p13 chr10: 85,913,357-85,997,456 GHITM, CDHR1, 4 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6634458copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320 IFIT5, IFIT1, 140 more genes
    nsv6585055inversion1nstd223human GRCh38 chr10: 79,754,380-87,461,415 , GRCh37.p13 chr10: 81,514,136-89,221,172 DYDC2, LOC105378394, 114 more genes
    nsv6448665copy number variation1nstd223human GRCh38 chr10: 84,137,080-84,144,555 , GRCh37.p13 chr10: 85,896,836-85,904,311 GHITM
    nsv6315478copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,630,468-88,980,961 , GRCh38.p12 chr10: 79,870,712-87,221,204 RNU1-19P, LOC107984187, 102 more genes
    nsv6247314mobile element insertion1nstd215human GRCh38 chr10: 84,140,771-84,140,771 , GRCh37.p13 chr10: 85,900,527-85,900,527 GHITM
    nsv5926561copy number variation1nstd209human GRCh38 chr10: 79,825,669-87,341,680 , GRCh37.p13 chr10: 81,585,425-89,101,437 , RPL12P29, 110 more genes
    nsv5039457inversion1nstd200human GRCh38 chr10: 84,138,634-84,960,031 , GRCh37.p13 chr10: 85,898,390-86,719,787 CCSER2, LRIT1, 14 more genes
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