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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052556inversion1nstd229human GRCh38 chr5: 170,680,318-170,680,378 , GRCh37.p13 chr5: 170,107,322-170,107,382 KCNIP1-AS1, KCNIP1
    nsv6791774copy number variation1nstd229human GRCh38 chr5: 170,668,019-170,674,219 , GRCh37.p13 chr5: 170,095,023-170,101,223 KCNIP1, KCNIP1-AS1
    nsv6790298copy number variation1nstd229human GRCh38 chr5: 170,642,011-170,653,896 , GRCh37.p13 chr5: 170,069,015-170,080,900 KCNIP1, KCNIP1-AS1
    nsv6784015copy number variation1nstd229human GRCh38 chr5: 170,680,176-170,680,226 , GRCh37.p13 chr5: 170,107,180-170,107,230 KCNIP1-AS1, KCNIP1
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6780290copy number variation1nstd229human GRCh38 chr5: 170,661,974-170,665,907 , GRCh37.p13 chr5: 170,088,978-170,092,911 KCNIP1, KCNIP1-AS1
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6636414copy number variation1nstd102humanUncertain significance GRCh37 chr5: 169,679,354-170,242,652 , GRCh38.p12 chr5: 170,252,350-170,815,648 GABRP, KCNIP1-OT1, 10 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 more genes
    nsv6135392copy number variation1nstd213human GRCh37 chr5: 169,960,000-170,570,001 , GRCh38.p12 chr5: 170,532,996-171,142,997 GABRP, KCNIP1, 7 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5471380copy number variation1nstd206human GRCh38 chr5: 170,679,398-170,680,153 , GRCh37.p13 chr5: 170,106,402-170,107,157 KCNIP1, KCNIP1-AS1
    nsv5463333copy number variation1nstd206human GRCh38 chr5: 170,667,144-170,669,825 , GRCh37.p13 chr5: 170,094,148-170,096,829 KCNIP1-AS1, KCNIP1
    nsv5460971copy number variation1nstd206human GRCh38 chr5: 170,655,285-170,655,345 , GRCh37.p13 chr5: 170,082,289-170,082,349 KCNIP1, KCNIP1-AS1
    nsv4949213copy number variation1nstd200human GRCh38 chr5: 170,677,545-170,700,520 , GRCh37.p13 chr5: 170,104,549-170,127,524 KCNIP1-AS1, KCNIP1
    nsv4729368copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 166,378,793-170,174,830 , GRCh38.p12 chr5: 166,951,788-170,747,826 DOCK2, FOXI1, 38 more genes
    nsv4597888copy number variation1nstd183human GRCh37 chr5: 170,063,238-170,780,570 , GRCh38.p12 chr5: 170,636,234-171,353,566 LOC107986474, GABRP, 10 more genes
    nsv4592792copy number variation1nstd183human GRCh37 chr5: 170,063,076-170,777,960 , GRCh38.p12 chr5: 170,636,072-171,350,956 KCNIP1, LOC107986473, 10 more genes
    nsv4590472copy number variation1nstd183human GRCh37 chr5: 170,094,232-170,096,729 , GRCh38.p12 chr5: 170,667,228-170,669,725 KCNIP1, KCNIP1-AS1
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