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Items: 1 to 20 of 769

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6128427insertion1nstd186human GRCh37 chrX: 154,984,786-154,984,790 , GRCh38.p12 chrX: 155,755,124-155,755,128 SPRY3
    nsv6113050copy number variation1nstd186human GRCh37 chrX: 154,918,460-154,921,743 , GRCh38.p12 chrX: 155,688,799-155,692,082 SPRY3
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5979819copy number variation1nstd209human GRCh38 chrX: 155,645,289-155,656,497 , GRCh37.p13 chrX: 154,874,950-154,886,158 , GRCh37.p13 chrX|NW_003871103.3: 3,079,268-3,090,476 SPRY3
    nsv5979347copy number variation1nstd209human GRCh38 chrX: 155,676,884-155,686,629 , GRCh37.p13 chrX: 154,906,586-154,916,290 SPRY3
    nsv5979050copy number variation1nstd209human GRCh38 chrX: 155,638,223-155,641,398 , GRCh37.p13 chrX|NW_003871103.3: 3,072,202-3,075,377 , GRCh37.p13 chrX: 154,867,884-154,871,059 SPRY3
    nsv5978741copy number variation2nstd209human GRCh38 chrX: 155,685,330-155,688,729 , GRCh37.p13 chrX: 154,914,991-154,918,390 SPRY3
    nsv5978278copy number variation2nstd209human GRCh38 chrX: 155,775,416-155,779,877 , GRCh37.p13 chrX: 155,005,078-155,009,539 SPRY3
    nsv5978234copy number variation1nstd209human GRCh38 chrX: 155,642,289-155,653,598 , GRCh37.p13 chrX: 154,871,950-154,883,259 , GRCh37.p13 chrX|NW_003871103.3: 3,076,268-3,087,577 SPRY3
    nsv5976494copy number variation2nstd209human GRCh38 chrX: 155,724,671-155,736,709 , GRCh37.p13 chrX: 154,954,333-154,966,371 SPRY3
    nsv5976123copy number variation1nstd209human GRCh38 chrX: 155,632,559-155,637,922 , GRCh37.p13 chrX|NW_003871103.3: 3,066,538-3,071,901 , GRCh37.p13 chrX: 154,862,220-154,867,583 SPRY3
    nsv5975590copy number variation2nstd209human GRCh38 chrX: 155,762,484-155,768,405 , GRCh37.p13 chrX: 154,992,146-154,998,067 SPRY3
    nsv5975428copy number variation2nstd209human GRCh38 chrX: 155,692,030-155,699,491 , GRCh37.p13 chrX: 154,921,691-154,929,152 SPRY3
    nsv5974088copy number variation2nstd209human GRCh38 chrX: 155,745,535-155,764,083 , GRCh37.p13 chrX: 154,975,197-154,993,745 SPRY3
    nsv5973779copy number variation2nstd209human GRCh38 chrX: 155,778,278-155,787,610 , GRCh37.p13 chrX: 155,007,940-155,017,272 SPRY3
    nsv5973572copy number variation1nstd209human GRCh38 chrX: 155,633,459-155,639,398 , GRCh37.p13 chrX|NW_003871103.3: 3,067,438-3,073,377 , GRCh37.p13 chrX: 154,863,120-154,869,059 SPRY3
    nsv5972828copy number variation1nstd209human GRCh38 chrX: 155,621,239-155,623,588 , GRCh37.p13 chrX|NW_003871103.3: 3,055,218-3,057,567 , GRCh37.p13 chrX: 154,850,900-154,853,249 SPRY3
    nsv5972624copy number variation1nstd209human GRCh38 chrX: 155,616,462-155,623,588 , GRCh37.p13 chrX|NW_003871103.3: 3,050,441-3,057,567 , GRCh37.p13 chrX: 154,846,123-154,853,249 SPRY3
    nsv5971074copy number variation1nstd209human GRCh38 chrX: 155,688,930-155,692,029 , GRCh37.p13 chrX: 154,918,591-154,921,690 SPRY3
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