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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5833155copy number variation1nstd209human GRCh38 chr2: 273,798-284,197 , GRCh37.p13 chr2: 273,798-284,197 ALKAL2, ACP1
    nsv5833152copy number variation1nstd209human GRCh38 chr2: 261,648-267,447 , GRCh37.p13 chr2: 261,648-267,447 SH3YL1, ACP1
    nsv5442514copy number variation1nstd206human GRCh38 chr2: 252,077-294,598 , GRCh37.p13 chr2: 252,077-294,598 LOC101927262, LOC105373346, 3 more genes
    nsv4904659copy number variation1nstd200human GRCh38 chr2: 197,015-655,136 , GRCh37.p13 chr2: 197,015-655,136 ACP1, SH3YL1, 9 more genes
    nsv4904657copy number variation1nstd200human GRCh38 chr2: 132,469-641,802 , GRCh37.p13 chr2: 132,469-641,802 SH3YL1, LOC105373324, 10 more genes
    nsv4891929copy number variation1nstd200human GRCh38 chr2: 260,946-263,131 , GRCh37.p13 chr2: 260,946-263,131 ACP1, SH3YL1
    nsv4728591copy number variation1nstd102humanUncertain significance GRCh37 chr2: 12,770-1,126,253 , GRCh38.p12 chr2: 12,770-1,130,567 LOC105373351, LINC01875, 20 more genes
    nsv4728447copy number variation1nstd102humanLikely benign GRCh37 chr2: 210,211-262,993 , GRCh38.p12 chr2: 210,211-262,993 ACP1, SH3YL1
    nsv4728162copy number variation1nstd102humanUncertain significance GRCh37 chr2: 12,770-1,680,334 , GRCh38.p12 chr2: 12,770-1,676,562 LINC01874, LOC105373346, 24 more genes
    nsv4712928copy number variation1nstd195human GRCh37 chr2: 236,351-306,851 , GRCh38.p12 chr2: 236,351-306,851 ACP1, SH3YL1, 3 more genes
    nsv4674286copy number variation1nstd102humanLikely benign GRCh37 chr2: 275,774-397,593 , GRCh38.p12 chr2: 275,774-397,593 ACP1, ALKAL2, 4 more genes
    nsv4674039copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-3,000,954 , GRCh38.p12 chr2: 12,770-2,997,182 LINC01115, LOC105373352, 31 more genes
    nsv4595480copy number variation1nstd183human GRCh37 chr2: 264,086-264,879 , GRCh38.p12 chr2: 264,086-264,879 ACP1, SH3YL1
    nsv4585727copy number variation1nstd183human GRCh37 chr2: 264,775-264,879 , GRCh38.p12 chr2: 264,775-264,879 ACP1, SH3YL1
    nsv4584365copy number variation1nstd183human GRCh37 chr2: 66,097-287,353 , GRCh38.p12 chr2: 66,097-287,353 SH3YL1, ALKAL2, 3 more genes
    nsv4583673copy number variation1nstd183human GRCh37 chr2: 264,001-264,879 , GRCh38.p12 chr2: 264,001-264,879 ACP1, SH3YL1
    nsv4583670copy number variation1nstd183human GRCh37 chr2: 262,759-264,852 , GRCh38.p12 chr2: 262,759-264,852 ACP1, SH3YL1
    nsv4454966copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,770-7,502,796 , GRCh38.p12 chr2: 12,770-7,362,665 LINC01810, ADI1, 83 more genes
    nsv4453225copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-2,832,894 , GRCh38.p12 chr2: 12,770-2,829,122 LOC105373359, LOC107985839, 29 more genes
    nsv4452632copy number variation1nstd102humanUncertain significance GRCh37 chr2: 12,770-3,819,558 , GRCh38.p12 chr2: 12,770-3,771,968 LOC107985838, LOC100996637, 45 more genes
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