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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7058053inversion1nstd229human GRCh38 chr6: 12,061,960-18,307,388 , GRCh37.p13 chr6: 12,062,193-18,307,619 RNU7-133P, CAP2, 87 more genes
    nsv7055214inversion1nstd229human GRCh38 chr6: 13,924,594-13,924,642 , GRCh37.p13 chr6: 13,924,825-13,924,873 RNF182
    nsv7054969inversion1nstd229human GRCh38 chr6: 13,881,274-14,018,794 , GRCh37.p13 chr6: 13,881,505-14,019,025 MRPL35P1, RNF182
    nsv7052250inversion1nstd229human GRCh38 chr6: 11,964,842-17,051,222 , GRCh37.p13 chr6: 11,965,075-17,051,453 LINC02543, ARPC3P5, 66 more genes
    nsv7051552inversion1nstd229human GRCh38 chr6: 11,086,774-14,472,374 , GRCh37.p13 chr6: 11,087,007-14,472,605 LOC105374933, ADTRP, 53 more genes
    nsv7049155inversion1nstd229human GRCh38 chr6: 13,950,791-13,954,114 , GRCh37.p13 chr6: 13,951,022-13,954,345 RNF182
    nsv7048416inversion1nstd229human GRCh38 chr6: 13,974,407-13,974,465 , GRCh37.p13 chr6: 13,974,638-13,974,696 RNF182
    nsv7045672inversion1nstd229human GRCh38 chr6: 13,954,856-13,978,858 , GRCh37.p13 chr6: 13,955,087-13,979,089 RNF182
    nsv6795520copy number variation1nstd229human GRCh38 chr6: 13,925,548-13,935,533 , GRCh37.p13 chr6: 13,925,779-13,935,764 RNF182
    nsv6790753copy number variation1nstd229human GRCh38 chr6: 13,928,609-13,940,337 , GRCh37.p13 chr6: 13,928,840-13,940,568 RNF182
    nsv6784283copy number variation1nstd229human GRCh38 chr6: 13,906,801-13,961,900 , GRCh37.p13 chr6: 13,907,032-13,962,131 RNF182, MRPL35P1
    nsv6783143copy number variation1nstd229human GRCh38 chr6: 13,970,580-14,047,459 , GRCh37.p13 chr6: 13,970,811-14,047,690 RNF182
    nsv6778971copy number variation1nstd229human GRCh38 chr6: 13,965,201-13,974,200 , GRCh37.p13 chr6: 13,965,432-13,974,431 RNF182
    nsv6778396copy number variation1nstd229human GRCh38 chr6: 13,240,748-15,495,244 , GRCh37.p13 chr6: 13,240,980-15,495,475 MRPL35P1, LOC105374938, 34 more genes
    nsv6637057copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 13,891,547-15,718,444 , GRCh38.p12 chr6: 13,891,316-15,718,213 JARID2, CD83, 22 more genes
    nsv6636333copy number variation1nstd102humanPathogenic GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418 SOX4, MDH1P2, 136 more genes
    nsv6630850copy number variation1nstd224human GRCh37 chr6: 13,921,016-15,281,454 , GRCh38.p12 chr6: 13,920,785-15,281,223 RNF182, LINC01108, 17 more genes
    nsv6565072inversion1nstd223human GRCh38 chr6: 11,964,842-17,051,222 , GRCh37.p13 chr6: 11,965,075-17,051,453 GMPR, LOC105374933, 66 more genes
    nsv6414141copy number variation1nstd223human GRCh38 chr6: 13,979,901-13,982,000 , GRCh37.p13 chr6: 13,980,132-13,982,231 RNF182
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