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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099231copy number variation1nstd231human GRCh38.p12 chr1: 149,962,894-151,006,586 , GRCh37 chr1: 149,934,818-150,979,062 ARNT, CTSK, 48 more genes
    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
    nsv6641923copy number variation1nstd229human GRCh38 chr1: 150,572,090-150,572,562 , GRCh37.p13 chr1: 150,544,566-150,545,038 MCL1, ADAMTSL4-AS1
    nsv6641916copy number variation1nstd229human GRCh38 chr1: 150,406,738-150,700,622 , GRCh37.p13 chr1: 150,440,214-150,673,098 RNU6-1042P, ENSA, 16 more genes
    nsv6641663copy number variation1nstd229human GRCh38 chr1: 150,478,701-150,603,000 , GRCh37.p13 chr1: 150,451,177-150,575,476 ECM1, LOC107985203, 10 more genes
    nsv6322618copy number variation1nstd223human GRCh38 chr1: 150,579,001-150,580,100 , GRCh37.p13 chr1: 150,551,477-150,552,576 MCL1, LOC107985203
    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
    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
    nsv4903843copy number variation1nstd200human GRCh38 chr1: 150,562,993-150,609,277 , GRCh37.p13 chr1: 150,535,469-150,581,753 RN7SL473P, RN7SL600P, 3 more genes
    nsv4903842copy number variation1nstd200human GRCh38 chr1: 150,406,738-150,700,622 , GRCh37.p13 chr1: 150,440,214-150,673,098 ADAMTSL4, ADAMTSL4-AS1, 16 more genes
    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
    nsv4712047copy number variation1nstd195human GRCh38.p12 chr1: 150,557,375-150,580,425 , GRCh37 chr1: 150,529,851-150,552,901 MCL1, ADAMTSL4, 4 more genes
    nsv4593945copy number variation1nstd183human GRCh37 chr1: 150,550,810-150,552,189 , GRCh38.p12 chr1: 150,578,334-150,579,713 MCL1, LOC107985203
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