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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075189inversion1nstd229human GRCh38 chr13: 38,938,572-45,892,931 , GRCh37.p13 chr13: 39,512,709-46,467,066 TPT1-AS1, AKAP11, 136 more genes
    nsv7070608inversion1nstd229human GRCh38 chr13: 37,808,702-41,386,678 , GRCh37.p13 chr13: 38,382,839-41,960,814 FREM2-AS1, SUGT1P3, 63 more genes
    nsv7068559inversion1nstd229human GRCh38 chr13: 38,569,400-39,735,090 , GRCh37.p13 chr13: 39,143,537-40,309,227 LOC105370170, RNU6-56P, 19 more genes
    nsv7060789inversion1nstd229human GRCh38 chr13: 38,967,784-43,058,064 , GRCh37.p13 chr13: 39,541,921-43,632,200 RGCC, RAC1P3, 79 more genes
    nsv6957243copy number variation1nstd229human GRCh38 chr13: 38,960,898-39,169,443 , GRCh37.p13 chr13: 39,535,035-39,743,580 NXT1P1, PROSER1, 3 more genes
    nsv6953785copy number variation1nstd229human GRCh38 chr13: 39,010,129-39,010,191 , GRCh37.p13 chr13: 39,584,266-39,584,328 PROSER1
    nsv6944386copy number variation1nstd229human GRCh38 chr13: 39,030,893-39,030,987 , GRCh37.p13 chr13: 39,605,030-39,605,124 PROSER1
    nsv6941951copy number variation1nstd229human GRCh38 chr13: 38,198,441-39,401,517 , GRCh37.p13 chr13: 38,772,578-39,975,654 NXT1P1, LOC105370168, 17 more genes
    nsv6637985copy number variation1nstd102humanUncertain significance GRCh37 chr13: 36,148,057-41,670,428 , GRCh38.p12 chr13: 35,573,920-41,096,292 RPS12P24, SPART, 86 more genes
    nsv6637238copy number variation1nstd102humanPathogenic GRCh37 chr13: 35,501,428-40,901,176 , GRCh38.p12 chr13: 34,927,291-40,327,039 CCDC169-SOHLH2, RNA5SP26, 74 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6493329copy number variation1nstd223human GRCh38 chr13: 38,960,898-39,169,443 , GRCh37.p13 chr13: 39,535,035-39,743,580 NHLRC3, STOML3, 3 more genes
    nsv6492126copy number variation1nstd223human GRCh38 chr13: 39,034,801-39,042,000 , GRCh37.p13 chr13: 39,608,938-39,616,137 PROSER1, NHLRC3
    nsv6487978copy number variation1nstd223human GRCh38 chr13: 39,030,485-39,030,857 , GRCh37.p13 chr13: 39,604,622-39,604,994 PROSER1
    nsv6485082copy number variation1nstd223human GRCh38 chr13: 39,033,301-39,038,000 , GRCh37.p13 chr13: 39,607,438-39,612,137 PROSER1, NHLRC3
    nsv6481829copy number variation1nstd223human GRCh38 chr13: 39,012,686-39,080,254 , GRCh37.p13 chr13: 39,586,823-39,654,391 PROSER1, NHLRC3
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6313982copy number variation1nstd102humanUncertain significance GRCh37 chr13: 39,428,367-43,608,103 , GRCh38.p12 chr13: 38,854,230-43,033,967 DGKH, ELF1, 82 more genes
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