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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052191inversion1nstd229human GRCh38 chr6: 48,907,228-49,062,541 , GRCh37.p13 chr6: 48,874,865-49,030,178 PRR11P1
    nsv7051257inversion1nstd229human GRCh38 chr6: 48,635,017-48,962,784 , GRCh37.p13 chr6: 48,602,753-48,930,421 PRR11P1
    nsv7047757inversion1nstd229human GRCh38 chr6: 48,907,112-49,069,917 , GRCh37.p13 chr6: 48,874,749-49,037,554 PRR11P1
    nsv7047571inversion1nstd229human GRCh38 chr6: 47,471,816-49,526,857 , GRCh37.p13 chr6: 47,439,552-49,494,570 MMUT, RN7SKP116, 19 more genes
    nsv7042763inversion1nstd229human GRCh38 chr6: 48,144,831-49,003,789 , GRCh37.p13 chr6: 48,112,567-48,971,426 RBMXP1, PRR11P1, 2 more genes
    nsv7039058inversion1nstd229human GRCh38 chr6: 48,833,100-49,063,004 , GRCh37.p13 chr6: 48,800,737-49,030,641 PRR11P1
    nsv6796759copy number variation1nstd229human GRCh38 chr6: 48,818,356-49,130,038 , GRCh37.p13 chr6: 48,785,993-49,097,674 LOC100421158, PRR11P1
    nsv6795749copy number variation1nstd229human GRCh38 chr6: 48,881,401-48,969,800 , GRCh37.p13 chr6: 48,849,038-48,937,437 PRR11P1
    nsv6789367copy number variation1nstd229human GRCh38 chr6: 48,645,525-49,878,656 , GRCh37.p13 chr6: 48,613,261-49,846,369 LOC100421158, CYP2AC1P, 14 more genes
    nsv6788745copy number variation1nstd229human GRCh38 chr6: 48,938,001-48,969,800 , GRCh37.p13 chr6: 48,905,638-48,937,437 PRR11P1
    nsv6788138copy number variation1nstd229human GRCh38 chr6: 48,932,932-48,979,611 , GRCh37.p13 chr6: 48,900,569-48,947,248 PRR11P1
    nsv6784560copy number variation1nstd229human GRCh38 chr6: 48,951,966-48,959,500 , GRCh37.p13 chr6: 48,919,603-48,927,137 PRR11P1
    nsv6784087copy number variation1nstd229human GRCh38 chr6: 48,839,700-48,961,950 , GRCh37.p13 chr6: 48,807,337-48,929,587 PRR11P1
    nsv6780029copy number variation1nstd229human GRCh38 chr6: 48,870,993-48,969,636 , GRCh37.p13 chr6: 48,838,630-48,937,273 PRR11P1
    nsv6779879copy number variation1nstd229human GRCh38 chr6: 48,939,401-48,969,800 , GRCh37.p13 chr6: 48,907,038-48,937,437 PRR11P1
    nsv6630998copy number variation1nstd224human GRCh37 chr6: 48,812,682-49,020,666 , GRCh38.p12 chr6: 48,845,045-49,053,029 PRR11P1
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5892977copy number variation1nstd209human GRCh38 chr6: 48,907,542-49,076,261 , GRCh37.p13 chr6: 48,875,179-49,043,898 PRR11P1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
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