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Items: 1 to 20 of 137

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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
    nsv6641783copy number variation1nstd229human GRCh38 chr1: 151,057,452-151,066,903 , GRCh37.p13 chr1: 151,029,928-151,039,379 MLLT11, CDC42SE1
    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
    nsv6329918copy number variation1nstd223human GRCh38 chr1: 151,069,636-151,069,937 , GRCh37.p13 chr1: 151,042,112-151,042,413 MLLT11, GABPB2
    nsv6326491copy number variation1nstd223human GRCh38 chr1: 151,059,176-151,060,451 , GRCh37.p13 chr1: 151,031,652-151,032,927 MLLT11, CDC42SE1
    nsv6324194copy number variation1nstd223human GRCh38 chr1: 151,069,958-151,077,979 , GRCh37.p13 chr1: 151,042,434-151,050,455 MLLT11, GABPB2
    nsv6319974copy number variation1nstd223human GRCh38 chr1: 151,057,396-151,066,899 , GRCh37.p13 chr1: 151,029,872-151,039,375 MLLT11, CDC42SE1
    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
    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
    nsv5868766copy number variation1nstd209human GRCh38 chr1: 151,069,897-151,070,171 , GRCh37.p13 chr1: 151,042,373-151,042,647 MLLT11, GABPB2
    nsv5724252mobile element insertion1nstd211human GRCh38 chr1: 151,064,385-151,064,385 , GRCh37.p13 chr1: 151,036,861-151,036,861 MLLT11
    nsv5560892mobile element insertion1nstd206human GRCh38 chr1: 151,064,385-151,064,436 , GRCh37.p13 chr1: 151,036,861-151,036,912 MLLT11
    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
    nsv5212609copy number variation1nstd204human GRCh38.p13 chr1: 151,052,501-151,062,000 , GRCh37.p13 chr1: 151,024,977-151,034,476 MLLT11, CDC42SE1
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