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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964240insertion1nstd209human GRCh38 chr9: 97,362,672-97,362,672 , GRCh37.p13 chr9: 100,124,954-100,124,954 SUGT1P4-STRA6LP-CCDC180, MIR1302-8, 1 more genes
    nsv5708108mobile element insertion2nstd211human GRCh38 chr9: 97,362,681-97,362,681 , GRCh37.p13 chr9: 100,124,963-100,124,963 SUGT1P4-STRA6LP-CCDC180, MIR1302-8, 1 more genes
    nsv5633147insertion1nstd207human GRCh38 chr9: 97,362,666-97,362,666 , GRCh37.p13 chr9: 100,124,948-100,124,948 SUGT1P4-STRA6LP-CCDC180, MIR1302-8, 1 more genes
    nsv5492948copy number variation1nstd206human GRCh38 chr9: 97,318,864-97,340,961 , GRCh37.p13 chr9: 100,081,146-100,103,243 CCDC180, SUGT1P4-STRA6LP-CCDC180
    nsv5492554copy number variation1nstd206human GRCh38 chr9: 97,368,229-97,368,284 , GRCh37.p13 chr9: 100,130,511-100,130,566 CCDC180, SUGT1P4-STRA6LP-CCDC180
    nsv5490682copy number variation1nstd206human GRCh38 chr9: 97,331,437-97,331,514 , GRCh37.p13 chr9: 100,093,719-100,093,796 CCDC180, SUGT1P4-STRA6LP-CCDC180
    nsv5474035copy number variation1nstd206human GRCh38 chr9: 97,367,270-97,367,337 , GRCh37.p13 chr9: 100,129,552-100,129,619 CCDC180, SUGT1P4-STRA6LP-CCDC180
    nsv5408473mobile element insertion1nstd206human GRCh38 chr9: 97,362,681-97,362,732 , GRCh37.p13 chr9: 100,124,963-100,125,014 SUGT1P4-STRA6LP-CCDC180, MIR1302-8, 1 more genes
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5130501mobile element insertion1nstd203human GRCh38 chr9: 97,362,666-97,362,681 , GRCh37.p13 chr9: 100,124,948-100,124,963 SUGT1P4-STRA6LP-CCDC180, MIR1302-8, 1 more genes
    nsv5128517mobile element insertion1nstd203human GRCh38 chr9: 97,362,673-97,362,681 , GRCh37.p13 chr9: 100,124,955-100,124,963 SUGT1P4-STRA6LP-CCDC180, MIR1302-8, 1 more genes
    nsv4982692copy number variation1nstd200human GRCh38 chr9: 97,357,001-97,360,687 , GRCh37.p13 chr9: 100,119,283-100,122,969 SUGT1P4-STRA6LP-CCDC180, CCDC180
    nsv4982691copy number variation1nstd200human GRCh38 chr9: 97,318,864-97,340,961 , GRCh37.p13 chr9: 100,081,146-100,103,243 CCDC180, SUGT1P4-STRA6LP-CCDC180
    nsv4824172copy number variation1nstd200human GRCh37 chr9: 100,081,146-100,103,243 , GRCh38.p12 chr9: 97,318,864-97,340,961 CCDC180, SUGT1P4-STRA6LP-CCDC180
    nsv4716663mobile element insertion1nstd186human GRCh38.p12 chr9: 97,362,666-97,362,666 , GRCh37 chr9: 100,124,948-100,124,948 SUGT1P4-STRA6LP-CCDC180, MIR1302-8, 1 more genes
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 MIR3074, LOC112268039, 108 more genes
    nsv4487059mobile element insertion1nstd166human GRCh37.p13 chr9: 100,124,948-100,124,948 , GRCh38.p12 chr9: 97,362,666-97,362,666 SUGT1P4-STRA6LP-CCDC180, MIR1302-8, 1 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
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