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Items: 1 to 20 of 175

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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
    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
    nsv6893066copy number variation1nstd229human GRCh38 chr10: 84,291,949-84,294,444 , GRCh37.p13 chr10: 86,051,705-86,054,200 LINC00858
    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
    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
    nsv6454259copy number variation1nstd223human GRCh38 chr10: 84,287,901-84,312,600 , GRCh37.p13 chr10: 86,047,657-86,072,356 LINC00858
    nsv6448215copy number variation1nstd223human GRCh38 chr10: 84,291,949-84,294,443 , GRCh37.p13 chr10: 86,051,705-86,054,199 LINC00858
    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
    nsv5926561copy number variation1nstd209human GRCh38 chr10: 79,825,669-87,341,680 , GRCh37.p13 chr10: 81,585,425-89,101,437 , RPL12P29, 110 more genes
    nsv5721394mobile element insertion2nstd211human GRCh38 chr10: 84,278,170-84,278,170 , GRCh37.p13 chr10: 86,037,926-86,037,926 LINC00858
    nsv5315834copy number variation1nstd204human GRCh38.p13 chr10: 84,193,962-84,300,656 , GRCh37.p13 chr10: 85,953,718-86,060,412 RGR, LRIT2, 3 more genes
    nsv5243734copy number variation1nstd204human GRCh38.p13 chr10: 84,211,401-84,300,600 , GRCh37.p13 chr10: 85,971,157-86,060,356 LRIT2, CDHR1, 3 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
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
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