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Items: 1 to 20 of 432

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137123copy number variation1nstd102humanPathogenic GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046 SLC26A7, LOC105375639, 112 more genes
    nsv7077999inversion1nstd229human GRCh38 chr8: 90,977,597-95,722,625 , GRCh37.p13 chr8: 91,989,825-96,734,853 LINC02894, MIR3150B, 70 more genes
    nsv7072578inversion1nstd229human GRCh38 chr8: 91,687,773-92,748,537 , GRCh37.p13 chr8: 92,700,001-93,760,765 FLJ46284, LOC105375638, 7 more genes
    nsv7071411inversion1nstd229human GRCh38 chr8: 92,018,830-92,022,093 , GRCh37.p13 chr8: 93,031,058-93,034,321 RUNX1T1
    nsv7066994inversion1nstd229human GRCh38 chr8: 92,036,235-92,036,292 , GRCh37.p13 chr8: 93,048,463-93,048,520 RUNX1T1
    nsv7065548inversion1nstd229human GRCh38 chr8: 91,994,997-91,995,064 , GRCh37.p13 chr8: 93,007,225-93,007,292 RUNX1T1
    nsv6857452copy number variation1nstd229human GRCh38 chr8: 92,037,664-92,041,728 , GRCh37.p13 chr8: 93,049,892-93,053,956 RUNX1T1
    nsv6857443copy number variation1nstd229human GRCh38 chr8: 92,033,701-92,042,500 , GRCh37.p13 chr8: 93,045,929-93,054,728 RUNX1T1
    nsv6857059copy number variation1nstd229human GRCh38 chr8: 92,075,401-92,079,200 , GRCh37.p13 chr8: 93,087,629-93,091,428 RUNX1T1
    nsv6848313copy number variation1nstd229human GRCh38 chr8: 92,090,073-92,090,739 , GRCh37.p13 chr8: 93,102,301-93,102,967 RUNX1T1
    nsv6843966copy number variation1nstd229human GRCh38 chr8: 92,046,407-92,081,934 , GRCh37.p13 chr8: 93,058,635-93,094,162 RUNX1T1
    nsv6842272copy number variation1nstd229human GRCh38 chr8: 92,047,731-92,047,762 , GRCh37.p13 chr8: 93,059,959-93,059,990 RUNX1T1
    nsv6841574copy number variation1nstd229human GRCh38 chr8: 92,024,248-92,028,680 , GRCh37.p13 chr8: 93,036,476-93,040,908 RUNX1T1
    nsv6840611copy number variation1nstd229human GRCh38 chr8: 91,976,826-91,980,034 , GRCh37.p13 chr8: 92,989,054-92,992,262 RUNX1T1
    nsv6838814copy number variation1nstd229human GRCh38 chr8: 91,948,384-91,953,768 , GRCh37.p13 chr8: 92,960,612-92,965,996 RUNX1T1
    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
    nsv6572931inversion1nstd223human GRCh38 chr8: 91,996,460-91,996,904 , GRCh37.p13 chr8: 93,008,688-93,009,132 RUNX1T1
    nsv6570670inversion1nstd223human GRCh38 chr8: 92,041,561-92,042,117 , GRCh37.p13 chr8: 93,053,789-93,054,345 RUNX1T1
    nsv6559722inversion1nstd223human GRCh38 chr8: 91,981,672-91,982,114 , GRCh37.p13 chr8: 92,993,900-92,994,342 RUNX1T1
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