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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098039copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,053,597-87,755,855 , GRCh38.p12 chr8: 85,141,362-86,743,627 UBE2Q2P10, LOC107986954, 40 more genes
    nsv7075262inversion1nstd229human GRCh38 chr8: 83,096,825-86,720,422 , GRCh37.p13 chr8: 84,009,060-87,732,650 REXO1L1P, LOC100422614, 54 more genes
    nsv7072230inversion1nstd229human GRCh38 chr8: 82,484,343-86,070,164 , GRCh37.p13 chr8: 83,396,578-87,082,393 CA2, LOC100533622, 44 more genes
    nsv6856034copy number variation1nstd229human GRCh38 chr8: 84,505,907-85,477,334 , GRCh37.p13 chr8: 85,418,142-86,389,563 LOC100422614, LOC105375933, 16 more genes
    nsv6855200copy number variation1nstd229human GRCh38 chr8: 85,118,701-85,125,700 , GRCh37.p13 chr8: 86,030,936-86,037,935 LRRCC1
    nsv6853456copy number variation1nstd229human GRCh38 chr8: 85,117,301-85,125,400 , GRCh37.p13 chr8: 86,029,536-86,037,635 LRRCC1
    nsv6852276copy number variation1nstd229human GRCh38 chr8: 82,628,086-85,182,488 , GRCh37.p13 chr8: 83,540,321-86,094,723 LRRCC1, PSMC2P2, 18 more genes
    nsv6849626copy number variation1nstd229human GRCh38 chr8: 85,125,101-85,126,700 , GRCh37.p13 chr8: 86,037,336-86,038,935 LRRCC1
    nsv6840017copy number variation1nstd229human GRCh38 chr8: 85,099,696-85,541,973 , GRCh37.p13 chr8: 86,011,931-86,454,202 RBIS, CA2, 10 more genes
    nsv6839219copy number variation1nstd229human GRCh38 chr8: 84,866,392-85,123,951 , GRCh37.p13 chr8: 85,778,627-86,036,186 JCHAINP1, RALYL, 4 more genes
    nsv6637670copy number variation1nstd102humanUncertain significance GRCh37 chr8: 83,705,217-86,441,492 , GRCh38.p12 chr8: 82,792,982-85,529,263 CA13, LOC100420845, 24 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6560109inversion1nstd223human GRCh38 chr8: 85,138,957-85,139,540 , GRCh37.p13 chr8: 86,051,192-86,051,775 LRRCC1
    nsv6429260copy number variation1nstd223human GRCh38 chr8: 85,143,002-85,145,269 , GRCh37.p13 chr8: 86,055,237-86,057,504 LRRCC1
    nsv6428289copy number variation1nstd223human GRCh38 chr8: 85,096,801-85,185,900 , GRCh37.p13 chr8: 86,009,036-86,098,135 E2F5, E2F5-DT, 2 more genes
    nsv6427756copy number variation1nstd223human GRCh38 chr8: 85,115,010-85,115,648 , GRCh37.p13 chr8: 86,027,245-86,027,883 LRRCC1
    nsv6425699copy number variation1nstd223human GRCh38 chr8: 82,628,086-85,182,486 , GRCh37.p13 chr8: 83,540,321-86,094,721 JCHAINP1, LINC01419, 18 more genes
    nsv6421370copy number variation1nstd223human GRCh38 chr8: 85,117,201-85,118,500 , GRCh37.p13 chr8: 86,029,436-86,030,735 LRRCC1
    nsv6418167copy number variation1nstd223human GRCh38 chr8: 85,118,699-85,125,732 , GRCh37.p13 chr8: 86,030,934-86,037,967 LRRCC1
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