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Items: 1 to 20 of 159

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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
    nsv7095751copy number variation1nstd102humanUncertain significance GRCh37 chr1: 150,524,765-150,532,672 , GRCh38.p12 chr1: 150,552,289-150,560,196 ADAMTSL4-AS2, ADAMTSL4-AS1, 2 more genes
    nsv7095244copy number variation1nstd102humanUncertain significance GRCh37 chr1: 150,524,765-150,525,096 , GRCh38.p12 chr1: 150,552,289-150,552,620 MIR4257, ADAMTSL4-AS2, 1 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
    nsv6641920copy number variation1nstd229human GRCh38 chr1: 150,557,287-150,558,020 , GRCh37.p13 chr1: 150,529,763-150,530,496 ADAMTSL4
    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
    nsv6315000delins1nstd102humanLikely pathogenic GRCh38 chr1: 150,558,562-150,558,694 , GRCh37 chr1: 150,531,038-150,531,170 ADAMTSL4
    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
    nsv6152319copy number variation1nstd214human GRCh38 chr1: 150,549,058-150,549,142 , GRCh37.p13 chr1: 150,521,534-150,521,618 ADAMTSL4-AS2, ADAMTSL4
    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
    nsv5981282copy number variation1nstd212human GRCh38 chr1: 150,549,100-150,549,183 , GRCh37.p13 chr1: 150,521,576-150,521,659 ADAMTSL4, ADAMTSL4-AS2
    nsv5877231copy number variation1nstd209human GRCh38 chr1: 150,549,099-150,549,183 , GRCh37.p13 chr1: 150,521,575-150,521,659 ADAMTSL4, ADAMTSL4-AS2
    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
    nsv5216860copy number variation1nstd204human GRCh38.p13 chr1: 150,560,984-150,561,983 , GRCh37.p13 chr1: 150,533,460-150,534,459 ADAMTSL4, ADAMTSL4-AS1
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