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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 TXNDC17, RPS4XP17, 289 more genes
    nsv3915884copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093 TXNDC17, LOC105371592, 222 more genes
    nsv3923152copy number variation1nstd102humanPathogenic NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343 TXNDC17, PSMB6, 133 more genes
    nsv3910343copy number variation1nstd102humanPathogenic GRCh37 chr17: 5,636,297-7,942,140 , NCBI36 chr17: 5,577,021-7,882,865 , GRCh38 chr17: 5,732,977-8,038,822 TXNDC17, RPL23AP73, 106 more genes
    nsv3883443copy number variation2nstd102humanPathogenic GRCh37 chr17: 6,328,760-6,616,672 , GRCh38.p12 chr17: 6,425,440-6,713,353 TXNDC17, PITPNM3, 11 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 TXNDC17, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 TXNDC17, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 TXNDC17, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 TXNDC17, SMURF2, 2366 more genes
    nsv3897625copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420 TXNDC17, GP1BA, 439 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 TXNDC17, KIF1C-AS1, 433 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 TXNDC17, PSMB6, 409 more genes
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 TXNDC17, RFLNB, 401 more genes
    nsv3904771copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115 TXNDC17, SLC2A4, 401 more genes
    nsv3917777copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-7,394,448 , GRCh38 chr17: 198,748-7,491,129 , NCBI36 chr17: 48,539-7,335,172 TXNDC17, PAFAH1B1, 267 more genes
    nsv3911050copy number variation1nstd102humanPathogenic GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391 TXNDC17, C17orf49, 209 more genes
    nsv3904710copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,113,102-6,742,486 , GRCh38.p12 chr17: 1,209,808-6,839,167 TXNDC17, OR1A2, 197 more genes
    nsv3911018copy number variation1nstd102humanLikely pathogenic NCBI36 chr17: 6,205,437-7,594,906 , GRCh37 chr17: 6,264,713-7,654,181 , GRCh38 chr17: 6,361,393-7,750,863 TXNDC17, ACADVL, 87 more genes
    nsv6291479copy number variation1nstd102humanUncertain significance GRCh37 chr17: 6,248,108-6,637,236 , GRCh38.p12 chr17: 6,344,788-6,733,917 TXNDC17, PITPNM3, 12 more genes
    nsv7095341copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,289,526-6,616,652 , GRCh38.p12 chr17: 5,386,206-6,713,333 TXNDC17, RNA5SP435, 31 more genes
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