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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961200insertion1nstd209human GRCh38 chr1: 156,817,047-156,817,047 , GRCh37.p13 chr1: 156,786,839-156,786,839 NTRK1, SH2D2A
    nsv5883322copy number variation1nstd209human GRCh38 chr1: 156,824,925-156,829,686 , GRCh37.p13 chr1: 156,794,717-156,799,478 NTRK1
    nsv5872704copy number variation1nstd209human GRCh38 chr1: 156,836,732-156,836,783 , GRCh37.p13 chr1: 156,806,524-156,806,575 NTRK1
    nsv5828365copy number variation1nstd209human GRCh38 chr1: 156,824,820-156,829,467 , GRCh37.p13 chr1: 156,794,612-156,799,259 NTRK1
    nsv5613803insertion1nstd207human GRCh38 chr1: 156,827,078-156,827,078 , GRCh37.p13 chr1: 156,796,870-156,796,870 NTRK1
    nsv5569410copy number variation1nstd207human GRCh38 chr1: 156,836,732-156,836,783 , GRCh37.p13 chr1: 156,806,524-156,806,575 NTRK1
    nsv5543227insertion1nstd206human GRCh38 chr1: 156,827,078-156,827,078 , GRCh37.p13 chr1: 156,796,870-156,796,870 NTRK1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5381062copy number variation1nstd102humanUncertain significance GRCh37 chr1: 156,834,510-156,834,601 , GRCh38.p12 chr1: 156,864,718-156,864,809 NTRK1
    nsv5165834mobile element insertion1nstd203human GRCh38 chr1: 156,835,440-156,835,448 , GRCh37.p13 chr1: 156,805,232-156,805,240 NTRK1
    nsv5064514mobile element insertion1nstd203human GRCh38 chr1: 156,827,078-156,827,100 , GRCh37.p13 chr1: 156,796,870-156,796,892 NTRK1
    nsv4897607copy number variation1nstd200human GRCh38 chr1: 156,854,077-156,868,731 , GRCh37.p13 chr1: 156,823,869-156,838,523 INSRR, NTRK1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4742656copy number variation1nstd199human GRCh37 chr1: 156,806,537-156,806,589 , GRCh38.p12 chr1: 156,836,745-156,836,797 NTRK1
    nsv4683948copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 156,834,818-156,837,900 , GRCh38 chr1: 156,865,026-156,868,108 NTRK1
    nsv4579749copy number variation1nstd183human GRCh37 chr1: 156,837,893-156,838,611 , GRCh38.p12 chr1: 156,868,101-156,868,819 NTRK1
    nsv4533857insertion1nstd166human GRCh37.p13 chr1: 156,796,870-156,796,870 , GRCh38.p12 chr1: 156,827,078-156,827,078 NTRK1
    nsv4389284copy number variation1nstd171human GRCh37 chr1: 156,831,061-156,831,091 , GRCh38.p12 chr1: 156,861,269-156,861,299 NTRK1
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
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