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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv6641777copy number variation1nstd229human GRCh38 chr1: 150,967,801-151,307,200 , GRCh37.p13 chr1: 150,940,277-151,279,676 MINDY1, TNFAIP8L2, 23 more genes
    nsv6641764copy number variation1nstd229human GRCh38 chr1: 150,761,787-151,277,656 , GRCh37.p13 chr1: 150,734,263-151,250,132 VPS72, RPS29P29, 30 more genes
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6166407copy number variation1nstd214human GRCh38 chr1: 151,173,816-151,173,952 , GRCh37.p13 chr1: 151,146,292-151,146,428 TMOD4
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133733copy number variation1nstd213human GRCh37 chr1: 149,980,000-151,620,001 , GRCh38.p12 chr1: 150,008,051-151,647,525 CTSK, MCL1, 80 more genes
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 more genes
    nsv6133499copy number variation1nstd213human GRCh37 chr1: 149,880,000-153,720,001 , GRCh38.p12 chr1: 149,908,448-153,747,525 , CTSK, 198 more genes
    nsv5828134copy number variation1nstd209human GRCh38 chr1: 151,175,915-151,176,914 , GRCh37.p13 chr1: 151,148,391-151,149,390 VPS72, TMOD4
    nsv5416504copy number variation1nstd206human GRCh38 chr1: 151,167,908-151,168,738 , GRCh37.p13 chr1: 151,140,384-151,141,214 TMOD4, SCNM1, 1 more genes
    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
    nsv5381206copy number variation1nstd102humanUncertain significance GRCh37 chr1: 151,122,490-151,585,008 , GRCh38.p12 chr1: 151,150,014-151,612,532 CGN, ZNF687-AS1, 21 more genes
    nsv4897366copy number variation1nstd200human GRCh38 chr1: 151,173,913-151,180,968 , GRCh37.p13 chr1: 151,146,389-151,153,444 TMOD4, VPS72
    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
    nsv4712598copy number variation1nstd195human GRCh37 chr1: 151,042,151-151,571,701 , GRCh38.p12 chr1: 151,069,675-151,599,225 PI4KB, PSMD4, 24 more genes
    nsv4368436copy number variation1nstd173human GRCh37 chr1: 151,144,910-151,243,214 , GRCh38.p12 chr1: 151,172,434-151,270,738 PSMD4, VPS72, 2 more genes
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