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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942118copy number variation1nstd209human GRCh38 chr17: 74,774,804-74,775,108 , GRCh37.p13 chr17: 72,770,943-72,771,247 NAT9, TMEM104
    nsv5936469copy number variation1nstd209human GRCh38 chr17: 74,791,923-74,792,226 , GRCh37.p13 chr17: 72,788,062-72,788,365 TMEM104
    nsv5930890copy number variation1nstd209human GRCh38 chr17: 74,814,242-74,814,291 , GRCh37.p13 chr17: 72,810,381-72,810,430 TMEM104
    nsv5930338copy number variation1nstd209human GRCh38 chr17: 74,801,385-74,801,473 , GRCh37.p13 chr17: 72,797,524-72,797,612 TMEM104
    nsv5929884copy number variation1nstd209human GRCh38 chr17: 74,787,297-74,787,397 , GRCh37.p13 chr17: 72,783,436-72,783,536 TMEM104
    nsv5660966insertion1nstd207human GRCh38 chr17: 74,791,254-74,791,254 , GRCh37.p13 chr17: 72,787,393-72,787,393 TMEM104
    nsv5587885copy number variation1nstd207human GRCh38 chr17: 74,787,297-74,787,397 , GRCh37.p13 chr17: 72,783,436-72,783,536 TMEM104
    nsv5586819copy number variation1nstd207human GRCh38 chr17: 74,801,385-74,801,473 , GRCh37.p13 chr17: 72,797,524-72,797,612 TMEM104
    nsv5520084copy number variation1nstd206human GRCh38 chr17: 74,787,298-74,787,398 , GRCh37.p13 chr17: 72,783,437-72,783,537 TMEM104
    nsv5516198copy number variation1nstd206human GRCh38 chr17: 74,829,301-74,834,440 , GRCh37.p13 chr17: 72,825,440-72,830,579 TMEM104
    nsv5422263mobile element insertion1nstd206human GRCh38 chr17: 74,776,798-74,776,849 , GRCh37.p13 chr17: 72,772,937-72,772,988 NAT9, TMEM104
    nsv5294120copy number variation1nstd204human GRCh38.p13 chr17: 74,807,164-74,808,363 , GRCh37.p13 chr17: 72,803,303-72,804,502 TMEM104
    nsv5157499mobile element insertion1nstd203human GRCh38 chr17: 74,774,834-74,774,868 , GRCh37.p13 chr17: 72,770,973-72,771,007 NAT9, TMEM104
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5016647copy number variation1nstd200human GRCh38 chr17: 74,794,861-74,804,874 , GRCh37.p13 chr17: 72,791,000-72,801,013 TMEM104
    nsv5016646copy number variation1nstd200human GRCh38 chr17: 74,787,715-74,787,843 , GRCh37.p13 chr17: 72,783,854-72,783,982 TMEM104
    nsv4756665insertion1nstd199human GRCh37 chr17: 72,787,393-72,787,393 , GRCh38.p12 chr17: 74,791,254-74,791,254 TMEM104
    nsv4731665copy number variation1nstd199human GRCh37 chr17: 72,810,378-72,810,487 , GRCh38.p12 chr17: 74,814,239-74,814,348 TMEM104
    nsv4680241copy number variation1nstd189human GRCh37.p13 chr17: 71,821,655-72,788,501 , GRCh38.p12 chr17: 73,825,516-74,792,362 RPL38, NHERF1, 30 more genes
    nsv4679737copy number variation1nstd189human GRCh37.p13 chr17: 71,829,065-72,806,524 , GRCh38.p12 chr17: 73,832,926-74,810,385 RPL38, NHERF1, 29 more genes
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