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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7044016inversion1nstd229human GRCh38 chr1: 92,106,711-92,128,080 , GRCh37.p13 chr1: 92,572,268-92,593,637 PRKAR1AP1, BTBD8, 1 more genes
    nsv6657319copy number variation1nstd229human GRCh38 chr1: 92,043,801-92,124,900 , GRCh37.p13 chr1: 92,509,358-92,590,457 EPHX4, GAPDHP46, 4 more genes
    nsv6657169copy number variation1nstd229human GRCh38 chr1: 91,926,801-92,147,900 , GRCh37.p13 chr1: 92,392,358-92,613,457 PRKAR1AP1, BRDT, 5 more genes
    nsv6657166copy number variation1nstd229human GRCh38 chr1: 91,834,471-92,124,019 , GRCh37.p13 chr1: 92,300,028-92,589,576 PRKAR1AP1, BRDT, 6 more genes
    nsv6657157copy number variation1nstd229human GRCh38 chr1: 91,727,368-92,167,312 , GRCh37.p13 chr1: 92,192,925-92,632,869 TGFBR3, PRKAR1AP1, 7 more genes
    nsv6657085copy number variation1nstd229human GRCh38 chr1: 91,692,426-92,198,352 , GRCh37.p13 chr1: 92,157,983-92,663,909 BTBD8, BRDT, 7 more genes
    nsv6656286copy number variation1nstd229human GRCh38 chr1: 91,753,971-92,209,756 , GRCh37.p13 chr1: 92,219,528-92,675,313 TGFBR3, LOC100419803, 8 more genes
    nsv6656285copy number variation1nstd229human GRCh38 chr1: 91,749,866-92,170,286 , GRCh37.p13 chr1: 92,215,423-92,635,843 PRKAR1AP1, BRDT, 7 more genes
    nsv6636250copy number variation1nstd102humanUncertain significance GRCh37 chr1: 92,157,808-92,714,991 , GRCh38.p12 chr1: 91,692,251-92,249,434 RN7SL653P, SETSIP, 11 more genes
    nsv6626483copy number variation1nstd224human GRCh37 chr1: 92,224,815-92,633,442 , GRCh38.p12 chr1: 91,759,258-92,167,885 BRDT, PRKAR1AP1, 7 more genes
    nsv6626296copy number variation1nstd224human GRCh37 chr1: 92,441,876-92,595,338 , GRCh38.p12 chr1: 91,976,319-92,129,781 BRDT, PRKAR1AP1, 5 more genes
    nsv6334739copy number variation1nstd223human GRCh38 chr1: 91,095,691-93,048,861 , GRCh37.p13 chr1: 91,561,248-93,514,418 LOC107985417, BRDT, 38 more genes
    nsv6321748copy number variation1nstd223human GRCh38 chr1: 91,744,926-92,193,821 , GRCh37.p13 chr1: 92,210,483-92,659,378 BRDT, EPHX4, 7 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv6134256copy number variation1nstd213human GRCh37 chr1: 92,400,000-92,630,001 , GRCh38.p12 chr1: 91,934,443-92,164,444 BRDT, PRKAR1AP1, 5 more genes
    nsv4903765copy number variation1nstd200human GRCh38 chr1: 91,864,941-92,131,489 , GRCh37.p13 chr1: 92,330,498-92,597,046 PRKAR1AP1, LPCAT2BP, 6 more genes
    nsv4903764copy number variation1nstd200human GRCh38 chr1: 91,820,583-92,212,428 , GRCh37.p13 chr1: 92,286,140-92,677,985 PRKAR1AP1, BRDT, 8 more genes
    nsv4903763copy number variation1nstd200human GRCh38 chr1: 91,767,165-92,168,213 , GRCh37.p13 chr1: 92,232,722-92,633,770 PRKAR1AP1, TGFBR3, 7 more genes
    nsv4903762copy number variation1nstd200human GRCh38 chr1: 91,749,866-92,170,286 , GRCh37.p13 chr1: 92,215,423-92,635,843 PRKAR1AP1, TGFBR3, 7 more genes
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