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Items: 1 to 20 of 430

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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
    nsv7066841inversion1nstd229human GRCh38 chr8: 94,144,698-94,144,783 , GRCh37.p13 chr8: 95,156,926-95,157,011 CDH17, LOC105375647
    nsv6857581copy number variation1nstd229human GRCh38 chr8: 94,203,595-94,208,172 , GRCh37.p13 chr8: 95,215,823-95,220,400 CDH17
    nsv6856811copy number variation1nstd229human GRCh38 chr8: 94,165,859-94,166,057 , GRCh37.p13 chr8: 95,178,087-95,178,285 CDH17
    nsv6856580copy number variation1nstd229human GRCh38 chr8: 94,184,427-94,186,828 , GRCh37.p13 chr8: 95,196,655-95,199,056 CDH17
    nsv6853734copy number variation1nstd229human GRCh38 chr8: 94,172,267-94,287,421 , GRCh37.p13 chr8: 95,184,495-95,299,649 LOC105375648, RPL6P23, 2 more genes
    nsv6853608copy number variation1nstd229human GRCh38 chr8: 94,217,139-94,220,290 , GRCh37.p13 chr8: 95,229,367-95,232,518 CDH17
    nsv6853214copy number variation1nstd229human GRCh38 chr8: 94,184,901-94,281,700 , GRCh37.p13 chr8: 95,197,129-95,293,928 LOC105375648, CDH17, 2 more genes
    nsv6852656copy number variation1nstd229human GRCh38 chr8: 93,809,901-94,281,700 , GRCh37.p13 chr8: 94,822,129-95,293,928 MYL12AP1, LOC105375648, 9 more genes
    nsv6849997copy number variation1nstd229human GRCh38 chr8: 94,210,802-94,212,815 , GRCh37.p13 chr8: 95,223,030-95,225,043 CDH17
    nsv6848428copy number variation1nstd229human GRCh38 chr8: 94,169,605-94,177,084 , GRCh37.p13 chr8: 95,181,833-95,189,312 CDH17
    nsv6847900copy number variation1nstd229human GRCh38 chr8: 94,152,799-94,184,101 , GRCh37.p13 chr8: 95,165,027-95,196,329 CDH17
    nsv6846629copy number variation1nstd229human GRCh38 chr8: 93,895,507-94,241,144 , GRCh37.p13 chr8: 94,907,735-95,253,372 MIR378D2, RPL34P18, 6 more genes
    nsv6840584copy number variation1nstd229human GRCh38 chr8: 94,200,575-95,023,354 , GRCh37.p13 chr8: 95,212,803-96,035,582 NDUFAF6, FSBP, 18 more genes
    nsv6840171copy number variation1nstd229human GRCh38 chr8: 94,156,321-94,159,966 , GRCh37.p13 chr8: 95,168,549-95,172,194 CDH17
    nsv6838883copy number variation1nstd229human GRCh38 chr8: 93,807,501-94,427,400 , GRCh37.p13 chr8: 94,819,729-95,439,628 LOC105375647, RPL6P23, 13 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
    nsv6561984inversion1nstd223human GRCh38 chr8: 94,195,245-94,197,296 , GRCh37.p13 chr8: 95,207,473-95,209,524 CDH17
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