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Items: 1 to 20 of 21

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6310732copy number variation1nstd102humanPathogenic GRCh37 chr1: 156,837,886-156,841,557 , GRCh38.p12 chr1: 156,868,094-156,871,765 NTRK1
    nsv3875204copy number variation1nstd102humanPathogenic GRCh37 chr1: 156,844,810-156,846,190 , GRCh38 chr1: 156,875,018-156,876,398 NTRK1
    nsv4683948copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 156,834,818-156,837,900 , GRCh38 chr1: 156,865,026-156,868,108 NTRK1
    nsv6310525copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 156,837,886-156,843,392 , GRCh38.p12 chr1: 156,868,094-156,873,600 NTRK1
    nsv5381062copy number variation1nstd102humanUncertain significance GRCh37 chr1: 156,834,510-156,834,601 , GRCh38.p12 chr1: 156,864,718-156,864,809 NTRK1
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 NTRK1, CRB1, 1608 more genes
    nsv3882925copy number variation1nstd102humanPathogenic GRCh37 chr1: 155,636,337-158,024,499 , GRCh38.p12 chr1: 155,666,546-158,054,709 NTRK1, SH2D2A, 88 more genes
    nsv6310593copy number variation1nstd102humanPathogenic GRCh37 chr1: 155,581,953-156,851,434 , GRCh38.p12 chr1: 155,612,162-156,881,642 NTRK1, MIR9-1, 62 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 NTRK1, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 NTRK1, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 NTRK1, RNU1-153P, 4887 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 NTRK1, LOC101060227, 1608 more genes
    nsv3900459copy number variation1nstd102humanPathogenic GRCh38 chr1: 149,854,269-180,267,197 , NCBI36 chr1: 148,092,455-178,502,955 , GRCh37 chr1: 149,825,831-180,236,332 NTRK1, HORMAD1, 923 more genes
    nsv3917016copy number variation1nstd102humanPathogenic NCBI36 chr1: 152,220,775-155,340,341 , GRCh37.p13 chr1: 153,954,151-157,073,717 , GRCh38.p12 chr1: 153,981,675-157,103,925 NTRK1, SMU1P1, 152 more genes
    nsv3906950copy number variation1nstd102humanPathogenic GRCh38 chr1: 154,566,501-157,624,084 , NCBI36 chr1: 152,805,601-155,860,498 , GRCh37 chr1: 154,538,977-157,593,874 NTRK1, ARHGEF2-AS2, 131 more genes
    nsv3909898inversion1nstd102humanLikely pathogenic GRCh38.p12 chr1: 154,158,509-156,874,085 , GRCh37 chr1: 154,130,985-156,843,877 NTRK1, ADAR, 136 more genes
    nsv6290596copy number variation1nstd102humanUncertain significance GRCh37 chr1: 156,665,257-156,902,706 , GRCh38.p12 chr1: 156,695,465-156,932,914 NTRK1, ISG20L2, 10 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 NTRK1, DCST1, 2428 more genes
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 NTRK1, PRPF3, 352 more genes
    nsv6310523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,141,761-156,851,434 , GRCh38.p12 chr1: 154,169,285-156,881,642 NTRK1, MIR555, 135 more genes
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