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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976694inversion1nstd209human GRCh38 chr5: 179,854,164-180,408,925 , GRCh37.p13 chr5: 179,281,164-179,835,925 MAPK9, GFPT2, 11 more genes
    nsv5959409insertion1nstd209human GRCh38 chr5: 180,163,252-180,163,252 , GRCh37.p13 chr5: 179,590,252-179,590,252 RASGEF1C
    nsv5903329copy number variation1nstd209human GRCh38 chr5: 180,101,991-180,102,046 , GRCh37.p13 chr5: 179,528,991-179,529,046 RASGEF1C
    nsv5900777copy number variation1nstd209human GRCh38 chr5: 180,190,206-180,190,531 , GRCh37.p13 chr5: 179,617,206-179,617,531 RASGEF1C
    nsv5896068copy number variation1nstd209human GRCh38 chr5: 180,181,884-180,182,308 , GRCh37.p13 chr5: 179,608,884-179,609,308 RASGEF1C
    nsv5894686copy number variation1nstd209human GRCh38 chr5: 180,176,625-180,178,027 , GRCh37.p13 chr5: 179,603,625-179,605,027 RASGEF1C
    nsv5890532copy number variation1nstd209human GRCh38 chr5: 180,164,159-180,164,574 , GRCh37.p13 chr5: 179,591,159-179,591,574 RASGEF1C
    nsv5842262copy number variation1nstd209human GRCh38 chr5: 180,190,569-180,195,389 , GRCh37.p13 chr5: 179,617,569-179,622,389 RASGEF1C
    nsv5841954copy number variation1nstd209human GRCh38 chr5: 180,176,650-180,178,000 , GRCh37.p13 chr5: 179,603,650-179,605,000 RASGEF1C
    nsv5644162insertion3nstd207human GRCh38 chr5: 180,134,844-180,134,844 , GRCh37.p13 chr5: 179,561,844-179,561,844 RASGEF1C
    nsv5632290insertion1nstd207human GRCh38 chr5: 180,134,561-180,134,561 , GRCh37.p13 chr5: 179,561,561-179,561,561 RASGEF1C
    nsv5579590copy number variation1nstd207human GRCh38 chr5: 180,113,458-180,113,552 , GRCh37.p13 chr5: 179,540,458-179,540,552 RASGEF1C
    nsv5579221copy number variation1nstd207human GRCh38 chr5: 180,101,991-180,102,046 , GRCh37.p13 chr5: 179,528,991-179,529,046 RASGEF1C
    nsv5578772copy number variation1nstd207human GRCh38 chr5: 180,113,334-180,113,428 , GRCh37.p13 chr5: 179,540,334-179,540,428 RASGEF1C
    nsv5577040copy number variation1nstd207human GRCh38 chr5: 180,190,427-180,190,604 , GRCh37.p13 chr5: 179,617,427-179,617,604 RASGEF1C
    nsv5576933copy number variation1nstd207human GRCh38 chr5: 180,113,304-180,113,512 , GRCh37.p13 chr5: 179,540,304-179,540,512 RASGEF1C
    nsv5567544copy number variation1nstd207human GRCh38 chr5: 180,113,117-180,113,192 , GRCh37.p13 chr5: 179,540,117-179,540,192 RASGEF1C
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5549025insertion1nstd206human GRCh38 chr5: 180,209,134-180,209,167 , GRCh37.p13 chr5: 179,636,134-179,636,167 RASGEF1C
    nsv5545896insertion1nstd206human GRCh38 chr5: 180,185,603-180,185,613 , GRCh37.p13 chr5: 179,612,603-179,612,613 RASGEF1C
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