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Items: 1 to 20 of 134

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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
    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
    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
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6314018copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,049,227-73,533,226 , GRCh38.p12 chr17: 75,053,132-75,537,145 MIF4GD-DT, TSEN54, 21 more genes
    nsv6291659copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,045,938-73,310,951 , GRCh38.p12 chr17: 75,049,843-75,314,870 SLC25A19, NUP85, 12 more genes
    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
    nsv5377665translocation1nstd200human GRCh38 chr17: 75,130,664-75,130,664 , GRCh38 chr4: 143,217,245-143,217,245 , GRCh37.p13 chr17: 73,126,759-73,126,759 , GRCh37.p13 chr4: 144,138,398-144,138,398 NT5C, ARMC7, 2 more genes
    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
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5014010copy number variation1nstd200human GRCh38 chr17: 75,062,121-75,491,883 , GRCh37.p13 chr17: 73,058,216-73,487,964 NUP85, RNU6-938P, 17 more genes
    nsv4858953copy number variation1nstd200human GRCh37 chr17: 73,124,280-73,124,977 , GRCh38.p12 chr17: 75,128,185-75,128,882 ARMC7, NT5C
    nsv4854385copy number variation1nstd200human GRCh37 chr17: 73,058,216-73,487,964 , GRCh38.p12 chr17: 75,062,121-75,491,883 LOC107985034, SUMO2, 17 more genes
    nsv4676145copy number variation1nstd102humanUncertain significance GRCh37 chr17: 72,945,415-73,414,786 , GRCh38.p12 chr17: 74,949,320-75,418,705 MIF4GD-DT, NT5C, 27 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4350658copy number variation1nstd102humanPathogenic GRCh37 chr17: 70,720,436-73,175,266 , GRCh38.p12 chr17: 72,724,297-75,179,171 HID1-AS1, CDR2L, 67 more genes
    nsv3972399copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942 AANAT, ACOX1, 243 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
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