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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7098900copy number variation1nstd102humanUncertain significance GRCh37 chr17: 72,864,876-73,328,878 , GRCh38.p12 chr17: 74,868,753-75,332,797 CDR2L, OTOP2, 28 more genes
    nsv7067736inversion1nstd229human GRCh38 chr17: 74,920,784-74,998,662 , GRCh37.p13 chr17: 72,916,879-72,994,757 CDR2L, USH1G, 4 more genes
    nsv6996002copy number variation1nstd229human GRCh38 chr17: 74,944,301-74,949,800 , GRCh37.p13 chr17: 72,940,396-72,945,895 HID1, OTOP3
    nsv6989448copy number variation1nstd229human GRCh38 chr17: 74,941,047-74,955,049 , GRCh37.p13 chr17: 72,937,142-72,951,144 OTOP3, HID1
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6983203copy number variation1nstd229human GRCh38 chr17: 74,947,301-74,949,500 , GRCh37.p13 chr17: 72,943,396-72,945,595 OTOP3, HID1
    nsv6980905copy number variation1nstd229human GRCh38 chr17: 74,674,101-75,023,500 , GRCh37.p13 chr17: 72,670,240-73,019,595 USH1G, NHERF1, 16 more genes
    nsv6978949copy number variation1nstd229human GRCh38 chr17: 74,730,301-75,013,700 , GRCh37.p13 chr17: 72,726,440-73,009,795 NAT9, GRIN2C, 14 more genes
    nsv6624308copy number variation1nstd224human GRCh37 chr17: 72,877,346-73,127,348 , GRCh38.p12 chr17: 74,881,216-75,131,253 SLC16A5, KCTD2, 18 more genes
    nsv6588805inversion1nstd223human GRCh38 chr17: 74,957,707-75,029,417 , GRCh37.p13 chr17: 72,953,802-73,025,512 MRPL58, CDR2L, 3 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6530686copy number variation1nstd223human GRCh38 chr17: 74,966,899-74,967,493 , GRCh37.p13 chr17: 72,962,994-72,963,588 HID1
    nsv6196618copy number variation1nstd214human GRCh38 chr17: 74,953,871-74,953,965 , GRCh37.p13 chr17: 72,949,966-72,950,060 HID1
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv5649388insertion1nstd207human GRCh38 chr17: 74,965,214-74,965,214 , GRCh37.p13 chr17: 72,961,309-72,961,309 HID1
    nsv5298973copy number variation1nstd204human GRCh38.p13 chr17: 74,951,501-75,212,200 , GRCh37.p13 chr17: 72,947,596-73,208,295 RNU6-362P, TRR-CCT2-1, 17 more genes
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5153229mobile element insertion1nstd203human GRCh38 chr17: 74,965,917-74,965,939 , GRCh37.p13 chr17: 72,962,012-72,962,034 HID1
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
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