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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 LOC101928447, GRB2, 368 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3909523copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062 RPL38, RNF157-AS1, 428 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 more genes
    nsv3907936copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,057,756-73,429,731 , GRCh38.p12 chr17: 75,061,661-75,433,650 ARMC7, MRPS7, 16 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
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