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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099191copy number variation1nstd231human GRCh38.p12 chr1: 29,821,343-31,198,272 , GRCh37 chr1: 30,294,190-31,671,119 MATN1, LAPTM5, 21 more genes
    nsv7057808inversion1nstd229human GRCh38 chr1: 30,746,264-30,750,183 , GRCh37.p13 chr1: 31,219,111-31,223,030 LOC105378620, LAPTM5
    nsv7054772inversion1nstd229human GRCh38 chr1: 30,746,134-30,751,231 , GRCh37.p13 chr1: 31,218,981-31,224,078 LAPTM5, LOC105378620
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648610copy number variation1nstd229human GRCh38 chr1: 30,739,937-30,741,639 , GRCh37.p13 chr1: 31,212,784-31,214,486 LAPTM5
    nsv6648609copy number variation1nstd229human GRCh38 chr1: 30,735,263-30,737,601 , GRCh37.p13 chr1: 31,208,110-31,210,448 LAPTM5, MIR4420
    nsv6648608copy number variation1nstd229human GRCh38 chr1: 30,712,815-30,848,383 , GRCh37.p13 chr1: 31,185,662-31,321,230 MIR4420, LOC105378620, 6 more genes
    nsv6648470copy number variation1nstd229human GRCh38 chr1: 30,747,974-30,749,893 , GRCh37.p13 chr1: 31,220,821-31,222,740 LOC105378620, LAPTM5
    nsv6648195copy number variation1nstd229human GRCh38 chr1: 30,730,092-30,751,334 , GRCh37.p13 chr1: 31,202,939-31,224,181 LAPTM5, MIR4420, 1 more genes
    nsv6626250copy number variation1nstd224human GRCh37 chr1: 31,148,956-31,247,236 , GRCh38.p12 chr1: 30,676,109-30,774,389 MATN1, LAPTM5, 4 more genes
    nsv6550622inversion1nstd223human GRCh38 chr1: 30,746,264-30,750,183 , GRCh37.p13 chr1: 31,219,111-31,223,030 LOC105378620, LAPTM5
    nsv6328254copy number variation1nstd223human GRCh38 chr1: 30,750,191-30,751,210 , GRCh37.p13 chr1: 31,223,038-31,224,057 LOC105378620, LAPTM5
    nsv6316978copy number variation1nstd223human GRCh38 chr1: 30,669,086-30,779,524 , GRCh37.p13 chr1: 31,141,933-31,252,371 MIR4420, LOC105378621, 4 more genes
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6155352copy number variation1nstd214human GRCh38 chr1: 30,732,165-30,732,331 , GRCh37.p13 chr1: 31,205,012-31,205,178 LAPTM5
    nsv6059994insertion1nstd212human GRCh38 chr1: 30,732,368-30,732,368 , GRCh37.p13 chr1: 31,205,215-31,205,215 LAPTM5
    nsv6053844insertion1nstd212human GRCh38 chr1: 30,732,260-30,732,260 , GRCh37.p13 chr1: 31,205,107-31,205,107 LAPTM5
    nsv6043678insertion1nstd212human GRCh38 chr1: 30,744,289-30,744,289 , GRCh37.p13 chr1: 31,217,136-31,217,136 LOC105378620, LAPTM5
    nsv5983818copy number variation1nstd212human GRCh38 chr1: 30,732,166-30,732,367 , GRCh37.p13 chr1: 31,205,013-31,205,214 LAPTM5
    nsv5983586copy number variation1nstd212human GRCh38 chr1: 30,209,364-32,642,526 , GRCh37.p13 chr1: 30,682,211-33,108,127 , HDAC1, 69 more genes
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