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Items: 1 to 20 of 643

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146610insertion1nstd232human GRCh37.p13 chr1: 87,502,880-87,502,880 , GRCh38.p12 chr1: 87,037,197-87,037,197 HS2ST1
    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
    nsv7056564inversion1nstd229human GRCh38 chr1: 86,994,564-86,994,588 , GRCh37.p13 chr1: 87,460,247-87,460,271 HS2ST1
    nsv7051294inversion1nstd229human GRCh38 chr1: 87,053,484-87,053,586 , GRCh37.p13 chr1: 87,519,167-87,519,269 HS2ST1
    nsv7050787inversion1nstd229human GRCh38 chr1: 86,957,108-86,967,308 , GRCh37.p13 chr1: 87,422,791-87,432,991 HS2ST1
    nsv7049214inversion1nstd229human GRCh38 chr1: 86,481,973-88,243,863 , GRCh37.p13 chr1: 86,947,656-88,709,546 CLCA4, CLCA3P, 25 more genes
    nsv7046575inversion1nstd229human GRCh38 chr1: 83,069,893-89,051,563 , GRCh37.p13 chr1: 83,535,576-89,517,246 LOC105378826, RN7SL583P, 87 more genes
    nsv7041208inversion1nstd229human GRCh38 chr1: 86,888,533-88,519,414 , GRCh37.p13 chr1: 87,354,216-88,985,097 RNA5SP52, LINC01364, 17 more genes
    nsv6656699copy number variation1nstd229human GRCh38 chr1: 87,057,701-87,058,900 , GRCh37.p13 chr1: 87,523,384-87,524,583 HS2ST1
    nsv6656698copy number variation1nstd229human GRCh38 chr1: 87,048,086-87,048,264 , GRCh37.p13 chr1: 87,513,769-87,513,947 HS2ST1
    nsv6656697copy number variation1nstd229human GRCh38 chr1: 86,979,914-86,982,774 , GRCh37.p13 chr1: 87,445,597-87,448,457 HS2ST1
    nsv6656696copy number variation1nstd229human GRCh38 chr1: 86,963,809-86,963,872 , GRCh37.p13 chr1: 87,429,492-87,429,555 HS2ST1
    nsv6656695copy number variation1nstd229human GRCh38 chr1: 86,941,325-86,943,054 , GRCh37.p13 chr1: 87,407,008-87,408,737 HS2ST1
    nsv6656694copy number variation1nstd229human GRCh38 chr1: 86,925,047-86,929,456 , GRCh37.p13 chr1: 87,390,730-87,395,139 HS2ST1
    nsv6656693copy number variation1nstd229human GRCh38 chr1: 86,918,830-86,949,442 , GRCh37.p13 chr1: 87,384,513-87,415,125 HS2ST1
    nsv6656556copy number variation1nstd229human GRCh38 chr1: 87,074,201-87,079,900 , GRCh37.p13 chr1: 87,539,884-87,545,583 HS2ST1
    nsv6656555copy number variation1nstd229human GRCh38 chr1: 87,073,909-87,077,751 , GRCh37.p13 chr1: 87,539,592-87,543,434 HS2ST1
    nsv6656554copy number variation1nstd229human GRCh38 chr1: 87,042,489-87,048,791 , GRCh37.p13 chr1: 87,508,172-87,514,474 HS2ST1, LOC100421468, 1 more genes
    nsv6656552copy number variation1nstd229human GRCh38 chr1: 87,030,064-87,037,899 , GRCh37.p13 chr1: 87,495,747-87,503,582 HS2ST1
    nsv6656551copy number variation1nstd229human GRCh38 chr1: 87,009,337-87,016,040 , GRCh37.p13 chr1: 87,475,020-87,481,723 HS2ST1
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