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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097614copy number variation1nstd102humanUncertain significance GRCh37 chr7: 16,131,320-17,382,688 , GRCh38.p12 chr7: 16,091,695-17,343,064 BRWD1P3, ANKMY2, 19 more genes
    nsv7038576inversion1nstd229human GRCh38 chr7: 16,300,700-17,558,371 , GRCh37.p13 chr7: 16,340,325-17,597,995 LOC317727, LOC105375170, 21 more genes
    nsv6817059copy number variation1nstd229human GRCh38 chr7: 16,477,104-16,531,501 , GRCh37.p13 chr7: 16,516,729-16,571,126 LRRC72
    nsv6815095copy number variation1nstd229human GRCh38 chr7: 16,549,946-16,558,374 , GRCh37.p13 chr7: 16,589,571-16,597,999 LRRC72
    nsv6810871copy number variation1nstd229human GRCh38 chr7: 16,504,503-17,165,581 , GRCh37.p13 chr7: 16,544,128-17,205,205 LRRC72, LOC105375169, 13 more genes
    nsv6804759copy number variation1nstd229human GRCh38 chr7: 16,528,001-16,536,700 , GRCh37.p13 chr7: 16,567,626-16,576,325 LRRC72
    nsv6802806copy number variation1nstd229human GRCh38 chr7: 16,542,601-16,652,700 , GRCh37.p13 chr7: 16,582,226-16,692,325 LRRC72, ANKMY2, 3 more genes
    nsv6799404copy number variation1nstd229human GRCh38 chr7: 16,359,233-17,380,982 , GRCh37.p13 chr7: 16,398,858-17,420,606 LOC101927609, SOSTDC1, 19 more genes
    nsv6798940copy number variation1nstd229human GRCh38 chr7: 16,506,301-16,533,100 , GRCh37.p13 chr7: 16,545,926-16,572,725 LRRC72
    nsv6798562copy number variation1nstd229human GRCh38 chr7: 16,560,906-16,566,024 , GRCh37.p13 chr7: 16,600,531-16,605,649 LRRC72
    nsv6798222copy number variation1nstd229human GRCh38 chr7: 16,522,318-16,547,902 , GRCh37.p13 chr7: 16,561,943-16,587,527 LRRC72
    nsv6637135copy number variation1nstd102humanUncertain significance GRCh37 chr7: 15,639,869-16,963,424 , GRCh38.p12 chr7: 15,600,244-16,923,800 LOC105375166, LOC105375169, 20 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631613copy number variation1nstd224human GRCh37 chr7: 16,605,357-16,847,745 , GRCh38.p12 chr7: 16,565,732-16,808,121 AGR2, TSPAN13, 5 more genes
    nsv6631612copy number variation1nstd224human GRCh37 chr7: 16,500,142-17,040,226 , GRCh38.p12 chr7: 16,460,517-17,000,602 RAD17P1, LOC105375169, 12 more genes
    nsv6619044copy number variation1nstd223human GRCh38 chr7: 16,566,501-16,568,000 , GRCh37.p13 chr7: 16,606,126-16,607,625 LRRC72
    nsv6618795copy number variation1nstd223human GRCh38 chr7: 16,563,107-16,563,582 , GRCh37.p13 chr7: 16,602,732-16,603,207 LRRC72
    nsv6615998copy number variation1nstd223human GRCh38 chr7: 16,527,901-16,536,700 , GRCh37.p13 chr7: 16,567,526-16,576,325 LRRC72
    nsv6614009copy number variation1nstd223human GRCh38 chr7: 16,572,701-16,574,700 , GRCh37.p13 chr7: 16,612,326-16,614,325 LRRC72
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