Fletcher factor - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7093216	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 154,931,495-154,990,580 , GRCh37.p13 chrX\|NW_003871103.3: 2,365,474-2,424,559 , GRCh37.p13 chrX: 154,159,770-154,218,855	F8
nsv7093063	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 154,969,553-155,022,724 , GRCh37.p13 chrX\|NW_003871103.3: 2,403,532-2,456,703 , GRCh37.p13 chrX: 154,197,828-154,250,999	F8
nsv4450811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 138,612,860-138,645,598 , GRCh38 chrX: 139,530,701-139,563,439	F9
nsv3881674	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 139,530,759-139,562,076 , GRCh37 chrX: 138,612,918-138,644,235	F9
nsv4681108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 138,623,208-138,645,598 , GRCh38.p12 chrX: 139,541,049-139,563,439	F9
nsv7093173	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 154,974,508-154,986,431 , GRCh37.p13 chrX\|NW_003871103.3: 2,408,487-2,420,410 , GRCh37.p13 chrX: 154,202,783-154,214,706	F8
nsv7093099	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 154,986,438-154,997,956 , GRCh37.p13 chrX\|NW_003871103.3: 2,420,417-2,431,935 , GRCh37.p13 chrX: 154,214,713-154,226,231	F8
nsv7137181	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 138,612,923-138,623,234 , GRCh38.p12 chrX: 139,530,764-139,541,075	F9
nsv7137189	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 139,530,738-139,537,009 , GRCh37.p13 chrX: 138,612,897-138,619,168	F9
nsv7093208	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 154,959,165-154,963,500 , GRCh37.p13 chrX\|NW_003871103.3: 2,393,144-2,397,479 , GRCh37.p13 chrX: 154,187,440-154,191,775	F8
nsv7093071	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 154,930,804-154,933,516 , GRCh37.p13 chrX\|NW_003871103.3: 2,364,783-2,367,495 , GRCh37.p13 chrX: 154,159,079-154,161,791	F8
nsv7093115	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 154,835,791-154,837,753 , GRCh37.p13 chrX\|NW_003871103.3: 2,269,770-2,271,732 , GRCh37.p13 chrX: 154,064,066-154,066,028	F8
nsv7093032	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 155,022,409-155,022,724 , GRCh37.p13 chrX\|NW_003871103.3: 2,456,388-2,456,703 , GRCh37.p13 chrX: 154,250,684-154,250,999	F8
nsv5673906	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 138,612,860-138,613,021 , GRCh38.p12 chrX: 139,530,701-139,530,862	F9
nsv7137022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 154,173,409-154,173,410 , GRCh38 chrX: 154,945,134-154,945,135	F8
nsv7093564	insertion	1	nstd102	human	Pathogenic	GRCh37 chrX: 138,630,538-138,630,538 , GRCh38 chrX: 139,548,379-139,548,379	F9
nsv6315586	delins	1	nstd102	human	Pathogenic	GRCh37 chrX: 138,623,347-138,627,796 , GRCh38 chrX: 139,541,188-139,545,637	F9
nsv7137217	delins	1	nstd102	human	Pathogenic	GRCh37 chrX: 154,133,219-154,133,522 , GRCh38 chrX: 154,904,944-154,905,247	F8
nsv5673836	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 154,159,808-154,166,711 , GRCh38 chrX: 154,931,533-154,938,436	F8
nsv4458038	complex substitution	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 154,156,796-154,227,925 , GRCh38.p12 chrX: 154,928,521-154,999,650	F8

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Send to:

Search results

Items: 1 to 20 of 28

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 28

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity