A Bhattacharya - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3882502	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 92,213,175-92,242,155 , GRCh37.p13 chr7: 91,842,489-91,871,469	KRIT1
nsv6312873	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,842,489-91,871,449 , GRCh38.p12 chr7: 92,213,175-92,242,135	KRIT1
nsv5673795	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,851,196-91,871,469 , GRCh38.p12 chr7: 92,221,882-92,242,155	KRIT1
nsv5673796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,863,743-91,871,469 , GRCh38.p12 chr7: 92,234,429-92,242,155	KRIT1
nsv3879427	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,863,763-91,871,451 , GRCh38.p12 chr7: 92,234,449-92,242,137	KRIT1
nsv5673852	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,866,961-91,871,469 , GRCh38.p12 chr7: 92,237,647-92,242,155	KRIT1
nsv3880387	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 92,240,973-92,242,155 , GRCh37 chr7: 91,870,287-91,871,469	KRIT1
nsv3878982	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 92,225,700-92,226,702 , GRCh37 chr7: 91,855,014-91,856,016	KRIT1
nsv6312463	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,842,489-91,843,313 , GRCh38.p12 chr7: 92,213,175-92,213,999	KRIT1
nsv6312361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,830,050-91,830,803 , GRCh38.p12 chr7: 92,200,736-92,201,489	KRIT1
nsv4682373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,863,743-91,864,257 , GRCh38.p12 chr7: 92,234,429-92,234,943	KRIT1
nsv997134	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 46,696,347-46,741,793 , GRCh38.p12 chrX: 46,836,912-46,882,358	RP2
nsv7093515	insertion	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,864,793-91,864,793 , GRCh38 chr7: 92,235,479-92,235,479	KRIT1
nsv7097644	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 91,851,196-91,852,312 , GRCh38.p12 chr7: 92,221,882-92,222,998	KRIT1
nsv3879736	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 91,864,697-91,867,093 , GRCh38 chr7: 92,235,383-92,237,779	KRIT1
nsv3871964	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 65,550,600-65,706,998 , GRCh38 chr6: 64,840,707-64,997,105	EYS, LOC105377837
nsv7098141	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,830,050-91,867,093 , GRCh38.p12 chr7: 92,200,736-92,237,779	KRIT1, MIR1285-1
nsv5673851	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,829,918-91,851,387 , GRCh38.p12 chr7: 92,200,604-92,222,073	MIR1285-1, KRIT1
nsv7097391	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,830,050-91,844,111 , GRCh38.p12 chr7: 92,200,736-92,214,797	KRIT1, MIR1285-1
nsv6312462	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 91,830,690-91,832,501 , GRCh38.p12 chr7: 92,201,376-92,203,187	MIR1285-1, KRIT1

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Number of Variants: 20

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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 23

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Number of Variants: 20

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Supplemental Content

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