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Items: 1 to 20 of 98

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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
    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
    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
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv3922790copy number variation1nstd102humanPathogenic GRCh38 chr9: 94,713,892-98,121,186 , GRCh37 chr9: 97,476,174-100,883,468 , NCBI36 chr9: 96,515,995-99,923,289 CDC14B, PTCH1, 87 more genes
    nsv3922685copy number variation1nstd102humanPathogenic GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076 MUSK, LOC105376176, 464 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3922551copy number variation1nstd102humanPathogenic GRCh38 chr9: 95,061,030-108,695,569 , NCBI36 chr9: 96,863,133-110,497,670 , GRCh37 chr9: 97,823,312-111,457,849 HEMGN, LOC105376183, 243 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
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