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Items: 1 to 20 of 299

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv5975553inversion1nstd209human GRCh38 chr9: 61,533,844-61,993,067 , GRCh37.p13 chr9: 44,741,682-45,697,082 , FAM27C, 9 more genes
    nsv5919501copy number variation1nstd209human GRCh38 chr9: 61,557,000-65,487,786 , GRCh37.p13 chr: NaN-NaN , MTCO1P36, 98 more genes
    nsv5918216copy number variation1nstd209human GRCh38 chr9: 61,647,960-65,578,967 , GRCh37.p13 chr: NaN-NaN , SDR42E1P3, 99 more genes
    nsv5914346copy number variation1nstd209human GRCh38 chr9: 60,768,680-66,674,368 , GRCh37.p13 chr: NaN-NaN , MEP1AP3, 146 more genes
    nsv5910323copy number variation1nstd209human GRCh38 chr9: 61,604,972-65,538,433 , GRCh37.p13 chr: NaN-NaN , FAM242E, 98 more genes
    nsv5554508sequence alteration1nstd206human GRCh38 chr9: 39,866,147-63,791,228 , GRCh37.p13 chr9: 39,713,687-67,542,104 , PTGER4P2, 168 more genes
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4730187inversion17nstd198human GRCh38 chr9: 61,785,368-62,487,139 , GRCh37.p13 chr9: 44,960,294-46,798,440 , FGF7P6, 17 more genes
    nsv4680877copy number variation1nstd189human GRCh37.p13 chr9: 43,635,114-66,323,059 , GRCh38.p12 chr9: 41,747,162-65,568,548 , IGKV1OR-2, 153 more genes
    nsv4680653copy number variation1nstd189human GRCh37.p13 chr9: 45,054,941-69,978,022 , GRCh38.p12 chr9: 41,747,162-65,568,548 , IGKV1OR-2, 153 more genes
    nsv4680342copy number variation1nstd189human GRCh37.p13 chr9: 43,315,671-65,672,607 , GRCh38.p12 chr9: 41,747,162-65,568,548 , IGKV1OR-2, 153 more genes
    nsv4679716copy number variation1nstd189human GRCh37.p13 chr9: 44,114,873-69,844,813 , GRCh38.p12 chr9: 40,711,180-67,920,552 , RBPJP2, 243 more genes
    nsv4679421copy number variation1nstd189human GRCh37.p13 chr9: 44,114,873-67,360,687 , GRCh38.p12 chr9: 41,747,162-65,568,548 , IGKV1OR-2, 153 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4673727copy number variation1nstd186human GRCh37 chr9: 38,997,411-46,584,047 , GRCh38.p12 chr9: 40,529,065-67,217,006 , LOC101929878, 232 more genes
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