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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933163copy number variation1nstd209human GRCh38 chr17: 69,215,768-69,242,040 , GRCh37.p13 chr17: 67,211,909-67,238,181 PRO1804, ABCA10
    nsv5869842copy number variation1nstd209human GRCh38 chr17: 69,215,745-69,237,949 , GRCh37.p13 chr17: 67,211,886-67,234,090 ABCA10, PRO1804
    nsv5518027copy number variation1nstd206human GRCh38 chr17: 68,893,715-69,642,424 , GRCh37.p13 chr17: 66,889,856-67,638,565 , ABCA10, 15 more genes
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv4729911copy number variation1nstd102humanUncertain significance GRCh37 chr17: 66,531,148-67,241,132 , GRCh38.p12 chr17: 68,535,007-69,244,991 SEC24AP1, PRKAR1A, 12 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
    nsv4380148copy number variation1nstd173human GRCh37 chr17: 67,205,358-67,239,706 , GRCh38.p12 chr17: 69,209,217-69,243,565 ABCA10, PRO1804, 1 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4252709copy number variation1nstd166human GRCh37.p13 chr17: 67,187,197-67,230,379 , GRCh38.p12 chr17: 69,191,056-69,234,238 ABCA10, PRO1804
    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
    nsv3921398copy number variation1nstd102humanPathogenic GRCh37 chr17: 65,829,982-68,081,995 , GRCh38 chr17: 67,833,866-70,085,854 , NCBI36 chr17: 63,260,444-65,593,590 LRRC37A16P, SNRPGP4, 41 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
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 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
    nsv3910890copy number variation1nstd102humanPathogenic GRCh38 chr17: 68,420,514-71,351,235 , NCBI36 chr17: 63,928,250-66,858,971 , GRCh37 chr17: 66,416,655-69,347,376 KCNJ16, LOC105371874, 34 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
    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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