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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5132478mobile element insertion1nstd203human GRCh38 chr10: 13,530,255-13,530,255 , GRCh37.p13 chr10: 13,572,255-13,572,255 BEND7-DT
    nsv4975023copy number variation1nstd200human GRCh38 chr10: 13,517,223-13,530,456 , GRCh37.p13 chr10: 13,559,223-13,572,456 BEND7-DT, BEND7
    nsv4975022copy number variation1nstd200human GRCh38 chr10: 13,516,027-13,534,132 , GRCh37.p13 chr10: 13,558,027-13,576,132 BEND7, BEND7-DT
    nsv4844813copy number variation1nstd200human GRCh37 chr10: 13,558,027-13,576,132 , GRCh38.p12 chr10: 13,516,027-13,534,132 BEND7, BEND7-DT
    nsv4842483copy number variation1nstd200human GRCh37 chr10: 13,559,223-13,572,456 , GRCh38.p12 chr10: 13,517,223-13,530,456 BEND7-DT, BEND7
    nsv4615368copy number variation1nstd183human GRCh37 chr10: 13,570,475-13,571,415 , GRCh38.p12 chr10: 13,528,475-13,529,415 BEND7-DT, BEND7
    nsv4604854copy number variation1nstd183human GRCh37 chr10: 13,570,056-13,571,415 , GRCh38.p12 chr10: 13,528,056-13,529,415 BEND7, BEND7-DT
    nsv4455628copy number variation1nstd102humanUncertain significance GRCh37 chr10: 13,551,991-13,716,316 , GRCh38.p12 chr10: 13,509,991-13,674,316 FRMD4A, LOC105376422, 4 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4455478copy number variation1nstd102humanUncertain significance GRCh37 chr10: 13,469,262-13,747,769 , GRCh38.p12 chr10: 13,427,262-13,705,769 BEND7, RPL6P24, 4 more genes
    nsv4428342copy number variation1nstd174human GRCh37 chr10: 13,570,056-13,571,415 , GRCh38.p12 chr10: 13,528,056-13,529,415 BEND7, BEND7-DT
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv3924406copy number variation1nstd102humanPathogenic GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982 WDR37, LOC105376364, 302 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
    nsv3920598copy number variation1nstd102humanBenign NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169 LOC100420467, LOC105376474, 709 more genes
    nsv3920285copy number variation1nstd102humanPathogenic NCBI36 chr10: 106,418-15,455,341 , GRCh37.p13 chr10: 116,418-15,415,335 , GRCh38.p12 chr10: 70,478-15,373,336 NRBF2P5, DDX20P1, 265 more genes
    nsv3918372copy number variation1nstd102humanPathogenic GRCh38 chr10: 70,478-13,736,564 , GRCh37 chr10: 224,406-13,778,564 , NCBI36 chr10: 106,418-13,818,570 IL9RP2, PRKCQ, 232 more genes
    nsv3917667copy number variation1nstd102humanPathogenic GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913 RN7SKP241, DIP2C-AS1, 389 more genes
    nsv3914771copy number variation1nstd102humanPathogenic GRCh38 chr10: 54,086-19,336,980 , NCBI36 chr10: 90,026-19,665,915 , GRCh37 chr10: 100,026-19,625,909 COX6CP17, TUBAL3, 302 more genes
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